{"id":23974,"date":"2022-08-06T15:39:48","date_gmt":"2022-08-06T19:39:48","guid":{"rendered":"https:\/\/hepatochem.com\/photoreacteurs-accessoires-led-et-plus-encore\/photoredox-box\/"},"modified":"2026-06-02T08:00:05","modified_gmt":"2026-06-02T12:00:05","slug":"photoredox-box","status":"publish","type":"page","link":"https:\/\/hepatochem.com\/fr\/photoreacteurs-accessoires-led-et-plus-encore\/photoredox-box\/","title":{"rendered":"PhotoRedOx Box&#x2122;"},"content":{"rendered":"<p>[et_pb_section fb_built=\u00a0\u00bb1&Prime; _builder_version=\u00a0\u00bb4.16&Prime; custom_padding=\u00a0\u00bb0|0px|0|0px|false|false\u00a0\u00bb global_colors_info=\u00a0\u00bb{}\u00a0\u00bb][et_pb_row _builder_version=\u00a0\u00bb4.20.4&Prime; width=\u00a0\u00bb100%\u00a0\u00bb custom_padding=\u00a0\u00bb0px|0px|0px|0px|false|false\u00a0\u00bb global_colors_info=\u00a0\u00bb{}\u00a0\u00bb][et_pb_column type=\u00a0\u00bb4_4&Prime; _builder_version=\u00a0\u00bb4.16&Prime; custom_padding=\u00a0\u00bb|||\u00a0\u00bb global_colors_info=\u00a0\u00bb{}\u00a0\u00bb custom_padding__hover=\u00a0\u00bb|||\u00a0\u00bb][et_pb_text _builder_version=\u00a0\u00bb4.27.2&Prime; text_font=\u00a0\u00bb||||||||\u00a0\u00bb text_line_height=\u00a0\u00bb2em\u00a0\u00bb header_font=\u00a0\u00bb|700|||||||\u00a0\u00bb header_4_line_height=\u00a0\u00bb2em\u00a0\u00bb custom_margin=\u00a0\u00bb0px|15px|0px|15px|false|false\u00a0\u00bb global_colors_info=\u00a0\u00bb{}\u00a0\u00bb]<\/p>\n<h4 style=\"text-align: left;\"><strong>La PhotoRedOx Box&#x2122; d\u2019EvoluChem est le photor\u00e9acteur de photochimie de choix pour le chimiste qui cherche \u00e0 standardiser les installations photochimiques de laboratoire de mani\u00e8re \u00e9conomique. Sa conception flexible permet l\u2019utilisation de LED interchangeables de 365 nm \u00e0 808 nm et d\u2019une grande vari\u00e9t\u00e9 de flacons. <\/strong><\/h4>\n<p style=\"text-align: left;\">Ce photor\u00e9acteur de photochimie (brevet am\u00e9ricain n\u00b0 10\u202f906\u202f022) est con\u00e7u pour faciliter l\u2019exp\u00e9rimentation photochimique. Il est compatible avec la plupart des formats de flacons (flacons de 0,3 ml, 2 ml, 4 ml et 20 ml) et sa conception compacte permet de l\u2019utiliser avec n\u2019importe quel agitateur magn\u00e9tique. Un ventilateur int\u00e9gr\u00e9 maintient les conditions de r\u00e9action \u00e0 temp\u00e9rature ambiante.  <\/p>\n<p>[\/et_pb_text][et_pb_image src=\u00a0\u00bbhttps:\/\/hepatochem.com\/wp-content\/uploads\/2026\/04\/photobox-gray-citation-500.png\u00a0\u00bb alt=\u00a0\u00bbphotoredox box\u00a0\u00bb title_text=\u00a0\u00bbphotoredox box\u00a0\u00bb _builder_version=\u00a0\u00bb4.27.6&Prime; _module_preset=\u00a0\u00bbdefault\u00a0\u00bb max_width=\u00a0\u00bb49%\u00a0\u00bb module_alignment=\u00a0\u00bbcenter\u00a0\u00bb custom_margin=\u00a0\u00bb|0px||0px|false|false\u00a0\u00bb custom_padding=\u00a0\u00bb|15px||15px|false|true\u00a0\u00bb global_colors_info=\u00a0\u00bb{}\u00a0\u00bb][\/et_pb_image][et_pb_button button_url=\u00a0\u00bbhttps:\/\/hepatochem.com\/photoreactor-order\/\u00a0\u00bb button_text=\u00a0\u00bbCommande et tarifs ici\u00a0\u00bb button_alignment=\u00a0\u00bbcenter\u00a0\u00bb _builder_version=\u00a0\u00bb4.20.4&Prime; _module_preset=\u00a0\u00bbdefault\u00a0\u00bb custom_margin=\u00a0\u00bb||3px|||\u00a0\u00bb global_colors_info=\u00a0\u00bb{}\u00a0\u00bb][\/et_pb_button][\/et_pb_column][\/et_pb_row][et_pb_row column_structure=\u00a0\u00bb3_5,2_5&Prime; _builder_version=\u00a0\u00bb4.20.4&Prime; width=\u00a0\u00bb100%\u00a0\u00bb custom_padding=\u00a0\u00bb30px|0px|27px|0px|false|false\u00a0\u00bb global_colors_info=\u00a0\u00bb{}\u00a0\u00bb][et_pb_column type=\u00a0\u00bb3_5&Prime; _builder_version=\u00a0\u00bb4.16&Prime; custom_padding=\u00a0\u00bb|||\u00a0\u00bb global_colors_info=\u00a0\u00bb{}\u00a0\u00bb custom_padding__hover=\u00a0\u00bb|||\u00a0\u00bb][et_pb_blurb title=\u00a0\u00bbCaract\u00e9ristiques\u00a0\u00bb _builder_version=\u00a0\u00bb4.20.4&Prime; header_level=\u00a0\u00bbh3&Prime; header_font=\u00a0\u00bb|700|||||||\u00a0\u00bb header_font_size=\u00a0\u00bb20px\u00a0\u00bb body_font=\u00a0\u00bb||||||||\u00a0\u00bb custom_padding=\u00a0\u00bb|15px|0px|15px|false|true\u00a0\u00bb global_colors_info=\u00a0\u00bb{}\u00a0\u00bb]<\/p>\n<ul>\n<li style=\"list-style-type: none;\">\n<ul>\n<li>Plusieurs sources lumineuses disponibles de 365 nm \u00e0 808 nm<\/li>\n<li>Chambre de photochimie pour optimiser l\u2019intensit\u00e9 lumineuse<\/li>\n<li>Format de flacons flexible<\/li>\n<li>Agitation magn\u00e9tique sur agitateur standard<\/li>\n<li>Refroidissement par ventilateur pour maintenir l\u2019exp\u00e9rience \u00e0 temp\u00e9rature ambiante<\/li>\n<li>Gamme pr\u00e9-con\u00e7ue de catalyseurs et de r\u00e9actifs disponible<\/li>\n<li>Pour plus d\u2019efficacit\u00e9, d\u00e9couvrez l\u2019accessoire <a href=\"https:\/\/hepatochem.com\/photoreactors-leds-accessories\/photoredox-flow-reactor\/\">PhotoRedOx Flow Reactor<\/a><\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p>[\/et_pb_blurb][et_pb_blurb title=\u00a0\u00bbAvantages\u00a0\u00bb _builder_version=\u00a0\u00bb4.20.4&Prime; header_level=\u00a0\u00bbh3&Prime; header_font=\u00a0\u00bb|700|||||||\u00a0\u00bb header_text_align=\u00a0\u00bbleft\u00a0\u00bb header_font_size=\u00a0\u00bb20px\u00a0\u00bb body_font=\u00a0\u00bb||||||||\u00a0\u00bb custom_margin=\u00a0\u00bb-15px||-7px|||\u00a0\u00bb custom_padding=\u00a0\u00bb|15px||15px|false|true\u00a0\u00bb global_colors_info=\u00a0\u00bb{}\u00a0\u00bb]<\/p>\n<ul>\n<li style=\"list-style-type: none;\">\n<ul>\n<li><span>Installation facile sur un agitateur standard<\/span><\/li>\n<li><span>R\u00e9alisez jusqu\u2019\u00e0 32 conditions de r\u00e9action simultan\u00e9ment<\/span><\/li>\n<li><span>Les flacons scell\u00e9s individuellement permettent une conception d\u2019\u00e9tude flexible<\/span><\/li>\n<li><span>\u00c9conomisez votre substrat en utilisant des conditions de r\u00e9action \u00e0 petite \u00e9chelle<\/span><\/li>\n<li><span>Gagnez du temps sur l\u2019optimisation<\/span><\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p>[\/et_pb_blurb][et_pb_video src=\u00a0\u00bbhttps:\/\/youtu.be\/JTEza4SbtDk?si=2tvYG_r4nLCoulzd\u00a0\u00bb _builder_version=\u00a0\u00bb4.27.4&Prime; _module_preset=\u00a0\u00bbdefault\u00a0\u00bb global_colors_info=\u00a0\u00bb{}\u00a0\u00bb][\/et_pb_video][\/et_pb_column][et_pb_column type=\u00a0\u00bb2_5&Prime; _builder_version=\u00a0\u00bb4.16&Prime; custom_padding=\u00a0\u00bb|||\u00a0\u00bb global_colors_info=\u00a0\u00bb{}\u00a0\u00bb custom_padding__hover=\u00a0\u00bb|||\u00a0\u00bb][et_pb_blurb title=\u00a0\u00bbAppareil avec source de lumi\u00e8re bleue\u00a0\u00bb image=\u00a0\u00bbhttps:\/\/hepatochem.com\/wp-content\/uploads\/2024\/07\/photobox-web3.png\u00a0\u00bb alt=\u00a0\u00bbphotor\u00e9acteur\u00a0\u00bb image_icon_width=\u00a0\u00bb100%\u00a0\u00bb _builder_version=\u00a0\u00bb4.20.4&Prime; header_level=\u00a0\u00bbh5&Prime; header_font=\u00a0\u00bb|700|||||||\u00a0\u00bb header_text_align=\u00a0\u00bbcenter\u00a0\u00bb width=\u00a0\u00bb100%\u00a0\u00bb max_width=\u00a0\u00bb100%\u00a0\u00bb max_height=\u00a0\u00bb100%\u00a0\u00bb custom_padding=\u00a0\u00bb|15px||15px|false|true\u00a0\u00bb global_colors_info=\u00a0\u00bb{}\u00a0\u00bb]<\/p>\n<p style=\"text-align: center;\"><span>HCK1006-01-016<\/span><br \/><span style=\"font-size: 12px; margin-top: -12px;\">(Brevet US n\u00b0 10\u202f906\u202f022)<\/span><\/p>\n<p>[\/et_pb_blurb][et_pb_blurb image=\u00a0\u00bbhttps:\/\/hepatochem.com\/wp-content\/uploads\/2016\/12\/light_mirrors-e1549406845169.png\u00a0\u00bb _builder_version=\u00a0\u00bb4.20.4&Prime; _module_preset=\u00a0\u00bbdefault\u00a0\u00bb max_width=\u00a0\u00bb100%\u00a0\u00bb custom_margin=\u00a0\u00bb|15px||15px|false|false\u00a0\u00bb custom_margin_tablet=\u00a0\u00bb|15px||15px|false|false\u00a0\u00bb custom_margin_phone=\u00a0\u00bb|0px||0px|false|true\u00a0\u00bb custom_margin_last_edited=\u00a0\u00bbon|phone\u00a0\u00bb custom_padding=\u00a0\u00bb|15px||15px|false|true\u00a0\u00bb global_colors_info=\u00a0\u00bb{}\u00a0\u00bb]<\/p>\n<p style=\"text-align: center;\"><strong>Conception unique<\/strong><strong><\/strong><\/p>\n<p>[\/et_pb_blurb][\/et_pb_column][\/et_pb_row][et_pb_row _builder_version=\u00a0\u00bb4.27.4&Prime; width=\u00a0\u00bb100%\u00a0\u00bb module_alignment=\u00a0\u00bbcenter\u00a0\u00bb custom_margin=\u00a0\u00bb|0px||0px|false|true\u00a0\u00bb global_colors_info=\u00a0\u00bb{}\u00a0\u00bb][et_pb_column type=\u00a0\u00bb4_4&Prime; _builder_version=\u00a0\u00bb4.16&Prime; custom_padding=\u00a0\u00bb|||\u00a0\u00bb global_colors_info=\u00a0\u00bb{}\u00a0\u00bb custom_padding__hover=\u00a0\u00bb|||\u00a0\u00bb][et_pb_text _builder_version=\u00a0\u00bb4.20.4&Prime; header_3_font=\u00a0\u00bb|700|||||||\u00a0\u00bb header_3_text_align=\u00a0\u00bbleft\u00a0\u00bb custom_padding=\u00a0\u00bb|15px||15px|false|true\u00a0\u00bb global_colors_info=\u00a0\u00bb{}\u00a0\u00bb]<\/p>\n<h3 style=\"text-align: left;\">Installation facile et conception compacte<\/h3>\n<p>[\/et_pb_text][et_pb_image src=\u00a0\u00bbhttps:\/\/hepatochem.com\/wp-content\/uploads\/2023\/08\/photobox-web-4-2.png\u00a0\u00bb alt=\u00a0\u00bbphotor\u00e9acteur\u00a0\u00bb title_text=\u00a0\u00bbphotobox web 4-2&Prime; align=\u00a0\u00bbcenter\u00a0\u00bb _builder_version=\u00a0\u00bb4.27.4&Prime; _module_preset=\u00a0\u00bbdefault\u00a0\u00bb width=\u00a0\u00bb100%\u00a0\u00bb max_width=\u00a0\u00bb100%\u00a0\u00bb module_alignment=\u00a0\u00bbcenter\u00a0\u00bb custom_margin=\u00a0\u00bb|0px||0px|false|true\u00a0\u00bb custom_margin_tablet=\u00a0\u00bb|15px||15px|false|false\u00a0\u00bb custom_margin_phone=\u00a0\u00bb|0px||0px|false|true\u00a0\u00bb custom_margin_last_edited=\u00a0\u00bbon|phone\u00a0\u00bb custom_padding=\u00a0\u00bb|15px||15px|false|true\u00a0\u00bb custom_padding_tablet=\u00a0\u00bb|0px||0px|false|false\u00a0\u00bb custom_padding_phone=\u00a0\u00bb|15px||15px|false|true\u00a0\u00bb custom_padding_last_edited=\u00a0\u00bbon|phone\u00a0\u00bb global_colors_info=\u00a0\u00bb{}\u00a0\u00bb][\/et_pb_image][\/et_pb_column][\/et_pb_row][et_pb_row _builder_version=\u00a0\u00bb4.20.4&Prime; width=\u00a0\u00bb100%\u00a0\u00bb custom_padding=\u00a0\u00bb|15px||15px|false|true\u00a0\u00bb global_colors_info=\u00a0\u00bb{}\u00a0\u00bb][et_pb_column type=\u00a0\u00bb4_4&Prime; _builder_version=\u00a0\u00bb4.16&Prime; custom_padding=\u00a0\u00bb|||\u00a0\u00bb global_colors_info=\u00a0\u00bb{}\u00a0\u00bb custom_padding__hover=\u00a0\u00bb|||\u00a0\u00bb][et_pb_text _builder_version=\u00a0\u00bb4.16&Prime; header_3_font=\u00a0\u00bb|700|||||||\u00a0\u00bb global_colors_info=\u00a0\u00bb{}\u00a0\u00bb]<\/p>\n<h3 style=\"text-align: left;\"><span>S\u2019adapte \u00e0 plusieurs tailles de flacons<\/span><\/h3>\n<p>[\/et_pb_text][\/et_pb_column][\/et_pb_row][et_pb_row column_structure=\u00a0\u00bb1_3,1_3,1_3&Prime; _builder_version=\u00a0\u00bb4.20.4&Prime; width=\u00a0\u00bb100%\u00a0\u00bb custom_padding=\u00a0\u00bb0|15px|0px|15px|false|true\u00a0\u00bb global_colors_info=\u00a0\u00bb{}\u00a0\u00bb][et_pb_column type=\u00a0\u00bb1_3&Prime; _builder_version=\u00a0\u00bb4.16&Prime; custom_padding=\u00a0\u00bb|||\u00a0\u00bb global_colors_info=\u00a0\u00bb{}\u00a0\u00bb custom_padding__hover=\u00a0\u00bb|||\u00a0\u00bb][et_pb_blurb title=\u00a0\u00bb32 flacons de 0,3 ml\u00a0\u00bb image=\u00a0\u00bbhttps:\/\/hepatochem.com\/wp-content\/uploads\/2019\/03\/IMG_3764-5.jpeg\u00a0\u00bb content_max_width=\u00a0\u00bb470px\u00a0\u00bb _builder_version=\u00a0\u00bb4.20.4&Prime; header_level=\u00a0\u00bbh6&Prime; header_font=\u00a0\u00bb|700|||||||\u00a0\u00bb header_text_align=\u00a0\u00bbcenter\u00a0\u00bb body_font_size=\u00a0\u00bb12px\u00a0\u00bb custom_padding=\u00a0\u00bb0px||\u00a0\u00bb global_colors_info=\u00a0\u00bb{}\u00a0\u00bb]<\/p>\n<p style=\"text-align: center;\">HCK1006-01-017<\/p>\n<p>[\/et_pb_blurb][\/et_pb_column][et_pb_column type=\u00a0\u00bb1_3&Prime; _builder_version=\u00a0\u00bb4.16&Prime; custom_padding=\u00a0\u00bb|||\u00a0\u00bb global_colors_info=\u00a0\u00bb{}\u00a0\u00bb custom_padding__hover=\u00a0\u00bb|||\u00a0\u00bb][et_pb_blurb title=\u00a0\u00bb8 flacons de 2 ml \u00a0\u00bb image=\u00a0\u00bbhttps:\/\/hepatochem.com\/wp-content\/uploads\/2019\/09\/2ml_holder_170x170.jpg\u00a0\u00bb _builder_version=\u00a0\u00bb4.20.4&Prime; header_level=\u00a0\u00bbh6&Prime; header_font=\u00a0\u00bb|700|||||||\u00a0\u00bb header_text_align=\u00a0\u00bbcenter\u00a0\u00bb body_font_size=\u00a0\u00bb12px\u00a0\u00bb custom_padding=\u00a0\u00bb0px||\u00a0\u00bb global_colors_info=\u00a0\u00bb{}\u00a0\u00bb]<\/p>\n<p style=\"text-align: center;\">HCK1006-01-018<\/p>\n<p>[\/et_pb_blurb][\/et_pb_column][et_pb_column type=\u00a0\u00bb1_3&Prime; _builder_version=\u00a0\u00bb4.16&Prime; custom_padding=\u00a0\u00bb|||\u00a0\u00bb global_colors_info=\u00a0\u00bb{}\u00a0\u00bb custom_padding__hover=\u00a0\u00bb|||\u00a0\u00bb][et_pb_blurb title=\u00a0\u00bb8 flacons de 4 ml<br \/>\n\u00a0\u00bb image=\u00a0\u00bbhttps:\/\/hepatochem.com\/wp-content\/uploads\/2019\/09\/4ml_holder_170x170.jpg\u00a0\u00bb _builder_version=\u00a0\u00bb4.20.4&Prime; header_level=\u00a0\u00bbh6&Prime; header_font=\u00a0\u00bb|700|||||||\u00a0\u00bb header_text_align=\u00a0\u00bbcenter\u00a0\u00bb body_font_size=\u00a0\u00bb12px\u00a0\u00bb custom_padding=\u00a0\u00bb0px|||0px\u00a0\u00bb global_colors_info=\u00a0\u00bb{}\u00a0\u00bb]<\/p>\n<p style=\"text-align: center;\">HCK1006-01-019<\/p>\n<p>[\/et_pb_blurb][\/et_pb_column][\/et_pb_row][et_pb_row column_structure=\u00a0\u00bb1_3,1_3,1_3&Prime; _builder_version=\u00a0\u00bb4.20.4&Prime; width=\u00a0\u00bb100%\u00a0\u00bb custom_padding=\u00a0\u00bb0|0px|0px|0px|false|false\u00a0\u00bb global_colors_info=\u00a0\u00bb{}\u00a0\u00bb][et_pb_column type=\u00a0\u00bb1_3&Prime; _builder_version=\u00a0\u00bb4.16&Prime; custom_padding=\u00a0\u00bb|||\u00a0\u00bb global_colors_info=\u00a0\u00bb{}\u00a0\u00bb custom_padding__hover=\u00a0\u00bb|||\u00a0\u00bb][et_pb_blurb title=\u00a0\u00bb8 flacons de 8 ml<br \/>\n\u00a0\u00bb image=\u00a0\u00bbhttps:\/\/hepatochem.com\/wp-content\/uploads\/2019\/09\/8ml_holder_170x170.jpg\u00a0\u00bb _builder_version=\u00a0\u00bb4.20.4&Prime; header_level=\u00a0\u00bbh6&Prime; header_font=\u00a0\u00bb|700|||||||\u00a0\u00bb header_text_align=\u00a0\u00bbcenter\u00a0\u00bb body_font_size=\u00a0\u00bb12px\u00a0\u00bb custom_padding=\u00a0\u00bb0px|||0px\u00a0\u00bb global_colors_info=\u00a0\u00bb{}\u00a0\u00bb]<\/p>\n<p style=\"text-align: center;\">HCK1006-01-020<\/p>\n<p>[\/et_pb_blurb][\/et_pb_column][et_pb_column type=\u00a0\u00bb1_3&Prime; _builder_version=\u00a0\u00bb4.16&Prime; custom_padding=\u00a0\u00bb|||\u00a0\u00bb global_colors_info=\u00a0\u00bb{}\u00a0\u00bb custom_padding__hover=\u00a0\u00bb|||\u00a0\u00bb][et_pb_blurb title=\u00a0\u00bb2 flacons de 20 ml<br \/>\n\u00a0\u00bb image=\u00a0\u00bbhttps:\/\/hepatochem.com\/wp-content\/uploads\/2019\/09\/20ml_holder_170x170.jpg\u00a0\u00bb _builder_version=\u00a0\u00bb4.20.4&Prime; header_level=\u00a0\u00bbh6&Prime; header_font=\u00a0\u00bb|700|||||||\u00a0\u00bb header_text_align=\u00a0\u00bbcenter\u00a0\u00bb body_font_size=\u00a0\u00bb12px\u00a0\u00bb custom_padding=\u00a0\u00bb0px|||0px\u00a0\u00bb global_colors_info=\u00a0\u00bb{}\u00a0\u00bb]<\/p>\n<p style=\"text-align: center;\">HCK1006-01-021<\/p>\n<p>[\/et_pb_blurb][\/et_pb_column][et_pb_column type=\u00a0\u00bb1_3&Prime; _builder_version=\u00a0\u00bb4.16&Prime; custom_padding=\u00a0\u00bb|||\u00a0\u00bb global_colors_info=\u00a0\u00bb{}\u00a0\u00bb custom_padding__hover=\u00a0\u00bb|||\u00a0\u00bb][et_pb_blurb title=\u00a0\u00bbCellule \u00e0 flux PFA de 2 ml\u00a0\u00bb image=\u00a0\u00bbhttps:\/\/hepatochem.com\/wp-content\/uploads\/2020\/09\/flow-reactor-e1662584276639.jpg\u00a0\u00bb alt=\u00a0\u00bbcellule \u00e0 flux\u00a0\u00bb _builder_version=\u00a0\u00bb4.27.6&Prime; header_level=\u00a0\u00bbh6&Prime; header_font=\u00a0\u00bb|700|||||||\u00a0\u00bb header_text_align=\u00a0\u00bbcenter\u00a0\u00bb body_font_size=\u00a0\u00bb12px\u00a0\u00bb custom_padding=\u00a0\u00bb0px|||0px\u00a0\u00bb global_colors_info=\u00a0\u00bb{}\u00a0\u00bb]<\/p>\n<p style=\"text-align: center;\">HCK1006-01-022<\/p>\n<p>[\/et_pb_blurb][\/et_pb_column][\/et_pb_row][et_pb_row _builder_version=\u00a0\u00bb4.27.0&Prime; _module_preset=\u00a0\u00bbdefault\u00a0\u00bb width=\u00a0\u00bb100%\u00a0\u00bb global_colors_info=\u00a0\u00bb{}\u00a0\u00bb][et_pb_column type=\u00a0\u00bb4_4&Prime; _builder_version=\u00a0\u00bb4.20.4&Prime; _module_preset=\u00a0\u00bbdefault\u00a0\u00bb global_colors_info=\u00a0\u00bb{}\u00a0\u00bb][et_pb_button button_url=\u00a0\u00bbhttps:\/\/hepatochem.com\/photoreactor-order\/\u00a0\u00bb button_text=\u00a0\u00bbCommande et tarifs ici\u00a0\u00bb button_alignment=\u00a0\u00bbcenter\u00a0\u00bb _builder_version=\u00a0\u00bb4.20.4&Prime; _module_preset=\u00a0\u00bbdefault\u00a0\u00bb global_colors_info=\u00a0\u00bb{}\u00a0\u00bb][\/et_pb_button][et_pb_contact_form email=\u00a0\u00bbcustomer.service@hepatochem.com\u00a0\u00bb title=\u00a0\u00bbRemplissez ce formulaire pour obtenir les tarifs et des informations\u00a0\u00bb custom_message=\u00a0\u00bbDemande au service client||et_pb_line_break_holder||||et_pb_line_break_holder||Page source : ||et_pb_line_break_holder||%%Products%%||et_pb_line_break_holder||||et_pb_line_break_holder||Nom : ||et_pb_line_break_holder||%%First_Name%% %%Last_Name%%||et_pb_line_break_holder||||et_pb_line_break_holder||Adresse e-mail : ||et_pb_line_break_holder||%%Email%%||et_pb_line_break_holder||||et_pb_line_break_holder||Soci\u00e9t\u00e9 : ||et_pb_line_break_holder||%%Company%%||et_pb_line_break_holder||||et_pb_line_break_holder||T\u00e9l\u00e9phone : ||et_pb_line_break_holder||%%Phone%%||et_pb_line_break_holder||||et_pb_line_break_holder||Ville : ||et_pb_line_break_holder||%%Location%%||et_pb_line_break_holder||||et_pb_line_break_holder||Pays :||et_pb_line_break_holder||%%Country%%||et_pb_line_break_holder||||et_pb_line_break_holder||Int\u00e9ress\u00e9 par les produits suivants :||et_pb_line_break_holder||||et_pb_line_break_holder||%%Products%%||et_pb_line_break_holder||||et_pb_line_break_holder||Produits d\u00e9couverts via :||et_pb_line_break_holder||%%source%%||et_pb_line_break_holder||||et_pb_line_break_holder||||et_pb_line_break_holder||Questions ou commentaires suppl\u00e9mentaires :||et_pb_line_break_holder||%%Questions%%\u00a0\u00bb use_redirect=\u00a0\u00bbon\u00a0\u00bb redirect_url=\u00a0\u00bbhttps:\/\/hepatochem.com\/photochemistry-starter-bundles-success\/?form=product\u00a0\u00bb submit_button_text=\u00a0\u00bbR\u00e9soudre et soumettre\u00a0\u00bb _builder_version=\u00a0\u00bb4.27.0&Prime; _module_preset=\u00a0\u00bbdefault\u00a0\u00bb _unique_id=\u00a0\u00bb2b472ac9-c451-4eba-b291-9e3ca7f600eb\u00a0\u00bb form_field_text_color=\u00a0\u00bb#6B6B6B\u00a0\u00bb form_field_focus_text_color=\u00a0\u00bb#000000&Prime; form_field_custom_margin=\u00a0\u00bbauto||||false|false\u00a0\u00bb title_level=\u00a0\u00bbh5&Prime; title_font=\u00a0\u00bb|600|||||||\u00a0\u00bb title_text_color=\u00a0\u00bb#00448B\u00a0\u00bb title_font_size=\u00a0\u00bb13px\u00a0\u00bb title_line_height=\u00a0\u00bb1.2em\u00a0\u00bb captcha_font=\u00a0\u00bb|700|||||||\u00a0\u00bb captcha_text_color=\u00a0\u00bb#8F8F8F\u00a0\u00bb captcha_letter_spacing=\u00a0\u00bb4px\u00a0\u00bb captcha_line_height=\u00a0\u00bb1em\u00a0\u00bb form_field_font=\u00a0\u00bb|600|||||||\u00a0\u00bb form_field_text_align=\u00a0\u00bbleft\u00a0\u00bb form_field_line_height=\u00a0\u00bb1em\u00a0\u00bb background_color=\u00a0\u00bbrgba(251,255,237,0)\u00a0\u00bb custom_button=\u00a0\u00bbon\u00a0\u00bb button_text_size=\u00a0\u00bb16px\u00a0\u00bb button_text_color=\u00a0\u00bb#FFFFFF\u00a0\u00bb button_bg_color=\u00a0\u00bb#8F8F8F\u00a0\u00bb button_border_width=\u00a0\u00bb0px\u00a0\u00bb button_border_color=\u00a0\u00bbRGBA(255,255,255,0)\u00a0\u00bb button_border_radius=\u00a0\u00bb30px\u00a0\u00bb button_font=\u00a0\u00bb|600|||||||\u00a0\u00bb button_icon=\u00a0\u00bb&#x35;||divi||400&Prime; button_icon_color=\u00a0\u00bb#FFFFFF\u00a0\u00bb button_on_hover=\u00a0\u00bboff\u00a0\u00bb button_custom_margin=\u00a0\u00bbauto|auto|auto|auto|true|true\u00a0\u00bb button_custom_padding=\u00a0\u00bb||||true|true\u00a0\u00bb text_orientation=\u00a0\u00bbleft\u00a0\u00bb custom_margin=\u00a0\u00bb5px|0px||0px|false|true\u00a0\u00bb custom_padding=\u00a0\u00bb|15px||15px|false|true\u00a0\u00bb custom_css_contact_fields=\u00a0\u00bb||||\u00a0\u00bb custom_css_captcha_label=\u00a0\u00bb  margin-right: 40px;||  margin-top: 20px;||\u00a0\u00bb border_width_all=\u00a0\u00bb1px\u00a0\u00bb border_color_all=\u00a0\u00bb#8F8F8F\u00a0\u00bb global_colors_info=\u00a0\u00bb{}\u00a0\u00bb][et_pb_contact_field field_id=\u00a0\u00bbFirst_Name\u00a0\u00bb field_title=\u00a0\u00bbPr\u00e9nom *\u00a0\u00bb _builder_version=\u00a0\u00bb4.20.0&Prime; background_color=\u00a0\u00bbRGBA(255,255,255,0)\u00a0\u00bb background_enable_color=\u00a0\u00bbon\u00a0\u00bb global_colors_info=\u00a0\u00bb{}\u00a0\u00bb button_text_size__hover_enabled=\u00a0\u00bboff\u00a0\u00bb button_one_text_size__hover_enabled=\u00a0\u00bboff\u00a0\u00bb button_two_text_size__hover_enabled=\u00a0\u00bboff\u00a0\u00bb button_text_color__hover_enabled=\u00a0\u00bboff\u00a0\u00bb button_one_text_color__hover_enabled=\u00a0\u00bboff\u00a0\u00bb button_two_text_color__hover_enabled=\u00a0\u00bboff\u00a0\u00bb button_border_width__hover_enabled=\u00a0\u00bboff\u00a0\u00bb button_one_border_width__hover_enabled=\u00a0\u00bboff\u00a0\u00bb button_two_border_width__hover_enabled=\u00a0\u00bboff\u00a0\u00bb button_border_color__hover_enabled=\u00a0\u00bboff\u00a0\u00bb button_one_border_color__hover_enabled=\u00a0\u00bboff\u00a0\u00bb button_two_border_color__hover_enabled=\u00a0\u00bboff\u00a0\u00bb button_border_radius__hover_enabled=\u00a0\u00bboff\u00a0\u00bb button_one_border_radius__hover_enabled=\u00a0\u00bboff\u00a0\u00bb button_two_border_radius__hover_enabled=\u00a0\u00bboff\u00a0\u00bb button_letter_spacing__hover_enabled=\u00a0\u00bboff\u00a0\u00bb button_one_letter_spacing__hover_enabled=\u00a0\u00bboff\u00a0\u00bb button_two_letter_spacing__hover_enabled=\u00a0\u00bboff\u00a0\u00bb button_bg_color__hover_enabled=\u00a0\u00bboff\u00a0\u00bb button_one_bg_color__hover_enabled=\u00a0\u00bboff\u00a0\u00bb button_two_bg_color__hover_enabled=\u00a0\u00bboff\u00a0\u00bb][\/et_pb_contact_field][et_pb_contact_field field_id=\u00a0\u00bbLast_Name\u00a0\u00bb field_title=\u00a0\u00bbNom *\u00a0\u00bb required_mark=\u00a0\u00bboff\u00a0\u00bb _builder_version=\u00a0\u00bb4.20.0&Prime; _module_preset=\u00a0\u00bbdefault\u00a0\u00bb form_field_text_color=\u00a0\u00bb#6B6B6B\u00a0\u00bb form_field_focus_text_color=\u00a0\u00bb#000000&Prime; form_field_text_align=\u00a0\u00bbleft\u00a0\u00bb global_colors_info=\u00a0\u00bb{}\u00a0\u00bb][\/et_pb_contact_field][et_pb_contact_field field_id=\u00a0\u00bbEmail\u00a0\u00bb field_title=\u00a0\u00bbAdresse e-mail *\u00a0\u00bb field_type=\u00a0\u00bbemail\u00a0\u00bb _builder_version=\u00a0\u00bb4.19.5&Prime; global_colors_info=\u00a0\u00bb{}\u00a0\u00bb button_text_size__hover_enabled=\u00a0\u00bboff\u00a0\u00bb button_one_text_size__hover_enabled=\u00a0\u00bboff\u00a0\u00bb button_two_text_size__hover_enabled=\u00a0\u00bboff\u00a0\u00bb button_text_color__hover_enabled=\u00a0\u00bboff\u00a0\u00bb button_one_text_color__hover_enabled=\u00a0\u00bboff\u00a0\u00bb button_two_text_color__hover_enabled=\u00a0\u00bboff\u00a0\u00bb button_border_width__hover_enabled=\u00a0\u00bboff\u00a0\u00bb button_one_border_width__hover_enabled=\u00a0\u00bboff\u00a0\u00bb button_two_border_width__hover_enabled=\u00a0\u00bboff\u00a0\u00bb button_border_color__hover_enabled=\u00a0\u00bboff\u00a0\u00bb button_one_border_color__hover_enabled=\u00a0\u00bboff\u00a0\u00bb button_two_border_color__hover_enabled=\u00a0\u00bboff\u00a0\u00bb button_border_radius__hover_enabled=\u00a0\u00bboff\u00a0\u00bb button_one_border_radius__hover_enabled=\u00a0\u00bboff\u00a0\u00bb button_two_border_radius__hover_enabled=\u00a0\u00bboff\u00a0\u00bb button_letter_spacing__hover_enabled=\u00a0\u00bboff\u00a0\u00bb button_one_letter_spacing__hover_enabled=\u00a0\u00bboff\u00a0\u00bb button_two_letter_spacing__hover_enabled=\u00a0\u00bboff\u00a0\u00bb button_bg_color__hover_enabled=\u00a0\u00bboff\u00a0\u00bb button_one_bg_color__hover_enabled=\u00a0\u00bboff\u00a0\u00bb button_two_bg_color__hover_enabled=\u00a0\u00bboff\u00a0\u00bb][\/et_pb_contact_field][et_pb_contact_field field_id=\u00a0\u00bbCompany\u00a0\u00bb field_title=\u00a0\u00bbEntreprise\/Affiliation *\u00a0\u00bb _builder_version=\u00a0\u00bb4.20.0&Prime; _module_preset=\u00a0\u00bbdefault\u00a0\u00bb global_colors_info=\u00a0\u00bb{}\u00a0\u00bb][\/et_pb_contact_field][et_pb_contact_field field_id=\u00a0\u00bbPhone\u00a0\u00bb field_title=\u00a0\u00bbT\u00e9l\u00e9phone *\u00a0\u00bb _builder_version=\u00a0\u00bb4.20.4&Prime; _module_preset=\u00a0\u00bbdefault\u00a0\u00bb global_colors_info=\u00a0\u00bb{}\u00a0\u00bb][\/et_pb_contact_field][et_pb_contact_field field_id=\u00a0\u00bbLocation\u00a0\u00bb field_title=\u00a0\u00bbVille *\u00a0\u00bb _builder_version=\u00a0\u00bb4.19.5&Prime; _module_preset=\u00a0\u00bbdefault\u00a0\u00bb global_colors_info=\u00a0\u00bb{}\u00a0\u00bb][\/et_pb_contact_field][et_pb_contact_field field_id=\u00a0\u00bbCountry\u00a0\u00bb field_title=\u00a0\u00bbPays *\u00a0\u00bb field_type=\u00a0\u00bbselect\u00a0\u00bb select_options=\u00a0\u00bb%91{%22value%22:%22\u00c9tats-Unis%22,%22checked%22:0,%22dragID%22:-1},{%22value%22:%22Royaume-Uni%22,%22checked%22:0,%22dragID%22:0},{%22value%22:%22Afghanistan%22,%22checked%22:0,%22dragID%22:1},{%22value%22:%22Albanie%22,%22checked%22:0,%22dragID%22:2},{%22value%22:%22Alg\u00e9rie%22,%22checked%22:0,%22dragID%22:3},{%22value%22:%22Angola%22,%22checked%22:0,%22dragID%22:4},{%22value%22:%22Antigua-et-Barbuda%22,%22checked%22:0,%22dragID%22:5},{%22value%22:%22Argentine%22,%22checked%22:0,%22dragID%22:6},{%22value%22:%22Arm\u00e9nie%22,%22checked%22:0,%22dragID%22:7},{%22value%22:%22Autriche%22,%22checked%22:0,%22dragID%22:8},{%22value%22:%22Australie%22,%22checked%22:0,%22dragID%22:190},{%22value%22:%22Azerba\u00efdjan%22,%22checked%22:0,%22dragID%22:9},{%22value%22:%22Bahamas%22,%22checked%22:0,%22dragID%22:10},{%22value%22:%22Bahre\u00efn%22,%22checked%22:0,%22dragID%22:11},{%22value%22:%22Bangladesh%22,%22checked%22:0,%22dragID%22:12},{%22value%22:%22Barbade%22,%22checked%22:0,%22dragID%22:13},{%22value%22:%22Bi\u00e9lorussie%22,%22checked%22:0,%22dragID%22:14},{%22value%22:%22Belgique%22,%22checked%22:0,%22dragID%22:15},{%22value%22:%22Belize%22,%22checked%22:0,%22dragID%22:16},{%22value%22:%22B\u00e9nin%22,%22checked%22:0,%22dragID%22:17},{%22value%22:%22Bhoutan%22,%22checked%22:0,%22dragID%22:18},{%22value%22:%22Bolivie%22,%22checked%22:0,%22dragID%22:19},{%22value%22:%22Bosnie-Herz\u00e9govine%22,%22checked%22:0,%22dragID%22:20},{%22value%22:%22Botswana%22,%22checked%22:0,%22dragID%22:21},{%22value%22:%22Br\u00e9sil%22,%22checked%22:0,%22dragID%22:22},{%22value%22:%22Brunei%22,%22checked%22:0,%22dragID%22:23},{%22value%22:%22Bulgarie%22,%22checked%22:0,%22dragID%22:24},{%22value%22:%22Burkina Faso%22,%22checked%22:0,%22dragID%22:25},{%22value%22:%22Burundi%22,%22checked%22:0,%22dragID%22:26},{%22value%22:%22Cabo Verde%22,%22checked%22:0,%22dragID%22:27},{%22value%22:%22Cambodge%22,%22checked%22:0,%22dragID%22:28},{%22value%22:%22Cameroun%22,%22checked%22:0,%22dragID%22:29},{%22value%22:%22Canada%22,%22checked%22:0,%22dragID%22:30},{%22value%22:%22R\u00e9publique centrafricaine%22,%22checked%22:0,%22dragID%22:31},{%22value%22:%22Tchad%22,%22checked%22:0,%22dragID%22:32},{%22value%22:%22Chili%22,%22checked%22:0,%22dragID%22:33},{%22value%22:%22Colombie%22,%22checked%22:0,%22dragID%22:34},{%22value%22:%22Comores%22,%22checked%22:0,%22dragID%22:35},{%22value%22:%22Costa Rica%22,%22checked%22:0,%22dragID%22:36},{%22value%22:%22Croatie%22,%22checked%22:0,%22dragID%22:37},{%22value%22:%22Cuba%22,%22checked%22:0,%22dragID%22:38},{%22value%22:%22Chypre%22,%22checked%22:0,%22dragID%22:39},{%22value%22:%22R\u00e9publique tch\u00e8que%22,%22checked%22:0,%22dragID%22:40},{%22value%22:%22RD Congo%22,%22checked%22:0,%22dragID%22:41},{%22value%22:%22Danemark%22,%22checked%22:0,%22dragID%22:42},{%22value%22:%22Djibouti%22,%22checked%22:0,%22dragID%22:43},{%22value%22:%22Dominique%22,%22checked%22:0,%22dragID%22:44},{%22value%22:%22R\u00e9publique dominicaine%22,%22checked%22:0,%22dragID%22:45},{%22value%22:%22Timor oriental%22,%22checked%22:0,%22dragID%22:46},{%22value%22:%22\u00c9quateur%22,%22checked%22:0,%22dragID%22:47},{%22value%22:%22\u00c9gypte%22,%22checked%22:0,%22dragID%22:48},{%22value%22:%22Salvador%22,%22checked%22:0,%22dragID%22:49},{%22value%22:%22Guin\u00e9e \u00e9quatoriale%22,%22checked%22:0,%22dragID%22:50},{%22value%22:%22\u00c9rythr\u00e9e%22,%22checked%22:0,%22dragID%22:51},{%22value%22:%22Estonie%22,%22checked%22:0,%22dragID%22:52},{%22value%22:%22\u00c9thiopie%22,%22checked%22:0,%22dragID%22:53},{%22value%22:%22Fidji%22,%22checked%22:0,%22dragID%22:54},{%22value%22:%22Finlande%22,%22checked%22:0,%22dragID%22:55},{%22value%22:%22France%22,%22checked%22:0,%22dragID%22:56},{%22value%22:%22Gabon%22,%22checked%22:0,%22dragID%22:57},{%22value%22:%22Gambie%22,%22checked%22:0,%22dragID%22:58},{%22value%22:%22G\u00e9orgie%22,%22checked%22:0,%22dragID%22:59},{%22value%22:%22Allemagne%22,%22checked%22:0,%22dragID%22:60},{%22value%22:%22Ghana%22,%22checked%22:0,%22dragID%22:61},{%22value%22:%22Gr\u00e8ce%22,%22checked%22:0,%22dragID%22:62},{%22value%22:%22Groenland%22,%22checked%22:0,%22dragID%22:63},{%22value%22:%22Grenade%22,%22checked%22:0,%22dragID%22:64},{%22value%22:%22Guatemala%22,%22checked%22:0,%22dragID%22:65},{%22value%22:%22Guin\u00e9e%22,%22checked%22:0,%22dragID%22:66},{%22value%22:%22Guyana%22,%22checked%22:0,%22dragID%22:67},{%22value%22:%22Ha\u00efti%22,%22checked%22:0,%22dragID%22:68},{%22value%22:%22Honduras%22,%22checked%22:0,%22dragID%22:69},{%22value%22:%22Hong Kong%22,%22checked%22:0,%22dragID%22:70},{%22value%22:%22Hongrie%22,%22checked%22:0,%22dragID%22:71},{%22value%22:%22Islande%22,%22checked%22:0,%22dragID%22:72},{%22value%22:%22Inde%22,%22checked%22:0,%22dragID%22:73},{%22value%22:%22Indon\u00e9sie%22,%22checked%22:0,%22dragID%22:74},{%22value%22:%22Iran%22,%22checked%22:0,%22dragID%22:75},{%22value%22:%22Irak%22,%22checked%22:0,%22dragID%22:76},{%22value%22:%22Irlande%22,%22checked%22:0,%22dragID%22:77},{%22value%22:%22Isra\u00ebl%22,%22checked%22:0,%22dragID%22:78},{%22value%22:%22Italie%22,%22checked%22:0,%22dragID%22:79},{%22value%22:%22C\u00f4te d&#039;Ivoire%22,%22checked%22:0,%22dragID%22:80},{%22value%22:%22Jama\u00efque%22,%22checked%22:0,%22dragID%22:81},{%22value%22:%22Japon%22,%22checked%22:0,%22dragID%22:82},{%22value%22:%22Jordanie%22,%22checked%22:0,%22dragID%22:83},{%22value%22:%22Kazakhstan%22,%22checked%22:0,%22dragID%22:84},{%22value%22:%22Kenya%22,%22checked%22:0,%22dragID%22:85},{%22value%22:%22Kiribati%22,%22checked%22:0,%22dragID%22:86},{%22value%22:%22Kosovo%22,%22checked%22:0,%22dragID%22:87},{%22value%22:%22Kowe\u00eft%22,%22checked%22:0,%22dragID%22:88},{%22value%22:%22Kirghizistan%22,%22checked%22:0,%22dragID%22:89},{%22value%22:%22Laos%22,%22checked%22:0,%22dragID%22:90},{%22value%22:%22Lettonie%22,%22checked%22:0,%22dragID%22:91},{%22value%22:%22Liban%22,%22checked%22:0,%22dragID%22:92},{%22value%22:%22Lesotho%22,%22checked%22:0,%22dragID%22:93},{%22value%22:%22Liberia%22,%22checked%22:0,%22dragID%22:94},{%22value%22:%22Libye%22,%22checked%22:0,%22dragID%22:95},{%22value%22:%22Liechtenstein%22,%22checked%22:0,%22dragID%22:96},{%22value%22:%22Lituanie%22,%22checked%22:0,%22dragID%22:97},{%22value%22:%22Luxembourg%22,%22checked%22:0,%22dragID%22:98},{%22value%22:%22Mac\u00e9doine%22,%22checked%22:0,%22dragID%22:99},{%22value%22:%22Madagascar%22,%22checked%22:0,%22dragID%22:100},{%22value%22:%22Malawi%22,%22checked%22:0,%22dragID%22:101},{%22value%22:%22Malaisie%22,%22checked%22:0,%22dragID%22:102},{%22value%22:%22Maldives%22,%22checked%22:0,%22dragID%22:103},{%22value%22:%22Mali%22,%22checked%22:0,%22dragID%22:104},{%22value%22:%22Malte%22,%22checked%22:0,%22dragID%22:105},{%22value%22:%22\u00celes Marshall%22,%22checked%22:0,%22dragID%22:106},{%22value%22:%22Mauritanie%22,%22checked%22:0,%22dragID%22:107},{%22value%22:%22Maurice%22,%22checked%22:0,%22dragID%22:108},{%22value%22:%22Mexique%22,%22checked%22:0,%22dragID%22:109},{%22value%22:%22Micron\u00e9sie%22,%22checked%22:0,%22dragID%22:110},{%22value%22:%22Moldavie%22,%22checked%22:0,%22dragID%22:111},{%22value%22:%22Monaco%22,%22checked%22:0,%22dragID%22:112},{%22value%22:%22Mongolie%22,%22checked%22:0,%22dragID%22:113},{%22value%22:%22Mont\u00e9n\u00e9gro%22,%22checked%22:0,%22dragID%22:114},{%22value%22:%22Maroc%22,%22checked%22:0,%22dragID%22:115},{%22value%22:%22Mozambique%22,%22checked%22:0,%22dragID%22:116},{%22value%22:%22Myanmar%22,%22checked%22:0,%22dragID%22:117},{%22value%22:%22Namibie%22,%22checked%22:0,%22dragID%22:118},{%22value%22:%22Nauru%22,%22checked%22:0,%22dragID%22:119},{%22value%22:%22N\u00e9pal%22,%22checked%22:0,%22dragID%22:120},{%22value%22:%22Pays-Bas%22,%22checked%22:0,%22dragID%22:121},{%22value%22:%22Nouvelle-Z\u00e9lande%22,%22checked%22:0,%22dragID%22:122},{%22value%22:%22Nicaragua%22,%22checked%22:0,%22dragID%22:123},{%22value%22:%22Niger%22,%22checked%22:0,%22dragID%22:124},{%22value%22:%22Nigeria%22,%22checked%22:0,%22dragID%22:125},{%22value%22:%22Cor\u00e9e du Nord%22,%22checked%22:0,%22dragID%22:126},{%22value%22:%22Norv\u00e8ge%22,%22checked%22:0,%22dragID%22:127},{%22value%22:%22Oman%22,%22checked%22:0,%22dragID%22:128},{%22value%22:%22Pakistan%22,%22checked%22:0,%22dragID%22:129},{%22value%22:%22Palaos%22,%22checked%22:0,%22dragID%22:130},{%22value%22:%22Palestine%22,%22checked%22:0,%22dragID%22:131},{%22value%22:%22Panama%22,%22checked%22:0,%22dragID%22:132},{%22value%22:%22Papouasie-Nouvelle-Guin\u00e9e%22,%22checked%22:0,%22dragID%22:133},{%22value%22:%22Paraguay%22,%22checked%22:0,%22dragID%22:134},{%22value%22:%22P\u00e9rou%22,%22checked%22:0,%22dragID%22:135},{%22value%22:%22Philippines%22,%22checked%22:0,%22dragID%22:136},{%22value%22:%22Pologne%22,%22checked%22:0,%22dragID%22:137},{%22value%22:%22Portugal%22,%22checked%22:0,%22dragID%22:138},{%22value%22:%22Porto Rico%22,%22checked%22:0,%22dragID%22:139},{%22value%22:%22Qatar%22,%22checked%22:0,%22dragID%22:140},{%22value%22:%22R\u00e9publique du Congo%22,%22checked%22:0,%22dragID%22:141},{%22value%22:%22Roumanie%22,%22checked%22:0,%22dragID%22:142},{%22value%22:%22Russie%22,%22checked%22:0,%22dragID%22:143},{%22value%22:%22Rwanda%22,%22checked%22:0,%22dragID%22:144},{%22value%22:%22Samoa%22,%22checked%22:0,%22dragID%22:145},{%22value%22:%22Saint-Marin%22,%22checked%22:0,%22dragID%22:146},{%22value%22:%22Sao Tom\u00e9-et-Principe%22,%22checked%22:0,%22dragID%22:147},{%22value%22:%22Arabie saoudite%22,%22checked%22:0,%22dragID%22:148},{%22value%22:%22S\u00e9n\u00e9gal%22,%22checked%22:0,%22dragID%22:149},{%22value%22:%22Serbie%22,%22checked%22:0,%22dragID%22:150},{%22value%22:%22Sierra Leone%22,%22checked%22:0,%22dragID%22:151},{%22value%22:%22Singapour%22,%22checked%22:0,%22dragID%22:152},{%22value%22:%22Slovaquie%22,%22checked%22:0,%22dragID%22:153},{%22value%22:%22Slov\u00e9nie%22,%22checked%22:0,%22dragID%22:154},{%22value%22:%22Somalie%22,%22checked%22:0,%22dragID%22:155},{%22value%22:%22Afrique du Sud%22,%22checked%22:0,%22dragID%22:156},{%22value%22:%22Cor\u00e9e du Sud%22,%22checked%22:0,%22dragID%22:157},{%22value%22:%22Soudan du Sud%22,%22checked%22:0,%22dragID%22:158},{%22value%22:%22Espagne%22,%22checked%22:0,%22dragID%22:159},{%22value%22:%22Sri Lanka%22,%22checked%22:0,%22dragID%22:160},{%22value%22:%22Soudan%22,%22checked%22:0,%22dragID%22:161},{%22value%22:%22Eswatini%22,%22checked%22:0,%22dragID%22:162},{%22value%22:%22Su\u00e8de%22,%22checked%22:0,%22dragID%22:163},{%22value%22:%22Suisse%22,%22checked%22:0,%22dragID%22:164},{%22value%22:%22Syrie%22,%22checked%22:0,%22dragID%22:165},{%22value%22:%22Ta\u00efwan%22,%22checked%22:0,%22dragID%22:166},{%22value%22:%22Tadjikistan%22,%22checked%22:0,%22dragID%22:167},{%22value%22:%22Tanzanie%22,%22checked%22:0,%22dragID%22:168},{%22value%22:%22Tha\u00eflande%22,%22checked%22:0,%22dragID%22:169},{%22value%22:%22Togo%22,%22checked%22:0,%22dragID%22:170},{%22value%22:%22Tonga%22,%22checked%22:0,%22dragID%22:171},{%22value%22:%22Transnistrie%22,%22checked%22:0,%22dragID%22:172},{%22value%22:%22Tunisie%22,%22checked%22:0,%22dragID%22:173},{%22value%22:%22Turquie%22,%22checked%22:0,%22dragID%22:174},{%22value%22:%22Turkm\u00e9nistan%22,%22checked%22:0,%22dragID%22:175},{%22value%22:%22Tuvalu%22,%22checked%22:0,%22dragID%22:176},{%22value%22:%22Ouganda%22,%22checked%22:0,%22dragID%22:177},{%22value%22:%22Ukraine%22,%22checked%22:0,%22dragID%22:178},{%22value%22:%22\u00c9mirats arabes unis%22,%22checked%22:0,%22dragID%22:179},{%22value%22:%22Uruguay%22,%22checked%22:0,%22dragID%22:180},{%22value%22:%22Ouzb\u00e9kistan%22,%22checked%22:0,%22dragID%22:181},{%22value%22:%22Vanuatu%22,%22checked%22:0,%22dragID%22:182},{%22value%22:%22Vatican%22,%22checked%22:0,%22dragID%22:183},{%22value%22:%22Venezuela%22,%22checked%22:0,%22dragID%22:184},{%22value%22:%22Vietnam%22,%22checked%22:0,%22dragID%22:185},{%22value%22:%22Sahara occidental%22,%22checked%22:0,%22dragID%22:186},{%22value%22:%22Y\u00e9men%22,%22checked%22:0,%22dragID%22:187},{%22value%22:%22Zambie%22,%22checked%22:0,%22dragID%22:188},{%22value%22:%22Zimbabwe%22,%22checked%22:0,%22dragID%22:189}%93&Prime; _builder_version=\u00a0\u00bb4.27.0&Prime; _module_preset=\u00a0\u00bbdefault\u00a0\u00bb form_field_line_height=\u00a0\u00bb1.4em\u00a0\u00bb global_colors_info=\u00a0\u00bb{}\u00a0\u00bb][\/et_pb_contact_field][et_pb_contact_field field_id=\u00a0\u00bbSource\u00a0\u00bb field_title=\u00a0\u00bbComment nous avez-vous connus ? *\u00a0\u00bb field_type=\u00a0\u00bbcheckbox\u00a0\u00bb checkbox_options=\u00a0\u00bb%91{%22value%22:%22Recherche Internet%22,%22checked%22:0,%22dragID%22:-1},{%22value%22:%22Newsletter%22,%22checked%22:0,%22dragID%22:0},{%22value%22:%22Coll\u00e8gue%22,%22checked%22:0,%22dragID%22:1},{%22value%22:%22Article scientifique%22,%22checked%22:0,%22dragID%22:2},{%22value%22:%22Autre%22,%22checked%22:0,%22dragID%22:3}%93&Prime; _builder_version=\u00a0\u00bb4.20.4&Prime; _module_preset=\u00a0\u00bbdefault\u00a0\u00bb form_field_background_color=\u00a0\u00bb#FFFFFF\u00a0\u00bb form_field_text_color=\u00a0\u00bb#6B6B6B\u00a0\u00bb form_field_focus_background_color=\u00a0\u00bb#7CDA24&Prime; form_field_focus_text_color=\u00a0\u00bb#00448B\u00a0\u00bb form_field_font=\u00a0\u00bb|600|||||||\u00a0\u00bb form_field_font_size=\u00a0\u00bb14px\u00a0\u00bb max_width=\u00a0\u00bb250px\u00a0\u00bb border_width_all=\u00a0\u00bb2px\u00a0\u00bb border_color_all=\u00a0\u00bb#6B6B6B\u00a0\u00bb global_colors_info=\u00a0\u00bb{}\u00a0\u00bb][\/et_pb_contact_field][et_pb_contact_field field_id=\u00a0\u00bbProducts\u00a0\u00bb field_title=\u00a0\u00bbQuels produits vous int\u00e9ressent ? *\u00a0\u00bb field_type=\u00a0\u00bbcheckbox\u00a0\u00bb checkbox_options=\u00a0\u00bb%91{%22value%22:%22PhotoRedOx Box%22,%22checked%22:0,%22dragID%22:-1},{%22value%22:%22PhotoRedOx Box TC%22,%22checked%22:0,%22dragID%22:0},{%22value%22:%22PhotoRedOx Box Duo%22,%22checked%22:0,%22dragID%22:1},{%22value%22:%22Lucent360%22,%22checked%22:0,%22dragID%22:2},{%22value%22:%22Sources lumineuses%22,%22checked%22:0,%22dragID%22:3},{%22value%22:%22Lampes UV%22,%22checked%22:0,%22dragID%22:4},{%22value%22:%22Flacons en quartz%22,%22checked%22:0,%22dragID%22:5},{%22value%22:%22Protection contre la lumi\u00e8re%22,%22checked%22:0,%22dragID%22:6},{%22value%22:%22Packs de d\u00e9marrage%22,%22checked%22:0,%22dragID%22:7},{%22value%22:%22Autre chose%22,%22checked%22:0,%22dragID%22:8}%93&Prime; _builder_version=\u00a0\u00bb4.20.4&Prime; _module_preset=\u00a0\u00bbdefault\u00a0\u00bb form_field_font=\u00a0\u00bb|600|||||||\u00a0\u00bb form_field_font_size=\u00a0\u00bb14px\u00a0\u00bb width=\u00a0\u00bb100%\u00a0\u00bb global_colors_info=\u00a0\u00bb{}\u00a0\u00bb][\/et_pb_contact_field][et_pb_contact_field field_id=\u00a0\u00bbQuestions\u00a0\u00bb field_title=\u00a0\u00bb\u00cates-vous \u00e9galement int\u00e9ress\u00e9 par d\u2019autres produits ou services ? Veuillez ajouter des d\u00e9tails ou des questions suppl\u00e9mentaires ici. \u00a0\u00bb field_type=\u00a0\u00bbtext\u00a0\u00bb required_mark=\u00a0\u00bboff\u00a0\u00bb _builder_version=\u00a0\u00bb4.20.4&Prime; _module_preset=\u00a0\u00bbdefault\u00a0\u00bb global_colors_info=\u00a0\u00bb{}\u00a0\u00bb][\/et_pb_contact_field][\/et_pb_contact_form][et_pb_text _builder_version=\u00a0\u00bb4.27.6&Prime; _module_preset=\u00a0\u00bbdefault\u00a0\u00bb global_colors_info=\u00a0\u00bb{}\u00a0\u00bb]<\/p>\n<h2 style=\"text-align: center;\">Plus de 500 publications depuis 2018<\/h2>\n<p>quelques exemples.<\/p>\n<p>(1) Seefeldt, P.; Villinger, A.; Brasholz, M. Photoredox-Catalyzed Carbon Radical Generation from \u03b1-Keto- N , O -Acetals\u202f: Synthesis of Functionalized Azepino [ 1 , 2- a ] Indoles and Azepino [ 1 , 2- a ] Furo [ 3 , 2- b ] Indoles. <em>Adv. Synth. Catal.<\/em> <strong>2024<\/strong>, <em>366<\/em> (1), 24\u201330.<\/p>\n<p>(2) Adri\u00e1n Luguera Ruiz; Mariani, E.; Stefano Protti; Fagnoni, M. Photoredox Catalyzed Release of Carbon-Based Radicals from 2- Substituted-1,3-Imidazolidines. <em>Org. Chem. Front.<\/em> <strong>2024<\/strong>. https:\/\/doi.org\/10.1039\/D3QO01856C.<\/p>\n<p>(3) Fu-Peng Wu, Chetan C. Chintawar, Remy Lalisse, Poulami Mukherjee, Subhabrata Dutta, Jasper Tyler, Constantin G. Daniliuc, O. G. &#038; F. G. Ring Expansion of Indene by Photoredox- Enabled Functionalized Carbon-Atom Insertion. <em>Nat. Catal.<\/em> <strong>2024<\/strong>.<\/p>\n<p>(4) Dutta, S.; Lee, D.; Ozols, K.; Daniliuc, C. G.; Shintani, R.; Glorius, F. Photoredox-Enabled Dearomative [2\u03c0 + 2\u03c3] Cycloaddition of Phenols. <em>J. Am. Chem. Soc.<\/em> <strong>2024<\/strong>, 1\u2013116. https:\/\/doi.org\/10.1021\/jacs.3c12894.<\/p>\n<p>(5) Revie, R. I.; Whitaker, B. J.; Paul, B.; Smith, R. C.; Anderson, E. A. Synthesis of Heterocycle-Substituted Bicyclo[3.1.1]Heptanes and Aza-Bicyclo[3.1.1]Heptanes via Photocatalytic Minisci Reaction. <em>Org. Lett.<\/em> <strong>2024<\/strong>, 10\u201313. https:\/\/doi.org\/10.1021\/acs.orglett.3c03684.<\/p>\n<p>(6) Yadav, A. K.; Ariff, P. N. A. M.; Kawai, K.; Ochiai, S.; Narra, S. R.; Shibata, N. Cross Dehydrogenative Coupling of SF4-Alkyne with Tetrahydroisoquinolines. <em>Org. Lett.<\/em> <strong>2024<\/strong>.<\/p>\n<p>(7) Kim, S. F.; Schwarz, H.; Jurczyk, J.; Nebgen, B. R.; Hendricks, H.; Park, H.; Radosevich, A.; Zuerch, M. W.; Harper, K.; Lux, M. C.; Yeung, C. S.; Sarpong, R. Mechanistic Investigation, Wavelength-Dependent Reactivity, and Expanded Reactivity of N-Aryl Azacycle Photomediate Ring Contractions. <em>J. Am. Chem. Soc<\/em> <strong>2024<\/strong>. https:\/\/doi.org\/10.1021\/jacs.3c13982.<\/p>\n<p>(8) Subhabrata Dutta, Yi-Lin Lu, Johannes E. Erchinger, Huiling Shao, Emanuel Studer, Felix Sch\u00e4fer, Huamin Wang, Debanjan Rana, Constantin G. Daniliuc, K. N. Houk,* and Frank Glorius Shao, Emanuel Studer, Felix Sch\u00e4fer, Huamin Wang, Debanjan Rana, Constantin, and F. G. Double Strain-Release[2\u03c0+2\u03c3]-Photocycloaddition. <em>J. Am. Chem. Soc<\/em> <strong>2024<\/strong>, No. 1, 1\u20135.<\/p>\n<p>(9) Dam, D.; Lagerweij, N. R.; Janmaat, K. M.; Kok, K.; Bouwman, E.; Cod, J. D. C. Organic Dye-Sensitized Nitrene Generation: Intermolecular Aziridination of Unactivated Alkenes. <em>J. Am. Chem. Soc<\/em> <strong>2024<\/strong>, 1\u201387. https:\/\/doi.org\/10.1021\/acs.joc.3c02709.<\/p>\n<p>(10) Igor A. Lavrinchenko , Egor A. Nikiforov , Timofey D. Moseev , Mikhail V. Varaksin \u2217 , Anton N. Tsmokalyuk , Thomas V. Nechaev , Valery N. Charushin, O. N. Synthesis, Photophysical, and AIE Properties of 2H-Imidazole-Derived Push-Pull Fluorophores. <em>Synthesis (Stuttg).<\/em> <strong>2024<\/strong>.<\/p>\n<p>(11) Hervieu, C.; Kirillova, M. S.; Hu, Y.; Cuesta-galisteo, S.; Merino, E.; Nevado, C. Chiral Arylsulfinylamides as Reagents for Visible Light-Mediated Asymmetric Alkene Aminoarylations. <em>Nat. Chem.<\/em> <strong>2024<\/strong>, 1\u201318. https:\/\/doi.org\/10.1038\/s41557-023-01414-8.<\/p>\n<p>(12) Gesmundo, N. J.; Rago, A. J.; Young, J. M.; Keess, S.; Wang, Y. At the Speed of Light: The Systematic Implementation of Photoredox Cross-Coupling Reactions for Medicinal Chemistry Research. <em>J. Org. Chem.<\/em> <strong>2024<\/strong>, 1\u201328. https:\/\/doi.org\/10.1021\/acs.joc.3c02351.<\/p>\n<p>(13) Seefeldt, P.; Edelmann, L.; Prudlik, A.; Villinger, A.; Francke, R.; Brasholz, M. Photoinduced Tandem C-O Bond Reduction \/ Ketyl Radical Addition Reactions of \u03b1 -Keto- N , O -Acetals Enabled by Proton-Coupled Electron Transfer. <em>ChemPhotoChem<\/em> <strong>2024<\/strong>.<\/p>\n<p>(14) Han, G.; You, J.; Choi, J.; Joo, E. N -Iminopyridinium Compounds in Giese Reaction\u202f: Photoinduced Homolytic N-N and C-C Bond Cleavage for Cyanoalkyl Radical Generation. <em>Org. Lett.<\/em> <strong>2024<\/strong>, 1\u201399.<\/p>\n<p>(15) Bonfils, P. De; Nun, P.; Coeffard, V. Unsymmetrical Anthracene Platforms as Singlet Oxygen Batteries\u202f: Effects of Substituents on Photooxygenation and Endoperoxide Thermolysis. <em>European J. Org. Chem.<\/em> <strong>2024<\/strong>, <em>202400099<\/em> (1), 4\u20135. https:\/\/doi.org\/10.1002\/ejoc.200490000.<\/p>\n<p>(16) Tagami, T.; Kawamura, S.; Sodeoka, M. Aerobic Photoredox Catalyzed Oxamate Ester Synthesis from Bromodifluoroacetate Esters. <em>European J. Org. Chem.<\/em> <strong>2024<\/strong>.<\/p>\n<p>(17) Laskar, R.; Dutta, S.; Spies, J. C.; Mukherjee, P.; Renter\u00eda-g\u00f3mez, \u00c1. \u0393\u2011Amino Alcohols via Energy Transfer Enabled Brook Rearrangement. <em>J. Am. Chem. Soc<\/em> <strong>2024<\/strong>.<\/p>\n<p>(18) Magkoev, T. T.; Demidov, O. P.; Abaev, V. T.; Uchuskin, M. G.; Chalikidi, P. N. Unveiling Orthogonal Reactivity of Substituted 2\u2011(2- Azidostyryl)Furans: Thermolysis and Photolysis versus Catalysis. <em>J. Org. Chem.<\/em> <strong>2024<\/strong>, 1\u201368. https:\/\/doi.org\/10.1021\/acs.joc.4c00355.<\/p>\n<p>(19) Ramos, A. L.; Goedken, E. R.; Frank, K. E.; Argiriadi, M. A.; Bazzaz, S.; Bian, Z.; Brown, J. T. C.; Centrella, P. A.; Chen, H.; Disch, J. S.; Donner, P. L.; Duignan, D. B.; Gikunju, D.; Greszler, S. N.; Gui, M.; Habeshian, S.; Hartl, H. E.; Hein, C. D.; Hutchins, C. W.; Jetson, R.; Keefe, A. D.; Khan, H.; Li, H.; Olszewski, A.; Cardona, B. J. O.; Osuma, A.; Panchal, S. C.; Phelan, R.; Qiu, W.; Shotwell, J. B.; Shrestha, A.; Srikumaran, M.; Su, Z.; Sun, C.; Upadhyay, A. K.; Wood, M. D.; Wu, H.; Zhang, R.; Zhang, Y.; Zhao, G.; Zhu, H.; Webster, M. P. Discovery of Small Molecule Interleukin 17A Inhibitors with Novel Binding Mode and Stoichiometry: Optimization of DNA-Encoded Chemical Library Hits to In Vivo Active Compounds. <em>J. Med. Chem.<\/em> <strong>2024<\/strong>.  https:\/\/doi.org\/10.1021\/acs.jmedchem.3c02397.<\/p>\n<p>(20) Chintawar, C. C.; Laskar, R.; Rana, D.; Wyngaerden, N. Van; Dutta, S.; Daniliuc, C. G.; Glorius, F. Photoredox-Catalyzed Amidyl Radical Insertion to Bicyclo[1.1.0]. <em>ChemRxiv. Prepr.<\/em> <strong>2024<\/strong>.<\/p>\n<p>(21) Krax, R.; Menneking, K.; Sajapin, J.; Hellwig, M. Identification of \u03b2-Aspartic Semialdehyde and Homocysteine as Major Reaction Products of Riboflavin-Sensitized Photooxidation of Peptide-Bound Methionine. <em>Eur. Food Res. Technol.<\/em> <strong>2024<\/strong>. https:\/\/doi.org\/10.1007\/s00217-024-04540-w.<\/p>\n<p>(22) Jonathan Da Luz , Michaela \u010cierna , Bradley D. Cooper , Thomas D. Harris , Ethan R. X. Lim , Jonathan R. Carney, M. J. J. Denitrative Sulfonylation of Nitroarenes with Sodium Sulfinates. <em>Synthesis (Stuttg).<\/em> <strong>2024<\/strong>.<\/p>\n<p>(23) Lilian Geniller, Marc Taillefer, Eric Clot, Florian Jaroschik, and A. P. Photocatalyzed Formation of Gem\u2010difluoroalkenes Using Oxime Esters. <em>Adv. Synth. Catal.<\/em> <strong>2024<\/strong>, 1\u201323.<\/p>\n<p>(24) Karlsson, S.; Leonori, D.; Plesniak, M. P. Mild Strategy for the Preparation of Alkyl Sulfonyl Fluorides from Alkyl Bromides and Alcohols Using Photoredox Catalysis and Flow Chemistry. <em>Org. Lett.<\/em> <strong>2024<\/strong>, <em>2<\/em> (1), 1\u20135. https:\/\/doi.org\/10.1021\/acs.orglett.4c01216.<\/p>\n<p>(25) Ortalli, S.; Ford, J.; Trabanco, A. A.; Tredwell, M.; Gouverneur, V. Photoredox Nucleophilic ( Radio ) Fluorination of Alkoxyamines. <em>J. Am. Chem. Soc<\/em> <strong>2024<\/strong>, 0\u20135. https:\/\/doi.org\/10.1021\/jacs.4c02474.<\/p>\n<p>(26) Mocny, P.; Lin, T.; Parekh, R.; Zhao, Y.; Czarnota, M.; Urban, M.; Majidi, C.; Matyjaszewski, K. Selective and Controlled Grafting from PVDF-Based Materials by Oxygen-Tolerant Green-Light-Mediated ATRP \u0301. <em>Appl. Mater. Interfaces<\/em> <strong>2024<\/strong>, 1\u201334. https:\/\/doi.org\/10.1021\/acsami.4c03369.<\/p>\n<p>(27) Hu, T.; Fagu\u00e9, V.; Bouyssi, D.; Monteiro, N.; Amgoune, A. Hydride-Free Reduction of Propargyl Electrophiles: A Nickel-Catalyzed Photoredox Strategy for Allene Synthesis. <em>Green Chem.<\/em> <strong>2024<\/strong>. https:\/\/doi.org\/10.1039\/d4gc00984c.<\/p>\n<p>(28) Alcaraz, M.; Lyonnais, S.; Ghosh, C.; Aguilera-correa, J. J.; Richeter, S.; Ulrich, S.; Kremer, L.; Alcaraz, M.; Lyonnais, S.; Ghosh, C.; Aguilera-correa, J. J.; Richeter, S.; Ulrich, S.; Kremer, L. Evaluation and Activity of New Porphyrin-Peptide Cage-Type Conjugates for the Photoinactivation of Mycobacterium Abscessus. <em>Microbiol. Spectr.<\/em> <strong>2024<\/strong>, No. April. <\/p>\n<p>(29) Hu, X.; Yin, R.; Jeong, J.; Matyjaszewski, K.; Information, S.; Hu, X.; Yin, R.; Jeong, J.; Matyjaszewski, K. Robust Miniemulsion PhotoATRP Driven by Red and Near-Infrared Light. <em>J. Am. Chem. Soc<\/em> <strong>2024<\/strong>. https:\/\/doi.org\/10.1021\/jacs.4c02553.<\/p>\n<p>(30) El-Arid, S.; Lenihan, J.; Jacobsen, A.; Beeler, A.; Grinstaff, M. Accessing Cyclobutane Polymers: Overcoming Synthetic Challenges via Efficient Continuous Flow [2+2] Photopolymerization. <em>ACS MacroLetters<\/em> <strong>2024<\/strong>. https:\/\/doi.org\/10.1021\/acsmacrolett.4c00083.<\/p>\n<p>(31) Kechiche, A.; Shaymaa Al Shehimy, L. K.; Monnereau, C.; Christophe Bucher, S. P.; Alla Bessmertnykh-Lemeune, Y. R.; Nasri, A. V. C. and H. Phosphonate-Substituted Porphyrins as Efficient, Cost-Effective and Reusable Photocatalysts. <em>Dalt. Trans.<\/em> <strong>2024<\/strong>.<\/p>\n<p>(32) Tambe, S. D.; Hwang, H. S.; Park, E.; Cho, E. J. Dual Photoredox and Nickel Catalysis in Regioselective Diacylation\u202f: Exploring the Versatility of Nickel Oxidation States in Allene Activation. <em>Org. Lett.<\/em> <strong>2024<\/strong>.<\/p>\n<p>(33) Yoshida, Y.; Takeuchi, H.; Arichi, N.; Oishi, S.; Ohno, H.; Inuki, S. Approach to Spirocyclohexadienes via Visible Light-Mediated Ipso -Cyclization of Amino Acid Derivatives with N &#8211; ( 2-Phenyl ) Benzoyl Groups. <em>Asian J. Chem.<\/em> <strong>2024<\/strong>.<\/p>\n<p>(34) Frances R. Smith, Declan Meehan, Rhys C. Griffiths, Harriet J. Knowles, Peiyu Zhang, Huw E. L. Williams, Andrew J. Wilson, and N. J. M. Peptide Macrocyclisation via Intramolecular Interception of Visible-Light-Mediated Desulfurisation. <em>Chem. Sci.<\/em> <strong>2024<\/strong>, <em>2<\/em> (100 mL), 2\u20136. https:\/\/doi.org\/10.1038\/scientificamerican10271883-6511csupp.<\/p>\n<p>(35) Lasky, M. R.; Liu, E.; Remy, M. S.; Sanford, M. S. Visible-Light Photocatalytic C \u2212 H Amination of Arenes Utilizing Acridine \u2212 Lewis Acid Complexes. <em>J. Am. Chem. Soc<\/em> <strong>2024<\/strong>. https:\/\/doi.org\/10.1021\/cm504475k.<\/p>\n<p>(36) Tyler, J. L.; Sch\u00e4fer, F.; Shao, H.; Stein, C.; Wong, A.; Daniliuc, C. G.; Houk, K. N.; Glorius, F. Bicyclo[1.1.0]Butyl Radical Cations: Synthesis and Application to [2\u03c0+2\u03c3] Cycloaddition Reactions. <em>J. Am. Chem. Soc.<\/em> <strong>2024<\/strong>.<\/p>\n<p>(37) Guselnikova, O.; Trelin, A.; Kang, Y.; Postnikov, P.; Kobashi, M.; Suzuki, A.; Shrestha, L. K.; Henzie, J.; Yamauchi, Y. Pretreatment-Free SERS Sensing of Microplastics Using a Self-Attention-Based Neural Network on Hierarchically Porous Ag Foams. <em>Nat. Commun.<\/em> <strong>2024<\/strong>, <em>15<\/em>, 4351. https:\/\/doi.org\/10.1038\/s41467-024-48148-w.<\/p>\n<p>(38) Hynek, J.; Payne, D. T.; Shrestha, L. K.; Chahal, M. K.; Ma, R.; Dong, J.; Ariga, K.; Yamauchi, Y.; Hill, J. P. Mild Selective Photochemical Oxidation of an Organic Sulfide Using OxP-Polyimide Porous Polymers as Singlet Oxygen Generators. <em>Sci. Technol. Adv. Mater.<\/em> <strong>2024<\/strong>, <em>25<\/em> (1). https:\/\/doi.org\/10.1080\/14686996.2024.2322458.<\/p>\n<p>(39) Nugent, J.; L\u00f3pez-franc\u00e9s, A.; Sterling, A. J.; Yi, M.; Frank, N.; James, J.; Anderson, E. A. \u03b1-Amino Bicycloalkylation through Organophotoredox Catalysis. <em>Chem. Sci.<\/em> <strong>2024<\/strong>. https:\/\/doi.org\/10.1039\/D4SC01368A.<\/p>\n<p>(40) Photoreactor, Si. of E. into Z. U. a R. Mayuko Suga, Saki Fukushima, Kosho Makino, Kayo Nakamura, Hidetsugu Tabata, Tetsuta Oshitari, Hideaki Natsugari, Noritaka Kuroda, Kunio Kanemaru, Yuji Oda, and Hideyo Takahashi *. <em>J. Org. Chem.<\/em> <strong>2024<\/strong>, <em>11<\/em> (1), 1\u20135.  https:\/\/doi.org\/10.1021\/acs.joc.4c00721.<\/p>\n<p>(41) Galibert-guijarro, A.; Tronc, J.; Mouysset, D.; Siri, D.; Bertrand, M. P.; Feray, L. Investigation of UV Light-Promoted Synthesis of a -Sulfonyl Amides from N- Sulfonyl Ynamides . <em>J. Org. Chem.<\/em> <strong>2024<\/strong>, 1\u2013166.<\/p>\n<p>(42) de Blois, C.; Engel, M.; Rejou, M. A.; Molcrette, B.; Favier, A.; Montel, F. Optical Single Molecule Characterisation of Natural and Synthetic Polymers through Nanopores. <em>Nanoscale<\/em> <strong>2024<\/strong>, <em>16<\/em> (1), 138\u2013151. https:\/\/doi.org\/10.1039\/d3nr04915a.<\/p>\n<p>(43) Pijper, B.; Saavedra, L. M.; Lanzi, M.; Alonso, M.; Fontana, A.; Serrano, M.; G\u00f3mez, J. E.; Kleij, A. W.; Alc\u00e1zar, J.; Ca\u00f1ellas, S. Addressing Reproducibility Challenges in High-Throughput Photochemistry. <em>JACS Au<\/em> <strong>2024<\/strong>. https:\/\/doi.org\/10.1021\/jacsau.4c00312.<\/p>\n<p>(44) Morad, V.; Stelmakh, A.; Svyrydenko, M.; Feld, L. G.; Boehme, S. C.; Aebli, M.; Affolter, J.; Kaul, C. J.; Schrenker, N. J.; Bals, S.; Sahin, Y.; Dirin, D. N.; Cherniukh, I.; Raino, G.; Baumketner, A.; Kovalenko, M. V. Designer Phospholipid Capping Ligands for Soft Metal Halide Nanocrystals. <em>Nature<\/em> <strong>2024<\/strong>, <em>626<\/em> (7999), 542\u2013548. https:\/\/doi.org\/10.1038\/s41586-023-06932-6.<\/p>\n<p>(45) Angeltveit, C. F.; Kommedal, E. G.; Stepnov, A. A.; Eijsink, V. G. H.; Horn, S. J. Light Exposure of Lignin Affects the Saccharification Efficiency of LPMO- Containing Cellulolytic Enzyme Cocktails. <em>ACS Sustain. Chem. Eng.<\/em> <strong>2024<\/strong>, 1\u20136. https:\/\/doi.org\/10.1021\/acssuschemeng.4c02042.<\/p>\n<p>(46) Reischauer, S.; Smoljan, C. S.; Rabeah, J.; Xie, H.; Formalik, F.; Chen, Z.; Vornholt, S. M.; Sha, F.; Chapman, K. W.; Snurr, R. Q.; Notestein, J. M.; Farha, O. K. A Titanium-Based Metal\u2212Organic Framework For Tandem Metallaphotocatalysis. <em>Appl. Mater. Interfaces<\/em> <strong>2024<\/strong>.<\/p>\n<p>(47) Andrews, J. A.; Woodger, R. G.; Palmer, C. F.; Poole, D. L.; Willis, M. C. Exploiting Amine-Sulfinylamine Exchange for Photo-Decarboxylative Sulfinamidation. <em>Angew. Chem. Int. Ed.<\/em> <strong>2024<\/strong>.<\/p>\n<p>(48) Yusuke Miyamoto, Sho Murakami, Yuto Sumida, Go Hirai, H. O. Radical C-Glycosylation Using Photoexcitable Unprotected Glycosyl Borate. <em>Chem. A Eur. J.<\/em> <strong>2024<\/strong>, 1\u2013134.<\/p>\n<p>(49) Cahard, D.; Marie, N.; Ma, J.-A.; Tognetti, V. Photocatalyzed Cascade Hydrogen Atom Transfers for Assembly of Multi\u2010substituted \u0391\u2010SCF3 and \u0391\u2010SCF2H Cyclopentanones. <em>Angew. Chemie Int. Ed.<\/em> <strong>2024<\/strong>. https:\/\/doi.org\/10.1002\/anie.202407689.<\/p>\n<p>(50) Ruiz, A. L.; Benazzi, V.; Tucci, F.; Rizzo, F.; Adrian Luguera Ruiz, Valentina Benazzi, Federico Tucci, Francesca Rizzo, Daniele Merli, Stefano Protti, and M. F. Organophotocatalyzed C-Si Bond Fragmentation Using Silyl Ethers as Radical Precursors. <em>Adv. Synth. Catal.<\/em> <strong>2024<\/strong>.<\/p>\n<p>(51) Venditto, N. J.; Boerth, J. A. Deoxy-Arylation of Amides via a Tandem Hydrosilylation\/Radical- Radical Coupling Sequence. <em>Org. Lett.<\/em> <strong>2024<\/strong>, <em>26<\/em> (17), 3617\u20133621. https:\/\/doi.org\/10.1021\/acs.orglett.4c01121.<\/p>\n<p>(52) Capucciati, A.; Foli, V.; Lioniello, P.; Alfieri, M. L.; Cassera, E.; Merli, D.; Manini, P.; Ravelli, D. Exploring the Reactivity of Melanins as Photocatalysts for Reductive Dehalogenations. <em>European J. Org. Chem.<\/em> <strong>2024<\/strong>, <em>27<\/em> (20), 1\u20137. https:\/\/doi.org\/10.1002\/ejoc.202400191.<\/p>\n<p>(53) Chen, X.; Li, H.; Kramer, S. Photoinduced Copper-Catalyzed Enantioselective Allylic C ( Sp 3 )\u2013 H Oxidation of Acyclic 1-Aryl-2-Alkyl Alkenes as Limiting Substrates. <em>Angew. Chem. Int. Ed.<\/em> <strong>2024<\/strong>, 1\u2013102.<\/p>\n<p>(54) Li, M.; Yuan, Y.; Harrison, W.; Zhang, Z.; Zhao, H. Asymmetric Photoenzymatic Incorporation of Fluorinated Motifs into Olefins. <em>Science (80-. ).<\/em> <strong>2024<\/strong>, <em>385<\/em> (6707), 416\u2013421. https:\/\/doi.org\/10.1126\/science.adk8464.<\/p>\n<p>(55) Moriyama, T.; Yoritate, M.; Kato, N.; Saika, A.; Kusuhara, W.; Ono, S.; Nagatake, T.; Koshino, H.; Kiya, N.; Moritsuka, N.; Tanabe, R.; Hidaka, Y.; Usui, K.; Chiba, S.; Kudo, N.; Nakahashi, R.; Igawa, K.; Matoba, H.; Tomooka, K.; Ishikawa, E.; Takahashi, S.; Kunisawa, J.; Yamasaki, S.; Hirai, G. Linkage-Editing Pseudo-Glycans: A Reductive \u03b1-Fluorovinyl-C-Glycosylation Strategy to Create Glycan Analogs with Altered Biological Activities. <em>J. Am. Chem. Soc.<\/em> <strong>2024<\/strong>, <em>146<\/em> (3), 2237\u20132247. https:\/\/doi.org\/10.1021\/jacs.3c12581.<\/p>\n<p>(56) Jhun, B. H.; Jang, J.; Lee, S.; Cho, E. J.; You, Y. Efficient Photoredox Catalysis in C\u2013C Cross-Coupling Reactions by Two-Coordinated Au(I) Complex. <em>Nat. Commun.<\/em> <strong>2024<\/strong>, <em>15<\/em> (1), 1\u201312. https:\/\/doi.org\/10.1038\/s41467-024-50979-6.<\/p>\n<p>(57) Harfouche, N.; Marie, P.; Dragoe, D.; Le, H.; Th\u00e9bault, P.; Bilot, C.; Fouchet, A.; Rouden, J.; Baudoux, J.; Lepoittevin, B. Antibacterial Zirconia Surfaces from Organocatalyzed Atom-Transfer Radical Polymerization. <em>Materials (Basel).<\/em> <strong>2024<\/strong>, <em>17<\/em> (8). https:\/\/doi.org\/10.3390\/ma17081775.<\/p>\n<p>(58) Moritsuka, N.; Kiya, N.; Moriyama, T.; Koshino, H.; Yoritate, M.; Matoba, H.; Hirai, G. Linkage-Editing of Melibiosamine: Synthesis and Biological Evaluation of CH 2 &#8211; and CHF-Linked Analogs. <em>J. Org. Chem.<\/em> <strong>2024<\/strong>. https:\/\/doi.org\/10.1021\/acs.joc.4c01143.<\/p>\n<p>(59) Noyuri Kudo\u2021 , Suzuka Chiba\u2021 , Shunsuke Ono , Masataka Nagatoishi , Makoto Yoritate , Satoru Karasawa , Kazuteru Usui\u2217, G. H. Stereoselective Synthesis of C-Aryl-\u03b1-Glycosides by Reductive C(Sp2)-C(Sp3) Cross-Coupling Reaction. <em>Synlett<\/em> <strong>2024<\/strong>.<\/p>\n<p>(60) Hosford, B. M.; Ramos, W.; Lamb, J. R. Combining Photocontrolled-Cationic and Anionic-Group-Transfer Polymerizations Using a Universal Mediator: Enabling Access to Two- and Three-Mechanism Block Copolymers. <em>Chem. Sci.<\/em> <strong>2024<\/strong>. https:\/\/doi.org\/10.1039\/d4sc02511c.<\/p>\n<p>(61) Wu, F.; Tyler, J. L.; Daniliuc, C. G.; Glorius, F. Atomic Carbon Equivalent\u202f: Design and Application to Diversity- Generating Skeletal Editing from Indoles to 3-Functionalized Quinolines. <em>ACS Catal.<\/em> <strong>2024<\/strong>, 1\u2013189.<\/p>\n<p>(62) Emily R. Wearing, Yu-Cheng Yeh, Gianmarco G. Terrones, Seren G. Parikh, Ilia Kevlishvili, Heather J. Kulik, and C. S. S. Visible Light\u2013Mediated Aza Patern\u00f2\u2013B\u00fcchi Reaction of Acyclic Oximes and Alkenes to Azetidines Emily. <em>Science<\/em> <strong>2024<\/strong>, <em>384<\/em>. https:\/\/doi.org\/10.1126\/science.adn6384.<\/p>\n<p>(63) Boudry, E.; Bourdreux, F.; Marrot, J.; Moreau, X.; Ghiazza, C. Dearomatization of Pyridines: Photochemical Skeletal Enlargement for the Synthesis of 1,2-Diazepines. <em>J. Am. Chem. Soc.<\/em> <strong>2024<\/strong>, <em>146<\/em> (4), 2845\u20132854. https:\/\/doi.org\/10.1021\/jacs.3c14467.<\/p>\n<p>(64) Zhang, T.; Rabeah, J.; Das, S. Red-Light-Mediated Copper-Catalyzed Photoredox Catalysis Promotes Regioselectivity Switch in the Difunctionalization of Alkenes. <em>Nat. Commun.<\/em> <strong>2024<\/strong>, <em>15<\/em> (1), 1\u201310. https:\/\/doi.org\/10.1038\/s41467-024-49514-4.<\/p>\n<p>(65) Ryusei Kano, Koji Oohora, T. H. Photo-Induced Imine Reduction by a Photoredox Biocatalyst Consisting of a Pentapeptide and a Ru Bipyridine Terpyridine Complex. <em>J. Inorg. Biochem.<\/em> <strong>2024<\/strong>, <em>259<\/em> (June), 110984. https:\/\/doi.org\/10.1016\/j.jinorgbio.2024.112657.<\/p>\n<p>(66) Tagami, K.; Nakayama, M.; Kanbara, T.; Cahard, D.; Yajima, T. 10-Phenylphenothiazine-Organophotocatalyzed Bromo-Perfluoroalkylation of Unactivated Olefins. <em>J. Org. Chem.<\/em> <strong>2024<\/strong>, <em>89<\/em> (10), 7084\u20137094. https:\/\/doi.org\/10.1021\/acs.joc.4c00470.<\/p>\n<p>(67) Di Terlizzi, L.; Martinelli, A.; Merli, D.; Protti, S.; Fagnoni, M. Arylazo Sulfones as Nonionic Visible-Light Photoacid Generators. <em>J. Org. Chem.<\/em> <strong>2023<\/strong>, <em>88<\/em> (10), 6313\u20136321. https:\/\/doi.org\/10.1021\/acs.joc.2c01248.<\/p>\n<p>(68) Fortier, L.; Gosset, C.; Lefebvre, C.; Pellegrini, S.; P\u00e9linski, L.; Bousquet, T. Photocatalyzed Synthesis of 3-Substituted Phthalides: A Key Access to (\u00b1)-Herbaric Acid. <em>European J. Org. Chem.<\/em> <strong>2023<\/strong>, <em>26<\/em> (4), 1\u201363. https:\/\/doi.org\/10.1002\/ejoc.202201247.<\/p>\n<p>(69) Laze, L.; Romero, P.; Bosque, I.; Gonzalez-Gomez, J. C. Oxidative Coupling of 4\u2010Hydroxycoumarins with Quinoxalin\u20102 1H \u2010ones Induced by Visible Light. <em>European J. Org. Chem.<\/em> <strong>2023<\/strong>, <em>2<\/em> (Cdc), 125\u2013127. https:\/\/doi.org\/10.2307\/j.ctv1dwq04c.8.<\/p>\n<p>(70) K.Davids, T.; F.Petersen, W.; Smith, G. S. Evaluation of a Trinuclear Heteroleptic Bis-Cyclometalated Iridium(III) Complex as a Photoredox Catalyst for Visible Light-Mediated Hydrothiolation Reactions. <em>Inorg. Chem. Commun.<\/em> <strong>2023<\/strong>.<\/p>\n<p>(71) Erchinger, J. E.; Hoogesteger, R.; Laskar, R.; Dutta, S.; H\u00fcmpel, C.; Rana, D.; Daniliuc, C. G.; Glorius, F. EnT-Mediated N \u2013 S Bond Homolysis of a Bifunctional Reagent Lead- Ing to Aliphatic Sulfonyl Fluorides. <em>J. Am. Chem. Soc<\/em> <strong>2023<\/strong>, ASAP.<\/p>\n<p>(72) Wang, W.; Rondon, B.; Wang, Z.; Wang, J.; Niu, J. Macrocyclic Allylic Sulfone as A Universal Comonomer in Organocatalyzed Photocontrolled Radical Copolymerization with Vinyl Monomers. <em>Macromolecules<\/em> <strong>2023<\/strong>, Accepted. https:\/\/doi.org\/10.1021\/acs.macromol.2c02025.<\/p>\n<p>(73) Liu, C.; Shen, N.; Shang, R. Photocatalytic Defluoroalkylation of Trifluoroacetates with Alkenes Using 4-(Acetamido)Thiophenol. <em>Synthesis (Stuttg).<\/em> <strong>2023<\/strong>.<\/p>\n<p>(74) Chen, X.; Lian, Z.; Kramer, S. Enantioselective Intermolecular Radical Amidation and Amination of Benzylic C \u2212 H Bonds via Dual Copper and Photocatalysis. <em>Angew. Chemie Int. Ed.<\/em> <strong>2023<\/strong>. https:\/\/doi.org\/10.1002\/anie.202217638.<\/p>\n<p>(75) Tan, G.; Paulus, F.; Petti, A.; Wiethoff, M.-A.; Lauer, A.; Daniliuc, C.; Glorius, F. Metal-Free Photosensitized Radical Relay 1,4-Carboimination Across Two Distinct Olefins. <em>Chem. Sci.<\/em> <strong>2023<\/strong>. https:\/\/doi.org\/10.1039\/x0xx00000x.<\/p>\n<p>(76) Michaely, A.; Janka, O.; Gie\u00dfelmann, E. C. J.; Haberkorn, R.; Wiedemann, H. T. A.; Kay, C. W. M.; Kickelbick, G. Black Titania and Niobia within Ten Minutes \u2013 Mechanochemical Reduction of Metal Oxides with Alkali Metal Hydrides. <em>Chem. A Eur. J.<\/em> <strong>2023<\/strong>. https:\/\/doi.org\/10.1016\/s0740-5472(96)90021-5.<\/p>\n<p>(77) Kapil, K.; Jazani, A. M.; Szczepaniak, G.; Murata, H.; Olszewski, M.; Matyjaszewski, K. Fully Oxygen-Tolerant Visible-Light-Induced ATRP of Acrylates in Water\u202f: Toward Synthesis of Protein-Polymer Hybrids. <em>Macromolecules<\/em> <strong>2023<\/strong>, 1\u201314. https:\/\/doi.org\/10.1021\/acs.macromol.2c02537.<\/p>\n<p>(78) Vinayagam, V.; Hajay Kumar, T. V.; Nune, R.; Karre, S. K.; Sadhukhan, S. K. Visible-Light-Promoted Dual Photoredox\/Nickel-Catalyzed Chemoselective Reduction of Secondary and Tertiary Amides with Hydrosilanes in the Presence of an Ester. <em>J. Org. Chem.<\/em> <strong>2023<\/strong>, <em>88<\/em>, 2122\u20132131. https:\/\/doi.org\/10.1021\/acs.joc.2c02543.<\/p>\n<p>(79) Caiger, L.; Zhao, H.; Douglas, J. J.; Leonori, D. The Merger of Aryl Radical-Mediated Halogen-Atom Transfer (XAT) and Copper Catalysis for the Modular Cross-Coupling-Type Functionalization of Alkyl Iodides. <em>ACS Catal.<\/em> <strong>2023<\/strong>, <em>13<\/em>, 4985\u20134991. https:\/\/doi.org\/10.1021\/acscatal.3c00571.<\/p>\n<p>(80) Anwar, K.; Aguilar, J.; Abazid, A. H.; Yarroudi, E.; Funes-ardoiz, I.; G\u00f3mez-su\u00e1rez, A. Modular Synthesis of Polar Spirocyclic Scaffolds Enabled by Radical Chemistry. <em>Org. Lett.<\/em> <strong>2023<\/strong>, 1\u20135.<\/p>\n<p>(81) Mortishire-Smith, B. J.; Becker, S. M.; Simeone, A.; Melidis, L.; Balasubramanian, S. A Photoredox Reaction for the Selective Modification of 5-Carboxycytosine in DNA. <em>J. Am. Chem. Soc.<\/em> <strong>2023<\/strong>, <em>145<\/em> (19), 10505\u201310511. https:\/\/doi.org\/10.1021\/jacs.2c12558.<\/p>\n<p>(82) Mathew M. Simpson, Ching Ching Lam, Jonathan M. Goodman, and S. B. Selective Functionalisation of 5\u2010Methylcytosine by Organic Photoredox Catalysis. <em>Angew. Chem. Int. Ed. Engl.<\/em> <strong>2023<\/strong>.<\/p>\n<p>(83) Venditto, N. J.; Boerth, J. A. Photoredox-Catalyzed Multicomponent Synthesis of Functionalized \u03b3-Amino Butyric Acids via Reductive Radical Polar Crossover. <em>Org. Lett.<\/em> <strong>2023<\/strong>. https:\/\/doi.org\/10.1021\/acs.orglett.3c00991.<\/p>\n<p>(84) Chattapadhyay, D.; Aydogan, A.; Doktor, K.; Maity, A.; Wu, J. W.; Michaudel, Q. Harnessing Sulfur(VI) Fluoride Exchange Click Chemistry and Photocatalysis for Deaminative Benzylic Arylation. <em>ACS Catal.<\/em> <strong>2023<\/strong>, <em>13<\/em> (Vi), 7263\u20137268. https:\/\/doi.org\/10.1021\/acscatal.3c01981.<\/p>\n<p>(85) Koike, T.; Okumura, R.; Kato, T.; Abe, M.; Akita, M. One-Electron Injection-Triggered Radical Reaction of Alkyl Benzoates Promoted by 1,4-Bis(Diphenylamino)Benzene Photocatalysis. <em>ChemCatChem<\/em> <strong>2023<\/strong>, <em>15<\/em> (3), e2022011311.<\/p>\n<p>(86) Kommedal, E. G.; Angeltveit, C. F.; Klau, L. J.; Ayuso-Fern\u00e1ndez, I.; Antonsen, S. G.; Stenstr\u00f8m, Y.; Ekeberg, D.; G\u00edrio, F.; Horn, S. J.; Aachmann, F. L.; Eijsink, V. G. H. H. Visible Light-Exposed Lignin Facilitates Cellulose Solubilization by Lytic Polysaccharide Monooxygenases. <em>Nat. Commun.<\/em> <strong>2023<\/strong>, <em>14<\/em> (1). https:\/\/doi.org\/10.1038\/s41467-023-36660-4.<\/p>\n<p>(87) Tozawa, K.; Makino, K.; Tanaka, Y.; Nakamura, K.; Inagaki, A.; Tabata, H.; Oshitari, T.; Natsugari, H.; Kuroda, N.; Kanemaru, K.; Oda, Y.; Takahashi, H. Conversion of Racemic Alkyl Aryl Sulfoxides into Pure Enantiomers Using a Recycle Photoreactor: Tandem Use of Chromatography on Chiral Support and Photoracemization on Solid Support. <em>J. Org. Chem.<\/em> <strong>2023<\/strong>, <em>2<\/em> (1), 1\u20135. https:\/\/doi.org\/10.1021\/acs.joc.3c00265.<\/p>\n<p>(88) Kleinmans, R.; Dutta, S.; Ozols, K.; Shao, H.; Sch\u00e4fer, F.; Thielemann, R. E.; Chan, H. T.; Daniliuc, C. G.; Houk, K. N.; Glorius, F. Ortho-Selective Dearomative [2\u03c0 + 2\u03c3] Photocycloadditions of Bicyclic Aza-Arenes. <em>J. Am. Chem. Soc<\/em> <strong>2023<\/strong>.<\/p>\n<p>(89) Auvray, M.; Jeanty, M.; Jubault, P.; Poisson, T. Photoinduced Minisci Reaction with Diazines: An Approach Toward Original Fused Heterocycles. <em>Chem. A Eur. J.<\/em> <strong>2023<\/strong>, 1\u2013115. https:\/\/doi.org\/10.1016\/s0740-5472(96)90021-5.<\/p>\n<p>(90) Geniller, L.; Taillefer, M.; Jaroschik, F.; Prieto, A. Photo-Induced Formal Trifluoropropanation of Organic Halides. <em>ACS Catal.<\/em> <strong>2023<\/strong>, <em>13<\/em>.<\/p>\n<p>(91) Baleeva, N. S.; Smirnov, A. Y.; Zaitseva, E. R.; Ivanov, D. S.; Sokolov, A. I.; Mikhaylov, A. A.; Myasnyanko, I. N.; Baranov, M. S. Photoinduced [1,5]-Hydride Shift Triggered Cyclization. <em>New J. Chem.<\/em> <strong>2023<\/strong>.<\/p>\n<p>(92) Wang, H.; Shao, H.; Das, A.; Dutta, S.; Chan, H. T.; Daniliuc, C.; Houk, K. N.; Glorius, F. Dearomative Ring Expansion of Thiophenes by Bicyclobutane Insertion. <em>Science (80-. ).<\/em> <strong>2023<\/strong>, <em>381<\/em> (75). https:\/\/doi.org\/10.1126\/science.adh9737.<\/p>\n<p>(93) Wang, H.; Liu, Z.; Das, A.; Bellotti, P.; Megow, S.; Temps, F.; Qi, X.; Glorius, F. Radical Thioesterification via Nickel-Catalysed Sensitized Electron Transfer. <em>Nat. Synth.<\/em> <strong>2023<\/strong>. https:\/\/doi.org\/10.1038\/s44160-023-00353-z.<\/p>\n<p>(94) Kramp, H.; Weck, R.; Sandvoss, M.; Sib, A.; Mencia, G.; Fazzini, P.-F.; Chaudret, B.; Derdau, V. In-Situ Generated Iridium Nanoparticles as Hydride Donors in Photoredox-Catalyzed Hydrogen-Isotope Exchange Reactions with Deuterium and Tritium Gas. <em>Angew. Chemie &#8211; Int. Ed.<\/em> <strong>2023<\/strong>, <em>62<\/em> (36).<\/p>\n<p>(95) Lee, J. C.; Cuthbertson, J. D.; Mitchell, N. J. Chemoselective Late-Stage Functionalization of Peptides via Photocatalytic C2-Alkylation of Tryptophan. <em>Org. Lett.<\/em> <strong>2023<\/strong>. https:\/\/doi.org\/10.1021\/acs.orglett.3c01795.<\/p>\n<p>(96) Lapierre, R.; Le, T. M. T.; Schiavi, B.; Thevenet, D.; Bazin, M.; Buzdygon, R.; Jubault, P.; Poisson, T. Photocatalytic and Photoinduced Phosphonylation of Aryl Iodides: A Batch and Flow Study. <em>Org. Process Res. Dev.<\/em> <strong>2023<\/strong>. https:\/\/doi.org\/10.1021\/acs.oprd.2c00379.<\/p>\n<p>(97) Peshkov, A. A.; Gapanenok, D.; Puzyk, A.; Amire, N.; Novikova, A. S.; Martynova, S. D.; Kalinina, S.; Dar\u2019in, D.; Peshkov, V. A.; Krasavina, M. Substrate-Controlled Three-Component Synthesis of Diverse Fused Heterocycles. <em>J. Org. Chem.<\/em> <strong>2023<\/strong>.<\/p>\n<p>(98) Niggli, N. E.; Bienewald, F.; Kirchner, H.; Shevchenko, G. A.; Hashmi, A. S. K.; Schaub, T. Synthesis of 1,2-Dialkylaminoethers via Photoredox Catalyzed Hydroamination of Vinylethers. <em>ChemistrySelect<\/em> <strong>2023<\/strong>, <em>8<\/em> (26). https:\/\/doi.org\/10.1002\/slct.202302093.<\/p>\n<p>(99) Hu, T.; Jaber, M.; Bouyssi, D.; Monteiro, N.; Amgoune, A. Photoinduced NiH Catalysis with Trialkylamines for the Stereodivergent Transfer Semi-Hydrogenation of Alkynes. <em>Chem. A Eur. J.<\/em> <strong>2023<\/strong>, 1\u201375.<\/p>\n<p>(100) Li, X.; Dolbier, W. Visible-Light-Induced Three-Component Tetrafluoroethyl-Heteroarylation of Alkenes with 1,1,2,2-Tetrafluoroethanesulfonyl Chloride and Quinoxalin-2(1H)-Ones. <em>Chem. A Eur. J.<\/em> <strong>2023<\/strong>.<\/p>\n<p>(101) Russo, C.; Donati, G.; Giustiniano, F.; Amato, J.; Marinelli, L.; Whitby, R. J.; Mariateresa, G. Isocyanides as Catalytic Electron Acceptors in the Visible Light Promoted Oxidative Formation of Benzyl and Acyl Radicals. <em>Chem. A Eur. J.<\/em> <strong>2023<\/strong>.<\/p>\n<p>(102) Sarkar, S.; Ghosh, S.; Kurandina, D.; Noffel, Y.; Gevorgyan, V. Enhanced Excited-State Hydricity of Pd-H Allows for Unusual Head-to-Tail Hydroalkenylation of Alkenes. <em>J. Am. Chem. Soc.<\/em> <strong>2023<\/strong>. https:\/\/doi.org\/10.1021\/jacs.3c02410.<\/p>\n<p>(103) Herrick, R. M.; Abd El-Gaber, M. K.; Coy, G.; Altman, R. A. A Diselenide Additive Enables Photocatalytic Hydroalkoxylation of Gem-Difluoroalkenes. <em>Chem. Commun.<\/em> <strong>2023<\/strong>, <em>59<\/em> (37), 5623\u20135626. https:\/\/doi.org\/10.1039\/d3cc01012k.<\/p>\n<p>(104) Cvek, M.; Jazani, A. M.; Sobieski, J.; Jamatia, T.; Matyjaszewski, K. Comparison of Mechano- and PhotoATRP with ZnO Nanocrystals. <em>Macromolecules<\/em> <strong>2023<\/strong>, 1\u201315. https:\/\/doi.org\/10.1021\/acs.macromol.3c00250.<\/p>\n<p>(105) Shen, N.; Liu, C.; Zhang, X.; Shang, R. O\u2011Phosphinodiarylamides as Reductive Photocatalysts for Dehalogenative and Deaminative Cross-Couplings. <em>ACS Catal.<\/em> <strong>2023<\/strong>. https:\/\/doi.org\/10.1021\/acscatal.3c03569.<\/p>\n<p>(106) Yukiya, S.; Miyamoto, Y.; Matsui, T.; Sumida, Y.; Ohmiya, H. Diastereoselective Congested \u03b2-Amido Ketone Synthesis via NHC-Catalyzed Radical-Radical Coupling. <em>Chem Catal.<\/em> <strong>2023<\/strong>. https:\/\/doi.org\/https:\/\/doi.org\/10.1016\/j.checat.2023.100736.<\/p>\n<p>(107) Shoya Nohara , Suguru Iwai , Naoya Yamaguchi , Yosuke Asada , Yusuke Kamiyama , Yuta Tanaka , Kenta Tanaka, Y. H. Visible-Light-Induced Oxidative Generation of o-Quinone Methides for Inverse-Electron-Demand [4+2] Cycloaddition Reactions. <em>Synlett<\/em> <strong>2023<\/strong>.<\/p>\n<p>(108) Kvasovs, N.; Fang, J.; Kliuev, F.; Gevorgyan, V. Merging of Light\/Dark Palladium Catalytic Cycles Enables Multicomponent Tandem Alkyl Heck\/Tsuji-Trost Homologative Amination Reaction toward Allylic Amines. <em>J. Am. Chem. Soc.<\/em> <strong>2023<\/strong>. https:\/\/doi.org\/10.1021\/jacs.3c04968.<\/p>\n<p>(109) Qin, J.; Barday, M.; Jana, S.; Sanosa, N.; Funes-Ardoiz, I.; Teskey, C. Couplage r\u00e9ductif de pyridines et de di\u00e8nes induit par photocatalyse au cobalt et rendu possible par un transfert mono\u00e9lectronique coupl\u00e9. <em>Angew. Chemie Int. Ed.<\/em> <strong>2023<\/strong>, <em>202310639<\/em>. https:\/\/doi.org\/10.1002\/anie.202310639.<\/p>\n<p>(110) Laze, L.; Quevedo-flores, B.; Bosque, I.; Gonzalez-gomez, J. C. Couplage d\u00e9shydrog\u00e9nant crois\u00e9 d&rsquo;azaar\u00e8nes avec des alcanes sans m\u00e9taux, sans chlore et sans oxydants sacrificiels. <em>ChemRxiv<\/em> <strong>2023<\/strong>.<\/p>\n<p>(111) Yang, Y.; Miraghaee, S.; Pace, R.; Umemoto, T.; Hammond, G. B. Pr\u00e9paration et \u00e9tude de r\u00e9activit\u00e9 d&rsquo;un agent de trifluorom\u00e9thylthiolation polyvalent : le S-trifluorom\u00e9thyl trifluorom\u00e9thanesulfonothioate (TTST). <em>Angew. Chemie<\/em> <strong>2023<\/strong>, <em>135<\/em> (32). https:\/\/doi.org\/10.1002\/ange.202306095.<\/p>\n<p>(112) Kuehl, N. J.; Taylor, M. T. Trifluorom\u00e9thylation biomol\u00e9culaire rapide utilisant des esters sulfonates aromatiques cationiques comme photocages radicalaires activ\u00e9es par la lumi\u00e8re visible. <em>J. Am. Chem. Soc<\/em> <strong>2023<\/strong>, 1\u20138. https:\/\/doi.org\/10.1021\/jacs.3c08098.<\/p>\n<p>(113) Kim, S.; Choi, H.; Kwak, M.; Seo, Y.; Yoo, D. Photocatalyse induite par la lumi\u00e8re visible pour la synth\u00e8se durable de (\u00b1)-pr\u00e9gabaline utilisant du nitrure de carbone issu d&rsquo;un complexe m\u00e9lamine-acide cyanurique. <em>Nano Trends<\/em> <strong>2023<\/strong>, 100026. https:\/\/doi.org\/10.1016\/j.nwnano.2023.100026.<\/p>\n<p>(114) Laze, L.; Quevedo-flores, B.; Bosque, I.; Gonzalez-gomez, J. C. Alcanes dans une r\u00e9action de type Minisci en conditions photocatalytiques avec d\u00e9gagement d&rsquo;hydrog\u00e8ne. <em>Org. Lett.<\/em> <strong>2023<\/strong>, 1\u2013121. https:\/\/doi.org\/10.1021\/acs.orglett.3c02619.<\/p>\n<p>(115) Fritz Paulus, Colin Stein, Corinna Heusel, Tobias J. Stoffels, Constantin G. Daniliuc, and F. G. 1,2,5-Trifonctionnalisations photochimiques \u00e0 trois composants d&rsquo;alc\u00e8nes vers des lynchpins dens\u00e9ment fonctionnalis\u00e9s. <em>J. Am. Chem. Soc<\/em> <strong>2023<\/strong>.<\/p>\n<p>(116) Wang, H.; Erchinger, J. E.; Lenz, M.; Dutta, S.; Daniliuc, C. G.; Glorius, F. Difonctionnalisation syn-s\u00e9lective de bicyclobutanes rendue possible par clivage de liaison C\u2013S \u03c3 m\u00e9di\u00e9e par photoredox. <em>J. Am. Chem. Soc<\/em> <strong>2023<\/strong>.<\/p>\n<p>(117) Sumin Kim, Jinsol Bok, Byoung-Hoon Lee, Hyunwoo Choi, Youngran Seo, Jiheon Kim, Junhee Kim, Wonjae Ko, Kug-Seung Lee, Sung-Pyo Cho, Taeghwan Hyeon*, and D. Y. Photocatalyse duale orthogonale d&rsquo;atomes isol\u00e9s sur nitrures de carbone pour une transformation organique en relais en un seul pot. <em>J. Am. Chem. Soc<\/em> <strong>2023<\/strong>, 1\u201341.<\/p>\n<p>(118) Patel, S.; Chakraborty, A.; Chatterjee, I. R\u00e9action de couplage crois\u00e9 radicalaire C(sp3)\u2013C(sp3) via photoexcitation. <em>Org. Lett.<\/em> <strong>2023<\/strong>.<\/p>\n<p>(119) Nakashima, Y.; Sumimoto, M.; Nishikata, T. Borylation chimios\u00e9lective d&rsquo;iodoarenes acc\u00e9l\u00e9r\u00e9e par carboxamide sous photoirradiation. <em>Synthesis (Stuttg).<\/em> <strong>2023<\/strong>.<\/p>\n<p>(120) Ermakova, E. V.; Bessmertnykh-Lemeune, A. Complexes de Mg et Zn avec \u03b2-octaph\u00e9nylporphyrine substitu\u00e9e par phosphonate comme photocatalyseurs pour l&rsquo;oxydation de sulfures. <em>Macroheterocycles<\/em> <strong>2023<\/strong>, <em>16<\/em> (2), 117\u2013122. https:\/\/doi.org\/10.6060\/mhc235119l.<\/p>\n<p>(121) Roy, S.; Biswas, A.; Paul, H.; Chatterjee, I. Introduction de N-sulfinylamines dans la chimie des carb\u00e8nes induite par la lumi\u00e8re visible. <em>Org. Lett.<\/em> <strong>2023<\/strong>.<\/p>\n<p>(122) Cywar, R. M.; Ling, C.; Clarke, R. W.; Kim, D. H.; Kneucker, C. M.; Salvach\u00faa, D.; Addison, B.; Hesse, S. A.; Takacs, C. J.; Xu, S.; Demirtas, M. U.; Woodworth, S. P.; Rorrer, N. A.; Johnson, C. W.; Tassone, C. J.; Allen, R. D.; Chen, E. Y.; Beckham, G. T. Vitrim\u00e8res \u00e9lastom\u00e8res issus de polyhydroxyalcanoates con\u00e7us avec recyclabilit\u00e9 et biod\u00e9gradabilit\u00e9. <em>Sci. Adv.<\/em> <strong>2023<\/strong>, <em>9<\/em> (47), 1\u201316. https:\/\/doi.org\/10.1126\/sciadv.adi1735.<\/p>\n<p>(123) Donnier-Valentin, L.; Kassamba, S.; Legros, J.; Fressign\u00e9, C.; Vuluga, D.; Brown, R. C. D.; Linclau, B.; Paolis, M. De. Formation photoinduite de thio\u00e9thers aryliques cubyles et synth\u00e8se d&rsquo;un analogue monocubyle de la dapsone. <em>Org. Lett.<\/em> <strong>2023<\/strong>, 1\u201354.<\/p>\n<p>(124) Jazani, A. M.; Rawls, C.; Matyjaszewski, K. Photo-RDRP pour tous : polym\u00e9risation radicalaire par d\u00e9sactivation r\u00e9versible tol\u00e9rante \u00e0 l&rsquo;oxyg\u00e8ne induite par la lumi\u00e8re de smartphone. <em>Eur. Polym. J.<\/em> <strong>2023<\/strong>, 112631. https:\/\/doi.org\/10.1016\/j.eurpolymj.2023.112631.<\/p>\n<p>(125) Nicolas Joly, Alessandro Colella, Monique-Edwige Mendy, Mbaye Diagne Mbaye, Sylvain Gaillard, Albert Poater, J.-L. R. Synth\u00e8se de c\u00e9tones \u03b3,\u03b4-insatur\u00e9es catalys\u00e9e par le fer induite par la lumi\u00e8re bleue. <em>ChemSusChem<\/em> <strong>2023<\/strong>.<\/p>\n<p>(126) Geniller, L.; Taillefer, M.; Jaroschik, F.; Prieto, A. Amination photocatalys\u00e9e d&rsquo;halog\u00e9nures d&rsquo;alkyle pour acc\u00e9der aux amines primaires. <em>J. Org. Chem.<\/em> <strong>2023<\/strong>, 1\u201335.<\/p>\n<p>(127) Archer, G.; Meyrelles, R.; Eder, I.; Kov\u00e1cs, N.; Maryasin, B.; M\u00e9debielle, M.; Merad, J. Monoalkylation \u03b1-C-H catalys\u00e9e par photoredox de polyols sym\u00e9triques en pr\u00e9sence de CO2. <em>Angew. Chemie Int. Ed.<\/em> <strong>2023<\/strong>. https:\/\/doi.org\/10.1002\/anie.202315329.<\/p>\n<p>(128) Lorenzo Di Terlizzi, Luca Nicchio, Camilla Callegari, Simone Scaringi, Luc Neuville, Maurizio Fagnoni, S. P. G. M. Difonctionnalisation vicinale divergente et r\u00e9gios\u00e9lective de styr\u00e8nes avec des arylazo sulfones m\u00e9di\u00e9e par la lumi\u00e8re visible. <em>Org. Lett.<\/em> <strong>2023<\/strong>.<\/p>\n<p>(129) Akulov, A. A.; Varaksin, M. V.; Nelyubina, A. A.; Tsmokaluk, A. N.; Mazhukin, D. G.; Tikhonov, A. Y.; Charushin, V. N.; Chupakhin, O. N. Amination C\u2013H radicalaire catalys\u00e9e par l&rsquo;iode d&rsquo;oxydes d&rsquo;imidazole non aromatiques : acc\u00e8s aux \u03b1-aminonitrones cycliques. <em>J. Org. Chem.<\/em> <strong>2023<\/strong>. https:\/\/doi.org\/10.1021\/acs.joc.3c02230.<\/p>\n<p>(130) Rivas, M.; Debnath, S.; Giri, S.; Noffel, Y. M.; Sun, X.; Gevorgyan, V. Carboradiofluoration formelle d&rsquo;alc\u00e8nes en un seul pot : une bo\u00eete \u00e0 outils pour le d\u00e9veloppement de sondes d&rsquo;imagerie par tomographie par \u00e9mission de positons. <em>J. Am. Chem. Soc.<\/em> <strong>2023<\/strong>, <em>145<\/em> (35), 19265\u201319273. https:\/\/doi.org\/10.1021\/jacs.3c04548.<\/p>\n<p>(131) Mahmoud, E. M.; Iwasaki, H.; Hada, K.; Murata, Y.; Sumii, Y.; Shibata, N. Synth\u00e8se de pyridine-SF4-alcynes via couplage radicalaire promu par la lumi\u00e8re de pyridine-SF4-chlorures et de r\u00e9actifs EBX. <em>Bull. Chem. Soc. Jpn.<\/em> <strong>2023<\/strong>, <em>96<\/em> (2), 110\u2013112. https:\/\/doi.org\/10.1246\/bcsj.20220330.<\/p>\n<p>(132) Mayerhofer, V. J.; Lippolis, M.; Teskey, C. J. Couplage r\u00e9ductif intermol\u00e9culaire de di\u00e8nes et de c\u00e9tones \u00e0 double catalyse. <em>Angew. Chemie &#8211; Int. Ed.<\/em> <strong>2023<\/strong>. https:\/\/doi.org\/10.1002\/anie.202314870.<\/p>\n<p>(133) Dasi, R.; Villinger, A.; Brasholz, M. Photocycloadditions [2 + 2] et [3 + 2] de 2-cyanochromone avec des alc\u00e8nes sensibilis\u00e9es par l&rsquo;iridium(III) induites par la lumi\u00e8re visible. <em>Org. Biomol. Chem.<\/em> <strong>2023<\/strong>, <em>21<\/em> (30), 6103\u20136106. https:\/\/doi.org\/10.1039\/d3ob00862b.<\/p>\n<p>(134) Goto, Y.; Sano, M.; Sumida, Y.; Ohmiya, H. Acylation organique d&rsquo;ar\u00e8nes riches en \u00e9lectrons catalys\u00e9e par carb\u00e8ne N-h\u00e9t\u00e9rocyclique. <em>Nat. Synth.<\/em> <strong>2023<\/strong>, <em>2<\/em>, 1037\u20131045.<\/p>\n<p>(135) Ben-Hadj-Salem, J.; Dragoe, D.; Marie, P.; Froissart, S.; Fouchet, A.; Rouden, J.; Lecourt, J.; Harnois, C.; Touil, S.; Baudoux, J.; Lepoittevin, B. Acide amido bisphosphonique comme agent d&rsquo;ancrage et initiateur de photopolym\u00e9risation sur surface d&rsquo;oxyde de zirconium. <em>Eur. Polym. J.<\/em> <strong>2023<\/strong>, <em>195<\/em>. https:\/\/doi.org\/10.1016\/j.eurpolymj.2023.112207.<\/p>\n<p>(136) Miura, T.; Yoritate, M.; Hirai, G. C-Glycosylation sans groupe protecteur catalys\u00e9e par photoredox avec sulfinate de glycosyle via la r\u00e9action de Giese. <em>Chem. Commun.<\/em> <strong>2023<\/strong>, <em>59<\/em> (55), 8564\u20138567. https:\/\/doi.org\/10.1039\/d3cc02361c.<\/p>\n<p>(137) Williams, J. D.; Leach, S. G.; Kerr, W. J. Approche umpolung vers les amides 1,4-dicarbonyl\u00e9s acycliques via des radicaux carbamoyles g\u00e9n\u00e9r\u00e9s par photoredox. <em>Chem. &#8211; A Eur. J.<\/em> <strong>2023<\/strong>, <em>29<\/em> (28). https:\/\/doi.org\/10.1002\/chem.202300403.<\/p>\n<p>(138) Candish, L.; Collins, K. D.; Cook, G. C.; Douglas, J. J.; G\u00f3mez-Su\u00e1rez, A.; Jolit, A.; Keess, S. Photocatalyse dans l&rsquo;industrie des sciences de la vie. <em>Chem. Rev.<\/em> <strong>2022<\/strong>, <em>122<\/em> (2), 2907\u20132980. https:\/\/doi.org\/10.1021\/acs.chemrev.1c00416.<\/p>\n<p>(139) Griffiths, R. C.; Smith, F. R.; Long, J. E.; Williams, H. E. L.; Oldham, N. J.; Layfield, R.; Mitchell, N. J. Installation s\u00e9lective de site de cha\u00eenes lat\u00e9rales modifi\u00e9es en Ne dans des peptides et prot\u00e9ines via formation de liaison C-C d\u00e9sulfurative m\u00e9di\u00e9e par la lumi\u00e8re visible. <em>Angew. Chem. Int. Ed. Angew. Chem<\/em> <strong>2022<\/strong>, <em>61<\/em> (2), e202110223.<\/p>\n<p>(140) Gravatt, C. S.; Johannes, J. W.; Ghosh, A. Trifluorom\u00e9thylthiolation d&rsquo;iodures aryliques et h\u00e9t\u00e9roaryliques catalys\u00e9e par le nickel et m\u00e9di\u00e9e par photoredox. <em>Chem Rxiv<\/em> <strong>2022<\/strong>, No. 0.<\/p>\n<p>(141) Cannalire, R.; Santoro, F.; Russo, C.; Graziani, G.; Tron, G. C.; Carotenuto, A.; Brancaccio, D.; Giustiniano, M. Synth\u00e8se d&rsquo;amides \u00e0 partir d&rsquo;isocyanures catalys\u00e9e par photomicelles : optimisation, port\u00e9e et \u00e9tudes RMN des interactions photocatalyseur\/tensioactif. <em>ACS Org. Inorg. Au<\/em> <strong>2022<\/strong>, <em>2<\/em> (1), 66\u201374. https:\/\/doi.org\/10.1021\/acsorginorgau.1c00028.<\/p>\n<p>(142) Hyodo, Y.; Takahashi, K.; Chitose, Y.; Abe, M.; Yoshizawa, M.; Koike, T.; Akita, M. Assemblages de 1,4-bis(diarylamino)naphtal\u00e8nes et d&rsquo;amphiphiles aromatiques : catalyse photoredox hautement r\u00e9ductrice dans l&rsquo;eau. <em>Synlett<\/em> <strong>2022<\/strong>, <em>33<\/em>, 1184\u20131188. https:\/\/doi.org\/10.1055\/a-1652-2707.<\/p>\n<p>(143) Huang, H.-M.; Bellotti, P.; Chen, P.-P.; Houk, K. N.; Glorius, F. Arylation C(sp3)\u2013H allylique d&rsquo;ol\u00e9fines via catalyse ternaire. <em>Nat. Synth.<\/em> <strong>2022<\/strong>, <em>1<\/em> (1), 59\u201368. https:\/\/doi.org\/10.1038\/s44160-021-00006-z.<\/p>\n<p>(144) J.-H. Ye, P. Bellotti, C. Heusel, F. G. Fonctionnalisations d\u00e9fluorinatives d&rsquo;amides et d&rsquo;esters aliphatiques polyfluor\u00e9s catalys\u00e9es par photoredox. <em>Angew. Chem. Int. Ed.<\/em> <strong>2022<\/strong>, <em>61<\/em>, ASAP.<\/p>\n<p>(145) Huang, H.; Bellotti, P.; Erchinger, J. E.; Paulisch, O.; Glorius, F. Arylation umpolung radicalaire de carbonyles via double catalyse au nickel. <em>J. Am. Chem. Soc.<\/em> <strong>2022<\/strong>. https:\/\/doi.org\/10.1021\/jacs.1c12199.<\/p>\n<p>(146) Liu, C.; Shen, N.; Shang, R. D\u00e9fluoroalkylation et hydrod\u00e9fluoration photocatalytiques de trifluorom\u00e9thyles utilisant l&rsquo;O-phosphinoph\u00e9nolate. <em>Nat. Commun.<\/em> <strong>2022<\/strong>, <em>13<\/em> (1), 1\u20138. https:\/\/doi.org\/10.1038\/s41467-022-28007-2.<\/p>\n<p>(147) Jacob, C.; Baguia, H.; Dubart, A.; Thilmany, P.; Oger, S.; Deldaele, C.; Beaudelot, J.; Michelet, B.; Perusk\u00f8, S.; Romero, E.; Moucheron, C.; Theunissen, C.; Evano, G. Synth\u00e8se g\u00e9n\u00e9rale d&rsquo;az\u00e9tidines par cyclisation radicalaire anti-Baldwin photoinduite catalys\u00e9e par le cuivre d&rsquo;ynamides. <em>Nat. Commun.<\/em> <strong>2022<\/strong>, <em>13<\/em> (Article number 560), 1\u20138. https:\/\/doi.org\/10.1038\/s41467-022-28098-x.<\/p>\n<p>(148) Quach, L.; Dutta, S.; Philipp, M. P.; Sandfort, F.; Bellotti, P.; Glorius, F. Hydrooxyg\u00e9nation d&rsquo;alc\u00e8nes non activ\u00e9s initi\u00e9e par la lumi\u00e8re visible &#8211; une strat\u00e9gie pour l&rsquo;hydrofonctionnalisation anti-Markovnikov. <em>ACS Catal.<\/em> <strong>2022<\/strong>. https:\/\/doi.org\/10.1021\/acscatal.1c05555.<\/p>\n<p>(149) Shen, N.; Li, R.; Liu, C.; Shen, X.; Guan, W.; Shang, R. Couplages crois\u00e9s photocatalytiques d&rsquo;halog\u00e9nures aryliques rendus possibles par o-phosphinoph\u00e9nolate et o-phosphinothioph\u00e9nolate. <em>ACS Catal.<\/em> <strong>2022<\/strong>, <em>2<\/em> (1), 1\u20135. https:\/\/doi.org\/10.1021\/acscatal.1c05941.<\/p>\n<p>(150) Charlie Swan, Lorenzo Maggi, Mahri Park, Sophie Taylor, William Shepherd, L. T. B. G\u00e9n\u00e9ration de radicaux thiyles \u00e0 partir de substituts de thioph\u00e9nol stables \u00e0 l&rsquo;air et inodores : application au couplage crois\u00e9 C-S promu par la lumi\u00e8re visible. <em>Synthesis (Stuttg).<\/em> <strong>2022<\/strong>. https:\/\/doi.org\/10.1055\/s-00.<\/p>\n<p>(151) Lindroth, R.; Ondrejkov, A.; Wallentin, C. Fragmentation oxydative d&rsquo;\u00e9thers et d&rsquo;ac\u00e9tals m\u00e9di\u00e9e par la lumi\u00e8re visible au moyen de catalyse au Fe(III). <em>Org. Lett.<\/em> <strong>2022<\/strong>. https:\/\/doi.org\/10.1021\/acs.orglett.2c00231.<\/p>\n<p>(152) Zhao, H.; Caldora, H. P.; Turner, O.; Douglas, James, J.; Leonori, D. Approche d\u00e9saturative pour la synth\u00e8se d&rsquo;ald\u00e9hydes aromatiques via triple catalyse synergique \u00e9namine, photoredox et cobalt. <em>Angew. Chem. Int. Ed.<\/em> <strong>2022<\/strong>. https:\/\/doi.org\/10.1002\/anie.202201870.<\/p>\n<p>(153) Oshinowo, M.; Runge, J. R.; Piccini, M.; Marken, F.; Buchard, A. Polyester r\u00e9ticul\u00e9 \u00e0 base de xylose comme \u00e9lectrolyte polym\u00e8re solide biosourc\u00e9 et d\u00e9gradable pour la conduction d&rsquo;ions Li+. <em>J. Mater. Chem. A<\/em> <strong>2022<\/strong>, 23\u201330. https:\/\/doi.org\/10.1039\/d1ta10111k.<\/p>\n<p>(154) Spitz, C.; Bertrand, M.; Remusat, V.; Terme, T.; Vanelle, P. Addition d&rsquo;halog\u00e9nures de benzyle \u00e0 des ald\u00e9hydes et imines utilisant le TDAE photoactiv\u00e9 : acc\u00e8s aux 3,4-dihydroisocoumarines, 1,2-diaryl\u00e9thanol et 1,2-diarylcarbamates en conditions sans m\u00e9taux. <em>J. Org. Chem.<\/em> <strong>2022<\/strong>, <em>2<\/em> (1), 1\u20135. https:\/\/doi.org\/10.1021\/acs.joc.2c00074.<\/p>\n<p>(155) Kleindmans, R.; Pinkert, T.; Dutta, S.; Paulisch, T. O.; Keum, H.; Daniliuc, C. G.; Glorius, F. [2\u03c0+2\u03c3]-Photocycloaddition intermol\u00e9culaire rendue possible par transfert d&rsquo;\u00e9nergie triplet. <em>Nature<\/em> <strong>2022<\/strong>, 69. https:\/\/doi.org\/10.1038\/s41586-022-04636-x.<\/p>\n<p>(156) Can Liu, Kang Li, R. S. Ar\u00e8nethiolate comme catalyseur \u00e0 double fonction pour la d\u00e9fluoroalkylation et l&rsquo;hydrod\u00e9fluoration photocatalytiques de trifluorom\u00e9thyles. <em>ACS Catal.<\/em> <strong>2022<\/strong>, <em>12<\/em> (1), Asap.<\/p>\n<p>(157) Cao, Y. X.; Zhu, G.; Li, Y.; Le Breton, N.; Gourlaouen, C.; Choua, S.; Boixel, J.; Jacquot De Rouville, H. P.; Soul\u00e9, J. F. Arylation photoinduite de sels d&rsquo;acridinium : photocatalyseurs redox ajustables pour le clivage de liaison C-O. <em>J. Am. Chem. Soc.<\/em> <strong>2022<\/strong>, <em>144<\/em> (13), 5902\u20135909. https:\/\/doi.org\/10.1021\/jacs.1c12961.<\/p>\n<p>(158) Roy, S.; Chatterjee, I. Fonctionnalisation (sp3)C\u03b1\u2212H d&rsquo;\u00e9thers m\u00e9di\u00e9e par la lumi\u00e8re visible rendue possible par un complexe donneur-accepteur d&rsquo;\u00e9lectrons. <em>ACS Org. Inorg. Au<\/em> <strong>2022<\/strong>, ASAP. https:\/\/doi.org\/10.1021\/acsorginorgau.2c00008.<\/p>\n<p>(159) Hoopes, C. R.; Garcia, F. J.; Sarkar, A. M.; Kuehl, N. J.; Barkan, D. T.; Nicole, L.; Hsu, C.; Jones, M. D.; Taylor, M. T. Sels de pyridinium donneur-accepteur pour la modification photoinduite par transfert d&rsquo;\u00e9lectrons du tryptophane dans les peptides, prot\u00e9ines et prot\u00e9omes utilisant la lumi\u00e8re visible. <em>J. Am. Chem. Soc<\/em> <strong>2022<\/strong>, ASAP. https:\/\/doi.org\/10.1021\/jacs.1c10536.<\/p>\n<p>(160) Tobias Biberger, Nils N\u00f6thling, Markus Leutzsch, Christopher P. Gordon, Christophe Cop\u00e9ret, and A. F. Complexe dihydrog\u00e8ne dinucl\u00e9aire anionique de ruth\u00e9nium pertinent pour l&rsquo;hydrog\u00e9nation gem d&rsquo;alcynes. <em>Angew. Chem. Int. Ed.<\/em> <strong>2022<\/strong>, asap. https:\/\/doi.org\/10.1002\/anie.202201311.<\/p>\n<p>(161) Archer, G.; Caval\u00e8re, P.; M\u00e9debielle, M.; Merad, J. G\u00e9n\u00e9ration photoredox de cations radicalaires isothiouronyles : une nouvelle plateforme en catalyse radicalaire covalente. <em>Angew. Chem. Int. Ed.<\/em> <strong>2022<\/strong>. https:\/\/doi.org\/10.1002\/anie.2021XXXXX.<\/p>\n<p>(162) Ma, J.; Chen, S.; Bellotti, P.; Wagener, T.; Daniliuc, C.; Houk, K. N.; Glorius, F. Acc\u00e8s facile aux cycles 2D\/3D fusionn\u00e9s via r\u00e9actions de [2 + 2] cycloaddition\/r\u00e9arrangement d\u00e9aromatisantes en cascade intermol\u00e9culaires de quinol\u00e9ines avec des alc\u00e8nes. <em>Nat. Catal.<\/em> <strong>2022<\/strong>, <em>5<\/em> (5), 405\u2013413. https:\/\/doi.org\/10.1038\/s41929-022-00784-5.<\/p>\n<p>(163) Suga, M.; Makino, K.; Tabata, H.; Oshitari, T.; Natsugari, H.; Takahashi, H. Photoisom\u00e9risation du sulindac et du chlorhydrate d&rsquo;ozagrel par catalyseur \u00e0 la vitamine B2 sous irradiation de lumi\u00e8re visible. <em>Pharm. Res.<\/em> <strong>2022<\/strong>, <em>39<\/em>, 577\u2013586.<\/p>\n<p>(164) Annibaletto, J.; Jacob, C.; Theunissen, C. Sels d&rsquo;ammonium comme pr\u00e9curseurs radicalaires pratiques utilisant la catalyse photoredox \u00e0 l&rsquo;iridium. <em>Org. Lett.<\/em> <strong>2022<\/strong>. https:\/\/doi.org\/10.1021\/acs.orglett.2c01407.<\/p>\n<p>(165) Huang, H.; Bellotti, P.; Kim, S.; Zhang, X.; Glorius, F. R\u00e9action multicomposants catalytique impliquant un radical de type c\u00e9tyle. <em>Nat. Synth.<\/em> <strong>2022<\/strong>.<\/p>\n<p>(166) Gapanenok, D.; Makhmet, A.; Peshkov, A. A.; Smirnova, D.; Amire, N.; Peshkov, V. A.; Spiridonova, D.; Dar&rsquo;in, D.; Balalaie, S.; Krasavin, M. Assemblage multicomposants d&rsquo;imidazoles trisubstitu\u00e9s et leur cyclisation photochimique en \u00e9chafaudages polyh\u00e9t\u00e9rocycliques fusionn\u00e9s. <em>J. Org. Chem.<\/em> <strong>2022<\/strong>, <em>87<\/em> (12), 7838\u20137851.<\/p>\n<p>(167) Tan, G.; Das, M.; Keum, H.; Bellotti, P.; Daniliuc, C.; Glorius, F. Synth\u00e8se photochimique en une seule \u00e9tape de d\u00e9riv\u00e9s d&rsquo;acides \u03b2-amin\u00e9s \u00e0 partir d&rsquo;alc\u00e8nes et d'(h\u00e9t\u00e9ro)ar\u00e8nes. <em>Nat. Chem.<\/em> <strong>2022<\/strong>, <em>25<\/em>.<\/p>\n<p>(168) Lindroth, R.; Materna, K. L.; Hammarstr, L.; Wallentin, C. Catalyse Ir-photoredox durable au moyen de l&rsquo;h\u00e9t\u00e9rog\u00e9n\u00e9isation. <em>ACS Org. Inorg. Au<\/em> <strong>2022<\/strong>, 2\u20137. https:\/\/doi.org\/10.1021\/acsorginorgau.2c00024.<\/p>\n<p>(169) Bellotti, P. ; Rogge, T. ; Paulus, F. ; Laskar, R. ; Rendel, N. ; Ma, J. ; Houk, K. N. ; Glorius, F. Cycloadditions p\u00e9ri-(3 + 2) de quinol\u00e9ines photocatalys\u00e9es par la lumi\u00e8re visible. <em>J. Am. Chem. Soc<\/em> <strong>2022<\/strong>, <em>61<\/em>.<\/p>\n<p>(170) Shinkawa, Y. ; Furutani, T. ; Ikeda, T. ; Yamawaki, M. ; Morita, T. ; Yoshimi, Y. Fonctionnalisation d\u00e9carboxylante de la cha\u00eene lat\u00e9rale des acides aspartique\/glutamique \u00e0 l\u2019aide de catalyseurs photoredox bimol\u00e9culaires. <em>J. Org. Chem.<\/em> <strong>2022<\/strong>.<\/p>\n<p>(171) Sch\u00e4fers, F. ; Dutta, S. ; Kleinmans, R. ; M\u00fcck-Lichtenfeld, C. ; Glorius, F. Addition asym\u00e9trique d\u2019allylsilanes aux ald\u00e9hydes : une approche catalytique double Cr\/photoredox compl\u00e9tant la r\u00e9action de Hosomi\u2013Sakurai. <em>ACS Catal.<\/em> <strong>2022<\/strong>, 12281\u201312290. https:\/\/doi.org\/10.1021\/acscatal.2c03960.<\/p>\n<p>(172) Nemez, D. B. ; Lozada, I. B. ; Braun, J. D. ; Williams, J. A. G. ; Herbert, D. E. Synth\u00e8se et chimie de coordination d\u2019une bipyridine benzannul\u00e9e : 6,6\u2032-biph\u00e9nanthridine. <em>Inorg. Chem.<\/em> <strong>2022<\/strong>, <em>61<\/em> (34), 13386\u201313398. https:\/\/doi.org\/10.1021\/acs.inorgchem.2c01514.<\/p>\n<p>(173) Biswas, S. ; Banerjee, S. ; Shlain, M. A. ; Bardin, A. A. ; Ulijn, R. V ; Nannenga, B. L. ; Rappe, A. M. ; Braunschweig, A. B. Contr\u00f4le photom\u00e9canochimique de la st\u00e9r\u00e9os\u00e9lectivit\u00e9 dans la photodim\u00e9risation [2 + 2] de l\u2019ac\u00e9naphtyl\u00e8ne. <em>Faraday Discuss.<\/em> <strong>2022<\/strong>. https:\/\/doi.org\/10.1039\/d2fd00122e.<\/p>\n<p>(174) Liang, Y. ; Kleinmans, R. ; Daniliuc, C. G. ; Glorius, F. Synth\u00e8se de 2-oxabicyclo[2.1.1]hexanes polysubstitu\u00e9s via un transfert d\u2019\u00e9nergie induit par la lumi\u00e8re visible. <em>J. Am. Chem. Soc<\/em> <strong>2022<\/strong>, <em>2<\/em> (1), 1\u20135. https:\/\/doi.org\/10.1021\/jacs.2c09248.<\/p>\n<p>(175) Sp\u00e4th, J. ; Oddy, M. J. ; Hunter, R. ; Petersen, W. Les radicaux acyles chiraux g\u00e9n\u00e9r\u00e9s par la lumi\u00e8re visible permettent un acc\u00e8s st\u00e9r\u00e9os\u00e9lectif aux oxindoles 3,3-disubstitu\u00e9s : application \u00e0 la synth\u00e8se de la (\u2013) et de la (+) physov\u00e9nine. <em>Synthesis (Stuttg).<\/em> <strong>2022<\/strong>.<\/p>\n<p>(176) Hervieu, C. ; Kirillova, M. S. ; Hu, Y. ; Cuesta-galisteo, S. Arylsulfinylamides chiraux : des r\u00e9actifs tout-en-un pour les aminoarylations d\u2019alc\u00e8nes asym\u00e9triques m\u00e9di\u00e9es par la lumi\u00e8re visible. <em>ChemRxiv. Prepr.<\/em> <strong>2022<\/strong>, 1\u201318.<\/p>\n<p>(177) Kim, S. ; Lee, Y. ; Cho, E. J. Homocouplage s\u00e9lectif photoredox de bromures de propargyle. <em>J. Org. Chem.<\/em> <strong>2022<\/strong>, 0\u20137. https:\/\/doi.org\/10.1021\/acs.joc.2c02063.<\/p>\n<p>(178) Zhang, Z. ; Gevorgyan, V. Hydroalqu\u00e9nylation de mol\u00e9cules sous tension activ\u00e9e par l\u2019hydrure de palladium. <em>J. Am. Chem. Soc<\/em> <strong>2022<\/strong>. https:\/\/doi.org\/10.1021\/jacs.2c09045.<\/p>\n<p>(179) Kvasovs, N. ; Gevorgyan, V. Acc\u00e8s aux isom\u00e8res E illusoires d\u2019\u03b1-ester hydrazones via une alkylation de type Heck catalys\u00e9e par le Pd et induite par la lumi\u00e8re visible. <em>Org. Lett.<\/em> <strong>2022<\/strong>, <em>24<\/em> (23), 4176\u20134181. https:\/\/doi.org\/10.1021\/acs.orglett.2c01409.<\/p>\n<p>(180) Zhang, Z. ; Kvasovs, N. ; Dubrovina, A. ; Gevorgyan, V. Alkyle catalys\u00e9 par le Pd, assist\u00e9 par un acide de Br\u00f8nsted et induit par la lumi\u00e8re visible. <em>Angew. Chem. Int. Ed.<\/em> <strong>2022<\/strong>, <em>61<\/em>.<\/p>\n<p>(181) Duff, L. ; Meakin, H. ; Richardson, A. ; Greener, A. J. ; Smith, G. W. A. ; Chechik, V. ; James, J. Hydroxylation d\u00e9nitrante de nitroar\u00e8nes non activ\u00e9s. <em>ChemRxiv. Prepr.<\/em> <strong>2022<\/strong>, 1\u2013132.<\/p>\n<p>(182) Bellotti, P. ; Huang, H. M. ; Faber, T. ; Laskar, R. ; Glorius, F. Couplage catalytique d\u00e9fluorant c\u00e9tyle-ol\u00e9fine par transfert d\u2019atome d\u2019halog\u00e8ne. <em>Chem. Sci.<\/em> <strong>2022<\/strong>, <em>13<\/em> (26), 7855\u20137862. https:\/\/doi.org\/10.1039\/d2sc02732a.<\/p>\n<p>(183) Babu, S. S. ; Gopinath, P. Addition de sulfonyle en tandem et N-cyclisation chimios\u00e9lective d\u2019o-alc\u00e9nyl aryl ur\u00e9es m\u00e9di\u00e9es par la photo : assemblage direct de dihydroquinazolinones fonctionnalis\u00e9es. <em>J. Org. Chem.<\/em> <strong>2022<\/strong>, <em>87<\/em> (14), 9414\u20139418.<\/p>\n<p>(184) Tan, G. ; Paulus, F. ; Renter, A. ; Lalisse, R. F. ; Daniliuc, C. G. ; Gutierrez, O. ; Glorius, F. Oxyimination-1,4 par relais radicalaire hautement s\u00e9lective de deux ol\u00e9fines \u00e9lectroniquement diff\u00e9renci\u00e9es. <em>J. Am. Chem. Soc<\/em> <strong>2022<\/strong>. https:\/\/doi.org\/10.1021\/jacs.2c09244.<\/p>\n<p>(185) Babu, S. S. ; Varmaa, A. A. ; Gopinath, P. Addition de CF3 en cascade et annulations chimiodivergentes d\u2019ortho-alc\u00e9nyl aryl ur\u00e9es catalys\u00e9es par photoredox. <em>Chem. Commun.<\/em> <strong>2022<\/strong>, <em>58<\/em>, 1990\u20131993.<\/p>\n<p>(186) Kinsella, A. G. ; Tibbetts, J. D. ; Stead, D. ; Cresswell, A. J. Les N-tosylhydrazones comme accepteurs de radicaux alkyles nucl\u00e9ophiles en catalyse photoredox : une br\u00e8ve \u00e9tude de cas sur les r\u00e9actions secondaires possibles. <em>Synth. Commun.<\/em> <strong>2022<\/strong>, <em>52<\/em> (3), 413\u2013423. https:\/\/doi.org\/10.1080\/00397911.2022.2028844.<\/p>\n<p>(187) Dutta, S. ; Erchinger, J. E. ; Sch\u00e4fers, F. ; Das, A. ; Daniliuc, C. G. ; Glorius, F. Synth\u00e8se doublement catalys\u00e9e par le chrome\/photoredox d\u2019alcools \u03b1-benzyliques, d\u2019isochromanones, d\u2019alcools 1,2-oxy et d\u2019alcools 1,2-thio. <em>Angew. Chemie &#8211; Int. Ed.<\/em> <strong>2022<\/strong>, <em>61<\/em> (49), 1\u2013177. https:\/\/doi.org\/10.1002\/anie.202212136.<\/p>\n<p>(188) Wang, W. ; Zhou, Z. ; Sathe, D. ; Tang, X. ; Moran, S. ; Jin, J. ; Haeffner, F. ; Wang, J. ; Niu, J. Copolym\u00e8res statistiques vinyliques d\u00e9gradables via une copolym\u00e9risation radicalaire en cascade par ouverture de cycle photocontr\u00f4l\u00e9e. <em>Angew. Chemie &#8211; Int. Ed.<\/em> <strong>2022<\/strong>, <em>61<\/em> (8), 1\u20139. https:\/\/doi.org\/10.1002\/anie.202113302.<\/p>\n<p>(189) Casadevall, C. ; Arag\u00f3n, J. ; Ca\u00f1ellas, S. ; Peric\u00e0s, M. A. ; Lloret-Fillol, J. ; Caldentey, X. D\u00e9veloppement de plateformes d\u2019exp\u00e9rimentation \u00e0 haut d\u00e9bit avanc\u00e9es pour les r\u00e9actions photocatalytiques. Dans <em>ACS Symposium Series<\/em> ; American Chemical Society, 2022 ; Vol. 1419, pp 145\u2013165.  https:\/\/doi.org\/10.1021\/bk-2022-1419.ch009.<\/p>\n<p>(190) Sun, A. C. ; Stephenson, C. R. J. ; Kennedy, R. T. Photochimie \u00e0 haut d\u00e9bit utilisant la microfluidique en gouttes. Dans <em>ACS Symposium Series<\/em> ; American Chemical Society, 2022 ; Vol. 1419, pp 131\u2013143.  https:\/\/doi.org\/10.1021\/bk-2022-1419.ch008.<\/p>\n<p>(191) Cardinale, L. ; Schmotz, M.-O. W. S. ; Konev, M. O. ; Wangelin, A. J. von. Synth\u00e8se d\u2019amides d\u2019acides \u03b1-amin\u00e9s catalys\u00e9e par photoredox par carbamoylation d\u2019imines. <em>Org. Lett.<\/em> <strong>2022<\/strong>, <em>24<\/em> (2), 506\u2013510.<\/p>\n<p>(192) Bergamaschi, E. ; Mayerhofer, V. J. ; Teskey, C. J. Hydroarylation de styr\u00e8nes catalys\u00e9e par l\u2019hydrure de cobalt et activ\u00e9e par la lumi\u00e8re. <em>ACS Catal.<\/em> <strong>2022<\/strong>, 14806\u201314811. https:\/\/doi.org\/10.1021\/acscatal.2c05109.<\/p>\n<p>(193) Geniller, L. ; Taillefer, M. ; Jaroschik, F. ; Prieto, A. G\u00e9n\u00e9ration de radicaux halog\u00e9nures par transfert d\u2019atome d\u2019halog\u00e8ne photo-induit pour une s\u00e9lectivit\u00e9. <em>Chem. &#8211; A Eur. J.<\/em> <strong>2022<\/strong>, <em>28<\/em>, e2022014.<\/p>\n<p>(194) Georgiou, P. G. ; Kinney, N. L. H. ; Kontopoulou, I. ; Baker, A. N. ; Hindmarsh, S. A. ; Bissoyi, A. ; Congdon, T. R. ; Whale, T. F. ; Gibson, M. I. Les brosses mol\u00e9culaires de poly(alcool vinylique) nucl\u00e9ent la glace. <em>Biomacromolecules<\/em> <strong>2022<\/strong>, 10.1021\/acs.biomac.2c01097. https:\/\/doi.org\/10.1021\/acs.biomac.2c01097.<\/p>\n<p>(195) Geniller, L. ; Taillefer, M. ; Jaroschik, F. ; Prieto, A. La catalyse m\u00e9tallaphotoredox au nickel permettant des r\u00e9actions de couplage crois\u00e9 d\u00e9sulfurant. <em>Adv. Synth. Catal.<\/em> <strong>2022<\/strong>. https:\/\/doi.org\/10.1002\/adsc.202201152.<\/p>\n<p>(196) Tan, G. ; Das, M. ; Kleinmans, R. ; Katzenburg, F. ; Glorius, F. Diamination dissym\u00e9trique activ\u00e9e par transfert d\u2019\u00e9nergie utilisant des pr\u00e9curseurs de radicaux azot\u00e9s bifonctionnels sans pr\u00e9c\u00e9dent. <em>Nat. Catal.<\/em> <strong>2022<\/strong>, 1\u201320.<\/p>\n<p>(197) Lyu, J. ; Claraz, A. ; Retailleau, P. ; Masson, G. Cyclodim\u00e9risations st\u00e9r\u00e9os\u00e9lectives (1+1+4+4) et (4+2) de styrylnaphtols sous irradiation \u00e0 la lumi\u00e8re visible a\u00e9robie et catalyse par acide de Br\u00f8nsted. <em>Org. Biomol. Chem.<\/em> <strong>2022<\/strong>. https:\/\/doi.org\/10.1039\/d2ob01509a.<\/p>\n<p>(198) Sorrentino, J. P. ; Herrick, R. M. ; Abd El-Gaber, M. K. ; Abdelazem, A. Z. ; Kumar, A. ; Altman, R. A. Hydrothiolation co-catalytique g\u00e9n\u00e9rale de gem-difluoroalc\u00e8nes. <em>J. Org. Chem.<\/em> <strong>2022<\/strong>, <em>87<\/em> (24), 16676\u201316690. https:\/\/doi.org\/10.1021\/acs.joc.2c02343.<\/p>\n<p>(199) Temerov, F. ; Baghdadi, Y. ; Rattner, E. ; Eslava, S. Une revue sur les photocatalyseurs \u00e0 base de p\u00e9rovskite d\u2019halog\u00e9nure : facteurs cl\u00e9s et d\u00e9fis. <em>ACS Applied Energy Materials<\/em>. 2022, pp 14605\u201314637.  https:\/\/doi.org\/10.1021\/acsaem.2c02680.<\/p>\n<p>(200) Yin, J. ; Sharma, R. ; Tyndall, J. D. A. ; Grimsey, N. L. ; Vernall, A. J. Synth\u00e8se et caract\u00e9risation d\u2019un prom\u00e9dicament photoactiv\u00e9 du r\u00e9cepteur cannabino\u00efde de type 2. <em>ChemPhotoChem<\/em> <strong>2022<\/strong>, No. 2, 2\u20135. https:\/\/doi.org\/10.1002\/cptc.202200291.<\/p>\n<p>(201) Griffiths, R. C. ; Smith, F. R. ; Li, D. ; Wyatt, J. ; Rogers, D. M. ; Long, J. E. ; Cusin, L. M. L. ; Tighe, P. J. ; Layfield, R. ; Hirst, J. D. ; Muller, M. M. ; Mitchell, N. Modification s\u00e9lective de la cyst\u00e9ine de peptides et de prot\u00e9ines via la formation de liaisons C-C d\u00e9sulfurantes. <em>Chem. A Eurpean J.<\/em> <strong>2022<\/strong>.<\/p>\n<p>(202) Schild, D. J. ; Juliana Bem ; Szczepaniak, G. ; Jazani, A. M. ; Matyjaszewski, K. Polym\u00e9risation radicalaire par transfert d\u2019atomes induite par la lumi\u00e8re bleue activ\u00e9e par le fer et le cuivre. <em>J. Polym. Sci.<\/em> <strong>2022<\/strong>, 1\u20139.<\/p>\n<p>(203) Briand, M. ; Thai, L. D. ; Bourdreux, F. ; Vanthuyne, N. ; Moreau, X. ; Magnier, E. ; Anselmi, E. ; Dagousset, G. Trifluorom\u00e9thylation radicalaire \u00e0 distance : une approche unifi\u00e9e pour la synth\u00e8se s\u00e9lective de compos\u00e9s carbonyles \u03b1,\u03b2-insatur\u00e9s \u03b3-trifluorom\u00e9thyl\u00e9s. <em>Org. Lett.<\/em> <strong>2022<\/strong>, <em>24<\/em> (51), 9375\u20139380. https:\/\/doi.org\/10.1021\/acs.orglett.2c03676.<\/p>\n<p>(204) Gentleman, A. S. ; Lawson, T. ; Ellis, M. G. ; Davis, M. ; Turner-Dore, J. ; Ryder, A. S. H. ; Frosz, M. H. ; Ciaccia, M. ; Reisner, E. ; Cresswell, A. J. ; Euser, T. G. Analyse de Stern-Volmer de l\u2019extinction de la fluorescence d\u2019un photocatalyseur dans des micror\u00e9acteurs \u00e0 fibres \u00e0 cristaux photoniques \u00e0 c\u0153ur creux. <em>Chem. Commun.<\/em> <strong>2022<\/strong>, <em>58<\/em> (75), 10548\u201310551. https:\/\/doi.org\/10.1039\/d2cc03996f.<\/p>\n<p>(205) Balakrishna, B. ; Mossin, S. ; Kramer, S. Homocouplage N-N d\u00e9shydrog\u00e9nant sans m\u00e9tal photo-induit. <em>Chem. Commun.<\/em> <strong>2022<\/strong>, 1\u201373.<\/p>\n<p>(206) Tilby, M. J. ; Dewez, D. F. ; Pantaine, L. R. E. ; Hall, A. ; Mart\u00ednez-Lamenca, C. ; Willis, M. C. Fonctionnalisation photocatalytique tardive de sulfonamides via des interm\u00e9diaires radicaux sulfonyles. <em>ACS Catal.<\/em> <strong>2022<\/strong>, <em>12<\/em> (10), 6060\u20136067. https:\/\/doi.org\/10.1021\/acscatal.2c01442.<\/p>\n<p>(207) Alica Ondrejkov\u00e1, Rickard Lindroth, G\u00f6ran Hilmersson, C.-J. W. ; Department ; Ondrejkov\u00e1, A. ; Lindroth, R. ; Hilmersson, G. ; Wallentin, C. J. Utilisation d\u2019une aiguille comme source de fer dans la g\u00e9n\u00e9ration catalytique photoredox double synergique de radicaux alcoxy. <em>Chem. Commun.<\/em> <strong>2022<\/strong>, <em>58<\/em> (juin), 10241\u201310244. https:\/\/doi.org\/10.1039\/d2cc03262g.<\/p>\n<p>(208) Watanabe, K. ; Kuratsu, A. ; Hashizume, D. ; Niwa, T. ; Hosoya, T. Conjugaison d\u2019amines induite par la lumi\u00e8re rouge par formation de liaisons amides d\u00e9clench\u00e9e par photo-oxydation de 3-acylindolizines. <em>Commun. Chem.<\/em> <strong>2022<\/strong>, <em>5<\/em> (1), 1\u20137. https:\/\/doi.org\/10.1038\/s42004-022-00712-5.<\/p>\n<p>(209) Gorbachev, D. ; Smith, E. ; Argent, S. P. ; Newton, G. N. ; Lam, H. W. Synth\u00e8se de nouveaux opio\u00efdes morphinanes par fonctionnalisation photochimique catalys\u00e9e par le TBADT au niveau du squelette carbon\u00e9. <em>Chem. &#8211; A Eur. J.<\/em> <strong>2022<\/strong>, <em>28<\/em> (50). https:\/\/doi.org\/10.1002\/chem.202201478.<\/p>\n<p>(210) Cheung, K. P. S. ; Fang, J. ; Mukherjee, K. ; Mihranyan, A. ; Gevorgyan, V. Amination C-H allylique intermol\u00e9culaire asym\u00e9trique d\u2019alc\u00e8nes avec des amines aliphatiques. <em>Science (80-. ).<\/em> <strong>2022<\/strong>, <em>378<\/em> (6625), 1207\u20131213. https:\/\/doi.org\/10.1126\/science.abq1274.<\/p>\n<p>(211) Russo, C. ; Graziani, G. ; Cannalire, R. ; Tron, G. C. ; Giustiniano, M. Chimie de type Ugi \u00e0 composants multiples sans m\u00e9tal photocatalytique \u00e0 la lumi\u00e8re visible. <em>Green Chem.<\/em> <strong>2022<\/strong>, <em>24<\/em> (10), 3993\u20134003. https:\/\/doi.org\/10.1039\/d2gc00855f.<\/p>\n<p>(212) Varlet, T. ; Bouchet, D. ; Van Elslande, E. ; Masson, G. Hydroacylation d\u00e9saromatisante d\u2019indoles photocatalys\u00e9e par le d\u00e9catungstate : synth\u00e8se directe de 2-acylindolines. <em>Chem. &#8211; A Eur. J.<\/em> <strong>2022<\/strong>, <em>28<\/em> (56). https:\/\/doi.org\/10.1002\/chem.202201707.<\/p>\n<p>(213) Ahmad, A. ; Georgiou, P. G. ; Pancaro, A. ; Hasan, M. ; Nelissen, I. ; Gibson, M. I. Des nanoparticules d\u2019or glycosyl\u00e9es li\u00e9es \u00e0 un polym\u00e8re recrutent des glycoprot\u00e9ines sialyl\u00e9es dans leur couronne prot\u00e9ique, entra\u00eenant une liaison aux lectines hors cible. <em>Nanoscale<\/em> <strong>2022<\/strong>, <em>14<\/em> (36), 13261\u201313273. https:\/\/doi.org\/10.1039\/d2nr01818g.<\/p>\n<p>(214) Frank, N. ; Nugent, J. ; Shire, B. R. ; Pickford, H. D. ; Rabe, P. ; Sterling, A. J. ; Zarganes-Tzitzikas, T. ; Grimes, T. ; Thompson, A. L. ; Smith, R. C. ; Schofield, C. J. ; Brennan, P. E. ; Duarte, F. ; Anderson, E. A. Synth\u00e8se de bioisost\u00e8res d\u2019ar\u00e8nes m\u00e9ta-substitu\u00e9s \u00e0 partir du [3.1.1]propellane. <em>Nature<\/em> <strong>2022<\/strong>, <em>611<\/em> (7937), 721\u2013726. https:\/\/doi.org\/10.1038\/s41586-022-05290-z.<\/p>\n<p>(215) Merkens, K. ; Sanosa, N. ; Funes-Ardoiz, I. ; Gomez-Suarez, A. Acc\u00e8s aux radicaux \u03b1-amino c\u00e9tyles \u00e0 partir de \u03b2-amino alcools via une catalyse par transfert d\u2019atome d\u2019hydrog\u00e8ne chimios\u00e9lective. <em>ACS Catal.<\/em> <strong>2022<\/strong>, <em>12<\/em> (21), 13186\u201313192. https:\/\/doi.org\/10.1021\/acscatal.2c03724.<\/p>\n<p>(216) Burlingham, S. J. ; Guijarro, D. ; Bosque, I. ; Chinchilla, R. ; Gonzalez-Gomez, J. C. (E)-alqu\u00e9nylation d\u00e9carboxylante m\u00e9di\u00e9e par la lumi\u00e8re visible d\u2019acides carboxyliques aliphatiques avec des aryl styryl sulfones dans des conditions sans m\u00e9tal. <em>Org. Biomol. Chem.<\/em> <strong>2022<\/strong>, <em>20<\/em> (40), 7923\u20137928. https:\/\/doi.org\/10.1039\/d2ob01360f.<\/p>\n<p>(217) Hardy, C. ; Kociok-K\u00f6hn, G. ; Buchard, A. D\u00e9gradation par les UV de mat\u00e9riaux en poly(acide lactique) par copolym\u00e9risation avec un xanthate cyclique d\u00e9riv\u00e9 du sucre. <em>Chem. Commun.<\/em> <strong>2022<\/strong>, <em>58<\/em> (36), 5463\u20135466. https:\/\/doi.org\/10.1039\/d2cc01322c.<\/p>\n<p>(218) Dasi, R. ; Villinger, A. ; Brasholz, M. Synth\u00e8se photocatalytique d\u2019az\u00e9tidine par cycloadditions [2 + 2] d\u00e9shydrog\u00e9nantes a\u00e9robies d\u2019amines avec des alc\u00e8nes. <em>Org. Lett.<\/em> <strong>2022<\/strong>, <em>24<\/em> (43), 8041\u20138046. https:\/\/doi.org\/10.1021\/acs.orglett.2c03291.<\/p>\n<p>(219) Jang, Y. J. ; An, H. ; Choi, S. ; Hong, J. ; Lee, H. Photocatalyse au Fe(III)(Btz)3 activ\u00e9e par la lumi\u00e8re verte dans une r\u00e9action de cycloaddition [4+2] cationique radicalaire. <em>Org. Lett.<\/em> <strong>2022<\/strong>, <em>24<\/em> (24), 4479\u20134484.<\/p>\n<p>(220) Lindsey Paul, Khuslen Enkhbold, Sydney Robinson, Than Thar Aye, Yuna Chung, Daniel P. Harrison, Julie A. Pollock, M. R. N. \u00c9lucidation du r\u00f4le des complexes [Ru(Bpy)2(OH2)2]2+ dans la chimioth\u00e9rapie photo-activ\u00e9e. <em>J. Inorg. Biochem.<\/em> <strong>2022<\/strong>, <em>235<\/em>.<\/p>\n<p>(221) Borlinghaus, N. ; Kaschel, J. ; Klee, J. ; Haller, V. ; Schetterl, J. ; Heitz, S. ; Lindner, T. ; Dietrich, J. D. ; Braje, W. M. ; Jolit, A. Capsules de r\u00e9actifs et de catalyseurs : un syst\u00e8me de distribution chimique pour le criblage de r\u00e9actions et la synth\u00e8se parall\u00e8le. <em>J. Org. Chem.<\/em> <strong>2021<\/strong>, <em>86<\/em>, 1357\u20131370. https:\/\/doi.org\/10.1021\/acs.joc.0c02576.<\/p>\n<p>(222) Kleinmans, R. ; Will, L. E. ; Schwarz, J. L. ; Glorius, F. 1,2-dialkylation d\u2019acrylates \u03b1-substitu\u00e9s activ\u00e9e par photoredox via un r\u00e9arrangement d\u2019Ireland\u2013Claisen. <em>Chem. Sci.<\/em> <strong>2021<\/strong>, <em>12<\/em>, 2816\u20132822. https:\/\/doi.org\/10.1039\/d0sc06385a.<\/p>\n<p>(223) Targos, K. ; Williams, O. P. ; Wickens, Z. K. R\u00e9v\u00e9lation du comportement de photo-oxydation puissant des photor\u00e9ducteurs catalytiques. <em>J. Am. Chem. Soc.<\/em> <strong>2021<\/strong>, 4125\u20134132. https:\/\/doi.org\/10.1021\/jacs.1c00399.<\/p>\n<p>(224) Bellottia, P. ; Koya, M. ; Gutheila, C. ; Heuvela, S. ; Glorius, F. Cascade de formation de trois liaisons \u00e0 trois composants via une catalyse photoredox au palladium. <em>Chem. Sci.<\/em> <strong>2021<\/strong>, <em>12<\/em> (1), 1810\u20131817. https:\/\/doi.org\/10.1021\/cen-v068n020.p042.<\/p>\n<p>(225) Crisenza, G. E. M. ; Faraone, A. ; Gandolfo, E. ; Mazzarella, D. ; Melchiorre, P. Couplages crois\u00e9s C\u2013C asym\u00e9triques catalytiques activ\u00e9s par photoexcitation. <em>Nat. Chem.<\/em> <strong>2021<\/strong>, <em>13<\/em> (6), 575\u2013580. https:\/\/doi.org\/10.1038\/s41557-021-00683-5.<\/p>\n<p>(226) Buglioni, L. ; Raymenants, F. ; Slattery, A. ; Zondag, S. D. A. ; Noel, T. Innovations technologiques en photochimie pour la synth\u00e8se organique : chimie en flux, exp\u00e9rimentation \u00e0 haut d\u00e9bit, mise \u00e0 l\u2019\u00e9chelle et photo\u00e9lectrochimie. <em>Chem. Rev.<\/em> <strong>2021<\/strong>. https:\/\/doi.org\/10.1021\/acs.chemrev.1c00332.<\/p>\n<p>(227) Watanabe, K. ; Terao, N. ; Niwa, T. ; Hosoya, T. 3-acylation directe d\u2019indolizines par des acides carboxyliques pour la synth\u00e8se pratique d\u2019acides carboxyliques prot\u00e9g\u00e9s lib\u00e9rables par la lumi\u00e8re rouge. <em>J. Org. Chem.<\/em> <strong>2021<\/strong>, <em>86<\/em> (17), 11822\u201311834. https:\/\/doi.org\/10.1021\/acs.joc.1c01244.<\/p>\n<p>(228) Zhao, B. ; Hammond, G. B. ; Xu, B. Synth\u00e8se photochimique de d\u00e9riv\u00e9s d\u2019imidazo-isoquinolinone catalys\u00e9e par une c\u00e9tone aromatique. <em>J. Org. Chem.<\/em> <strong>2021<\/strong>. https:\/\/doi.org\/10.1021\/acs.joc.1c01486.<\/p>\n<p>(229) Merkens, K. ; Jos\u00e9, F. ; Troyano, A. ; Anwar, K. ; G\u00f3mez-su\u00e1rez, A. Synth\u00e8se d\u2019acides \u03b3-oxo-\u03b1-amin\u00e9s via une acylation radicalaire avec des acides carboxyliques. <em>J. Org. Chem.<\/em> <strong>2021<\/strong>, <em>86<\/em> (12), 8448\u20138456. https:\/\/doi.org\/10.1021\/acs.joc.0c02951.<\/p>\n<p>(230) Zachmann, R. J. ; F\u00fcrstner, A. Hydrog\u00e9nation gem activ\u00e9e par la lumi\u00e8re : une entr\u00e9e orthogonale dans les catalyseurs au carb\u00e8ne de ruth\u00e9nium de \u00ab deuxi\u00e8me g\u00e9n\u00e9ration \u00bb pour la m\u00e9tath\u00e8se des ol\u00e9fines. <em>Chem. A Eurpean J.<\/em> <strong>2021<\/strong>, <em>27<\/em> (28), 7663\u20137666. https:\/\/doi.org\/10.1002\/chem.202101176.<\/p>\n<p>(231) Nugent, J. ; Sterling, A. J. ; Frank, N. ; Mousseau, J. J. ; Anderson, E. A. Synth\u00e8se de bicyclo[1.1.1]pentanes \u03b1-quaternaires par catalyse synergique organophotoredox et par transfert d\u2019atome d\u2019hydrog\u00e8ne. <em>Org. Lett.<\/em> <strong>2021<\/strong>, <em>23<\/em>, 8628\u20138633. https:\/\/doi.org\/10.1021\/acs.orglett.1c03346.<\/p>\n<p>(232) Askey, H. E. ; Grayson, J. D. ; Tibbetts, J. D. ; Turner-Dore, J. C. ; Holmes, J. M. ; Kociok-Kohn, G. ; Wrigley, G. L. ; Cresswell, A. J. Hydroaminoalkylation photocatalytique de styr\u00e8nes avec des alkylamines primaires non prot\u00e9g\u00e9es. <em>J. Am. Chem. Soc.<\/em> <strong>2021<\/strong>, <em>143<\/em> (39), 15936\u201315945. https:\/\/doi.org\/10.1021\/jacs.1c07401.<\/p>\n<p>(233) Varapragasam, S. J. P. ; Andriolo, J. M. ; Skinner, J. L. ; Grumstrup, E. M. R\u00e9duction photocatalytique de nitrates aqueux avec Ag\/g-C 3 N 4 hybride sous lumi\u00e8re ultraviolette et visible. <em>ACS Omega<\/em> <strong>2021<\/strong>. https:\/\/doi.org\/10.1021\/acsomega.1c05523.<\/p>\n<p>(234) Makino, K. ; Tozawa, K. ; Tanaka, Y. ; Inagaki, A. ; Tabata, H. ; Oshitari, T. ; Natsugari, H. ; Takahashi, H. Photorac\u00e9misation rapide de sulfoxydes d\u2019alkyle et d\u2019aryle chiraux. <em>J. Org. Chem.<\/em> <strong>2021<\/strong>, 1\u201350. https:\/\/doi.org\/10.1021\/acs.joc.1c02320.<\/p>\n<p>(235) Russo, C. ; Amato, J. ; Tron, G. C. ; Giustiniano, M. The Dark Side of Isocyanides: Visible-Light Photocatalytic Activity in the Oxidative Functionalization of C(Sp 3 )\u2013H Bonds. <em>J. Org. Chem.<\/em> <strong>2021<\/strong>, <em>86<\/em>, 18117\u201318127. https:\/\/doi.org\/10.1021\/acs.joc.1c02378.<\/p>\n<p>(236) Torregrosa-Chinillach, A. ; Chinchilla, R. Synthesis of Xanthones, Thioxanthones and Acridones by a Metal-Free Photocatalytic Oxidation Using Visible Light and Molecular Oxygen. <em>Molecules<\/em> <strong>2021<\/strong>, <em>26<\/em> (4). https:\/\/doi.org\/10.3390\/molecules26040974.<\/p>\n<p>(237) Borlinghaus, N. ; Sch\u00f6nfeld, B. ; Heitz, S. ; Klee, J. ; Vukeli\u0107, S. ; Braje, W. M. ; Jolit, A. Enabling Metallophotoredox Catalysis in Parallel Solution-Phase Synthesis Using Disintegrating Reagent Tablets. <em>J. Org. Chem.<\/em> <strong>2021<\/strong>, <em>86<\/em> (23), 16535\u201316547. https:\/\/doi.org\/10.1021\/acs.joc.1c01867.<\/p>\n<p>(238) Kerackian, T. ; Reina, A. ; Krachko, T. ; Boddaert, H. ; Bouyssi, D. ; Monteiro, N. ; Amgoune, A. C(Sp3)-H Bond Acylation with N -Acyl Imides under Photoredox\/ Nickel Dual Catalysis. <em>Synlett<\/em> <strong>2021<\/strong>, <em>32<\/em> (15), 1531\u20131536. https:\/\/doi.org\/10.1055\/s-0040-1707301.<\/p>\n<p>(239) Gomez Fernandez, M. A. ; Nascimento De Oliveira, M. ; Zanetti, A. ; Schwertz, G. ; Cossy, J. ; Amara, Z. Photochemical Hydrothiolation of Amorphadiene and Formal Synthesis of Artemisinin via a Pummerer Rearrangement. <em>Org. Lett.<\/em> <strong>2021<\/strong>, <em>23<\/em> (15), 5593\u20135598. https:\/\/doi.org\/10.1021\/acs.orglett.1c00636.<\/p>\n<p>(240) Trestsova, M. A. ; Utepova, I. A. ; Chupakhin, O. N. ; Semenov, M. V ; Pevtsov, D. N. ; Nikolenko, L. M. ; Tovstun, S. A. ; Gadomska, A. V ; Shchepochkin, A. V ; Kim, G. A. ; Razumov, V. F. ; Dorosheva, I. B. ; Rempel, A. A. Oxidative C-h\/c-h Coupling of Dipyrromethanes with Azines by TiO2-Based Photocatalytic System. Synthesis of New Bodipy Dyes and Their Photophysical and Electrochemical Properties. <em>Molecules<\/em> <strong>2021<\/strong>, <em>26<\/em> (18), 1\u201317. https:\/\/doi.org\/10.3390\/molecules26185549.<\/p>\n<p>(241) Komeyama, K. ; Michiyuki, T. ; Teshima, Y. ; Osaka, I. Visible Light-Driven Giese Reaction with Alkyl Tosylates Catalysed by Nucleophilic Cobalt. <em>RSC Adv.<\/em> <strong>2021<\/strong>, <em>11<\/em> (6), 3539\u20133546. https:\/\/doi.org\/10.1039\/d0ra10739e.<\/p>\n<p>(242) Graham, M. A. ; Noonan, G. ; Cherryman, J. H. ; Douglas, J. J. ; Gonzalez, M. ; Jackson, L. V. ; Leslie, K. ; Liu, Z. Q. ; McKinney, D. ; Munday, R. H. ; Parsons, C. D. ; Whittaker, D. T. E. ; Zhang, E. X. ; Zhang, J. W. Development and Proof of Concept for a Large-Scale Photoredox Additive-Free Minisci Reaction. <em>Org. Process Res. Dev.<\/em> <strong>2021<\/strong>, <em>25<\/em> (1), 57\u201367. https:\/\/doi.org\/10.1021\/acs.oprd.0c00483.<\/p>\n<p>(243) Sato, Y. ; Goto, Y. ; Nakamura, K. ; Miyamoto, Y. ; Sumida, Y. ; Ohmiya, H. Light-Driven N-Heterocyclic Carbene Catalysis Using Alkylborates. <em>ACS Catal.<\/em> <strong>2021<\/strong>, <em>11<\/em> (21), 12886\u201312892. https:\/\/doi.org\/10.1021\/acscatal.1c04153.<\/p>\n<p>(244) Patra, T. ; Das, M. ; Daniliuc, C. G. ; Glorius, F. Metal-Free Photosensitized Oxyimination of Unactivated Alkenes with Bifunctional Oxime Carbonates. <em>Nat. Catal.<\/em> <strong>2021<\/strong>, <em>4<\/em> (1), 54\u201361. https:\/\/doi.org\/10.1038\/s41929-020-00553-2.<\/p>\n<p>(245) Ma, J. ; Chen, S. ; Bellotti, P. ; Guo, R. ; Sch\u00e4fer, F. ; Heusler, A. ; Zhang, X. ; Daniliuc, C. ; Brown, M. K. ; Houk, K. N. ; Glorius, F. Photochemical Intermolecular Dearomative Cycloaddition of Bicyclic Azaarenes with Alkenes. <em>Science (80-. ).<\/em> <strong>2021<\/strong>, <em>371<\/em> (6536), 1338\u20131345. https:\/\/doi.org\/10.1126\/science.abg0720.<\/p>\n<p>(246) Huang, H. M. ; Bellotti, P. ; Daniliuc, C. G. ; Glorius, F. Radical Carbonyl Propargylation by Dual Catalysis. <em>Angew. Chemie &#8211; Int. Ed.<\/em> <strong>2021<\/strong>, <em>60<\/em> (5), 2464\u20132471. https:\/\/doi.org\/10.1002\/anie.202011996.<\/p>\n<p>(247) Liang, Y. ; Strieth-Kalthoff, F. ; Bellotti, P. ; Glorius, F. Catalytic One-Carbon Homologation of \u03b1-Amino Acids to \u03b2-Amino Aldehydes. <em>Chem Catal.<\/em> <strong>2021<\/strong>, <em>1<\/em> (7), 1427\u20131436. https:\/\/doi.org\/10.1016\/j.checat.2021.10.010.<\/p>\n<p>(248) Alfonzo, E. ; Hande, S. M. \u03b1\u2013Heteroarylation of Thioethers via Photoredox and Weak Br\u00f8nsted Base Catalysis. <em>Org. Lett.<\/em> <strong>2021<\/strong>, <em>23<\/em> (15), 6115\u20136120.<\/p>\n<p>(249) Hell, S. M. ; Meyer, C. F. ; Ortalli, S. ; Sap, J. B. I. ; Chen, X. ; Gouverneur, V. Hydrofluoromethylation of Alkenes with Fluoroiodomethane and Beyond. <em>Chem. Sci.<\/em> <strong>2021<\/strong>, <em>12<\/em> (36), 12149\u201312155. https:\/\/doi.org\/10.1039\/d1sc03421a.<\/p>\n<p>(250) Delgado, P. ; Glass, R. J. ; Geraci, G. ; Duvadie, R. ; Majumdar, D. ; Robinson, R. I. ; Elmaarouf, I. ; Mikus, M. ; Tan, K. L. Use of Green Solvents in Metallaphotoredox Cross-Electrophile Coupling Reactions Utilizing a Lipophilic Modified Dual Ir\/Ni Catalyst System. <em>J. Org. Chem.<\/em> <strong>2021<\/strong>, <em>86<\/em> (23), 17428\u201317436. https:\/\/doi.org\/10.1021\/acs.joc.1c02013.<\/p>\n<p>(251) Fernandez-Rodriguez, P. ; Legros, F. ; Maier, T. ; Weber, A. ; M\u00e9ndez, M. ; Derdau, V. ; Hessler, G. ; Kurz, M. ; Villar-Garea, A. ; Ruf, S. Photoinduced Decarboxylative Radical Addition Reactions for Late Stage Functionalization of Peptide Substrates. <em>European J. Org. Chem.<\/em> <strong>2021<\/strong>, No. 5, 782\u2013787. https:\/\/doi.org\/10.1093\/ejo\/cjy009.<\/p>\n<p>(252) John, A. ; Paul, A. ; Leitch, J. A. ; Yamazaki, K. ; Christensen, K. E. ; Cassar, D. J. ; Hamlin, T. A. ; Dixon, D. J. Switchable, Reagent-Controlled Diastereodivergent Photocatalytic Carbocyclisation of Imine-Derived \u03b1-Amino Radicals. <em>Angew. Chem. Int. Ed.<\/em> <strong>2021<\/strong>, <em>60<\/em> (45), 24116\u201324123. https:\/\/doi.org\/10.1002\/anie.202107253.<\/p>\n<p>(253) D., S. T. ; Chatterjee, A. ; Schekin, D. ; Wagner, T. ; Zach, J. ; Johansson, M. J. ; Bergonzini, G. ; K\u00f6nig, B. ; Svejstrup, T. D. ; Chatterjee, A. ; Schekin, D. ; Wagner, T. ; Zach, J. ; Johansson, M. J. ; Bergonzini, G. ; K\u00f6nig, B. Effects of Light Intensity and Reaction Temperature on Photoreactions in Commercial Photoreactors. <em>ChemPhotoChem<\/em> <strong>2021<\/strong>, <em>5<\/em> (9), 808\u2013814. https:\/\/doi.org\/10.1007\/978-88-7642-577-6_6.<\/p>\n<p>(254) Jia, X. ; Zhang, Z. ; Gevorgyan, V. Three-Component Visible Light-Induced Palladium Catalyzed 1,2- Alkyl Carbamoylation\/Cyanation of Alkenes. <em>ACS Catal.<\/em> <strong>2021<\/strong>, <em>11<\/em> (21), 13217\u201313222.<\/p>\n<p>(255) Wang, H. ; Bellotti, P. ; Zhang, X. ; Paulisch, T. O. ; Glorius, F. A Base-Controlled Switch of SO2 Reincorporation in Photocatalyzed Radical Difunctionalization of Alkenes. <em>Chem<\/em> <strong>2021<\/strong>, <em>7<\/em> (12), 3412\u20133424. https:\/\/doi.org\/10.1016\/j.chempr.2021.10.007.<\/p>\n<p>(256) Andrews, J. A. ; Pantaine, L. R. E. ; Palmer, C. F. ; Poole, D. L. ; Willis, M. C. Sulfinates from Amines: A Radical Approach to Alkyl Sulfonyl Derivatives via Donor-Acceptor Activation of Pyridinium Salts. <em>Org. Lett.<\/em> <strong>2021<\/strong>, <em>23<\/em> (21), 8488\u20138493. https:\/\/doi.org\/10.1021\/acs.orglett.1c03194.<\/p>\n<p>(257) Russo, C. ; Cannalire, R. ; Luciano, P. ; Brunelli, F. ; Tron, G. C. ; Giustiniano, M. Visible-Light Photocatalytic Ugi\/Aza-Wittig Cascade towards 2-Aminomethyl-1,3,4-Oxadiazole Derivatives. <em>Synthesis (Stuttg).<\/em> <strong>2021<\/strong>, <em>53<\/em> (23), 4419\u20134427.<\/p>\n<p>(258) Dutysheva, E. A. ; Utepova, I. A. ; Trestsova, M. A. ; Charushin, A. S. A. V. N. ; Chupakhin, O. N. ; Margulis, B. A. ; Guzhova, I. V. ; Lazarev, V. F. Synthesis and Approbation of New Neuroprotective Chemicals of Pyrrolyl- and Indolylazine Classes in a Cell Model of Alzheimer\u2019s Disease. <em>Eur. J. Med. Chem.<\/em> <strong>2021<\/strong>, <em>222<\/em>, 113577.<\/p>\n<p>(259) Seefeldt, P. ; Dasi, R. ; Villinger, A. ; Brasholz, M. Photoredox-Induced Deaminative Radical-Cationic Three-Component Couplings with N-Alkylpyridinium Salts and Alkenes. <em>ChemPhotoChem<\/em> <strong>2021<\/strong>, <em>5<\/em> (11), 979\u2013983. https:\/\/doi.org\/10.1002\/cptc.202100226.<\/p>\n<p>(260) P\u00e9ault, L. ; Planchat, A. ; Nun, P. ; Le Grognec, E. ; Coeffard, V. Atom Economical Photocatalytic Oxidation of Phenols and Site-Selective Epoxidation Toward Epoxyquinols. <em>J. Org. Chem.<\/em> <strong>2021<\/strong>, <em>86<\/em> (24), 18192\u201318203. https:\/\/doi.org\/10.1021\/acs.joc.1c02459.<\/p>\n<p>(261) Takeda, D. ; Yoritate, M. ; Yasutomi, H. ; Chiba, S. ; Yokoo, A. ; Usui, K. ; Hirai, G. \u03b2-Glycosyl Trifluoroborates as Precursors for Direct \u03b1- C -Glycosylation : Synthesis of 2-Deoxy-\u03b1- C -Glycosides. <em>Org. Lett.<\/em> <strong>2021<\/strong>, <em>23<\/em>, 1940\u20131944.<\/p>\n<p>(262) Greener, A. J. ; Ubysz, P. ; Owens-Ward, W. ; Smith, G. ; Oca\u00f1a, I. ; Whitwood, A. C. ; Chechik, V. ; James, M. J. Radical-Anion Coupling through Reagent Design: Hydroxylation of Aryl Halides. <em>Chem. Sci.<\/em> <strong>2021<\/strong>, <em>12<\/em> (43), 14641\u201314646. https:\/\/doi.org\/10.1039\/d1sc04748e.<\/p>\n<p>(263) Leitch, J. A. ; Rogova, T. ; Duarte, F. ; Dixon, D. J. Dearomative Photocatalytic Construction of Bridged 1,3-Diazepanes. <em>Angew. Chemie &#8211; Int. Ed.<\/em> <strong>2020<\/strong>, <em>59<\/em> (10), 4121\u20134130. https:\/\/doi.org\/10.1002\/anie.201914390.<\/p>\n<p>(264) Cannalire, R. ; Amato, J. ; Summa, V. ; Novellino, E. ; Tron, G. C. ; Giustiniano, M. Visible-Light Photocatalytic Functionalization of Isocyanides for the Synthesis of Secondary Amides and Ketene Aminals. <em>J. Org. Chem.<\/em> <strong>2020<\/strong>, <em>85<\/em> (21), 14077\u201314086. https:\/\/doi.org\/10.1021\/acs.joc.0c01946.<\/p>\n<p>(265) Nehme, S. I. ; Crocker, L. ; Fruk, L. Flavin-Conjugated Iron Oxide Nanoparticles as Enyzme-Inspired Photocatalysts for Azo Dye Degradation. <em>Catalysts<\/em> <strong>2020<\/strong>, <em>10<\/em> (324), 1\u201318.<\/p>\n<p>(266) Kerackian, T. ; Reina, A. ; Bouyssi, D. ; Monteiro, N. ; Amgoune, A. Silyl Radical Mediated Cross-Electrophile Coupling of N-Acyl-Imides with Alkyl Bromides under Photoredox\/Nickel Dual Catalysis. <em>Org. Lett.<\/em> <strong>2020<\/strong>, <em>22<\/em> (6), 2240\u20132245.<\/p>\n<p>(267) Gueret, R. ; Pelinski, L. ; Bousquet, T. ; Sauthier, M. ; Ferey, V. ; Bigot, A. Visible-Light-Driven CarboxyLic Amine Protocol (CLAP) for the Synthesis of 2-Substituted Piperazines under Batch and Flow Conditions. <em>Org. Lett.<\/em> <strong>2020<\/strong>, <em>22<\/em> (13), 5157\u20135162. https:\/\/doi.org\/10.1021\/acs.orglett.0c01759.<\/p>\n<p>(268) Patra, T. ; Bellotti, P. ; Strieth-Kalthoff, F. ; Glorius, F. Photosensitized Intermolecular Carboimination of Alkenes through the Persistent Radical Effect. <em>Angew. Chemie &#8211; Int. Ed.<\/em> <strong>2020<\/strong>, <em>59<\/em> (8), 3172\u20133177. https:\/\/doi.org\/10.1002\/anie.201912907.<\/p>\n<p>(269) Angnes, R. A. ; Potnis, C. ; Liang, S. ; Correia, C. R. D. ; Hammond, G. B. Photoredox-Catalyzed Synthesis of Alkylaryldiazenes: Formal Deformylative C-N Bond Formation with Alkyl Radicals. <em>J. Org. Chem.<\/em> <strong>2020<\/strong>, <em>85<\/em> (6), 4153\u20134164. https:\/\/doi.org\/10.1021\/acs.joc.9b03341.<\/p>\n<p>(270) Grimm, I. ; Hauer, S. T. ; Schulte, T. ; Wycich, G. ; Collins, K. D. ; Lovis, K. ; Candish, L. Upscaling Photoredox Cross-Coupling Reactions in Batch Using Immersion-Well Reactors. <em>Org. Process Res. Dev.<\/em> <strong>2020<\/strong>, <em>24<\/em> (6), 1185\u20131193. https:\/\/doi.org\/10.1021\/acs.oprd.0c00070.<\/p>\n<p>(271) Ryder, A. S. H. ; Cunningham, W. B. ; Ballantyne, G. ; Mules, T. ; Kinsella, A. G. ; Turner-Dore, J. ; Alder, C. M. ; Edwards, L. J. ; McKay, B. S. J. ; Grayson, M. N. ; Cresswell, A. J. Photocatalytic \u03b1-Tertiary Amine Synthesis via C\u2212H Alkylation of Unmasked Primary Amines. <em>Angew. Chemie &#8211; Int. Ed.<\/em> <strong>2020<\/strong>, <em>59<\/em> (35), 14986\u201314991. https:\/\/doi.org\/10.1002\/anie.202005294.<\/p>\n<p>(272) Beato, E. D. P. ; Mazzarella, D. ; Balletti, M. ; Melchiorre, P. Photochemical Generation of Acyl and Carbamoyl Radicals Using a Nucleophilic Organic Catalyst: Applications and Mechanism Thereof. <em>Chem. Sci.<\/em> <strong>2020<\/strong>, <em>11<\/em> (24), 6312\u20136324. https:\/\/doi.org\/10.1039\/d0sc02313b.<\/p>\n<p>(273) Alfonzo, E. ; Hande, S. M. Photoredox and Weak Br\u00f8nsted Base Dual Catalysis: Alkylation of \u03b1-Thio Alkyl Radicals. <em>ACS Catal.<\/em> <strong>2020<\/strong>, <em>10<\/em> (21), 12590\u201312595. https:\/\/doi.org\/10.1021\/acscatal.0c03851.<\/p>\n<p>(274) Sch\u00e4fers, F. ; Quach, L. ; Luca Schwarz, J. ; Saladrigas, M. ; Daniliuc, C. G. ; Glorius, F. Direct Access to Mono-Protected Homoallylic 1,2-Diols via Dual Chromium\/ Photoredox Catalysis. <em>ACS Catal.<\/em> <strong>2020<\/strong>, 1\u201389. https:\/\/doi.org\/10.26434\/CHEMRXIV.12670901.V1.<\/p>\n<p>(275) Shea, M. D. ; Mansoor, U. F. ; Hopkins, B. A. A Metallaphotoredox Method for the Expansion of Benzyl SAR on Electron-Deficient Amines. <em>Org. Lett.<\/em> <strong>2020<\/strong>, <em>22<\/em> (3), 1052\u20131055. https:\/\/doi.org\/10.1021\/acs.orglett.9b04587.<\/p>\n<p>(276) Takeuchi, H. ; Inuki, S. ; Nakagawa, K. ; Kawabe, T. ; Ichimura, A. ; Oishi, S. ; Ohno, H. Total Synthesis of Zephycarinatines via Photocatalytic Reductive Radical Ipso \u2010Cyclization. <em>Angew. Chemie<\/em> <strong>2020<\/strong>, <em>59<\/em> (16), 21210\u201321215. https:\/\/doi.org\/10.1002\/ange.202009399.<\/p>\n<p>(277) Pelliccia, S. ; Alfano, A. I. ; Luciano, P. ; Novellino, E. ; Massarotti, A. ; Tron, G. C. ; Ravelli, D. ; Giustiniano, M. Photocatalytic Isocyanide-Based Multicomponent Domino Cascade Towards the Stereoselective Formation of Iminofurans. <em>J. Org. Chem.<\/em> <strong>2020<\/strong>, <em>85<\/em> (4), 1981\u20131990. https:\/\/doi.org\/https:\/\/doi.org\/10.1021\/acs.joc.9b02709.<\/p>\n<p>(278) Buss, B. L. ; Lim, C. H. ; Miyake, G. M. Dimethyl Dihydroacridines as Photocatalysts in Organocatalyzed Atom Transfer Radical Polymerization of Acrylate Monomers. <em>Angew. Chemie &#8211; Int. Ed.<\/em> <strong>2020<\/strong>, <em>59<\/em> (8), 3209\u20133217. https:\/\/doi.org\/10.1002\/anie.201910828.<\/p>\n<p>(279) Barday, M. ; Blieck, R. ; Ruyet, L. ; Besset, T. Remote Trifluoromethylthiolation of Alcohols under Visible Light. <em>Tetrahedron<\/em> <strong>2020<\/strong>, <em>76<\/em> (51), 131153. https:\/\/doi.org\/10.1016\/j.tet.2020.131153.<\/p>\n<p>(280) Sandfort, F. ; Knecht, T. ; Pinkert, T. ; Daniliuc, C. G. ; Glorius, F. Site-Selective Thiolation of (Multi)Halogenated Heteroarenes. <em>J. Am. Chem. Soc<\/em> <strong>2020<\/strong>, <em>142<\/em> (15), 6913\u20136919.<\/p>\n<p>(281) Schwarz, J. L. ; Kleinmans, R. ; Paulisch, T. O. ; Glorius, F. 1,2-Aminoalcohols via Cr \/ Photoredox Dual Catalyzed Addition of \u03b1-Aminocarbanion Equivalents to Carbonyls. <em>J. Am. Chem. Soc<\/em> <strong>2020<\/strong>, <em>142<\/em> (5), 2168\u20132174.<\/p>\n<p>(282) Schwarz, J. L. ; Huang, H. M. ; Paulisch, T. O. ; Glorius, F. Dialkylation of 1,3-Dienes by Dual Photoredox and Chromium Catalysis. <em>ACS Catal.<\/em> <strong>2020<\/strong>, <em>10<\/em> (2), 1621\u20131627. https:\/\/doi.org\/10.1021\/acscatal.9b04222.<\/p>\n<p>(283) Merkens, K. ; Aguilar Troyano, F. J. ; Djossou, J. ; G\u00f3mez-Su\u00e1rez, A. Synthesis of Unnatural \u03b1-Amino Acid Derivatives via Light-Mediated Radical Decarboxylative Processes. <em>Adv. Synth. Catal.<\/em> <strong>2020<\/strong>, <em>362<\/em> (12), 2354\u20132359. https:\/\/doi.org\/10.1002\/adsc.202000300.<\/p>\n<p>(284) Rogova, T. ; Gabriel, P. ; Zavitsanou, S. ; Leitch, J. A. ; Duarte, F. ; Dixon, D. J. Reverse Polarity Reductive Functionalization of Tertiary Amides via a Dual Iridium-Catalyzed Hydrosilylation and Single Electron Transfer Strategy. <em>ACS Catal.<\/em> <strong>2020<\/strong>, <em>10<\/em> (19), 11438\u201311447. https:\/\/doi.org\/10.1021\/acscatal.0c03089.<\/p>\n<p>(285) Leitch, J. A. ; Rossolini, T. ; Rogova, T. ; Dixon, D. J. \u03b1-Tertiary Dialkyl Ether Synthesis via Reductive Photocatalytic \u03b1-Functionalization of Alkyl Enol Ethers. <em>ACS Catal.<\/em> <strong>2020<\/strong>, <em>10<\/em> (19), 11430\u201311437. https:\/\/doi.org\/10.1021\/acscatal.0c02584.<\/p>\n<p>(286) Ramirez, N. P. ; Lana-Villarreal, T. ; Gonzalez-Gomez, J. C. Direct Decarboxylative Allylation and Arylation of Aliphatic Carboxylic Acids Using Flavin-Mediated Photoredox Catalysis. <em>European J. Org. Chem.<\/em> <strong>2020<\/strong>, <em>2020<\/em> (10), 1539\u20131550. https:\/\/doi.org\/10.1002\/ejoc.201900888.<\/p>\n<p>(287) Escobar, R. A. ; Johannes, J. W. A Unified and Practical Method for Carbon\u2013Heteroatom Cross-Coupling Using Nickel\/Photo Dual Catalysis. <em>Chem. &#8211; A Eur. J.<\/em> <strong>2020<\/strong>, <em>26<\/em> (23), 5168\u20135173.<\/p>\n<p>(288) Cardinale, L. ; Konev, M. O. ; Jacobi Von Wangelin, A. Photoredox-Catalyzed Addition of Carbamoyl Radicals to Olefins: A 1,4-Dihydropyridine Approach. <em>Chem. Eur. J.<\/em> <strong>2020<\/strong>, <em>26<\/em> (37), 8239\u20138243.<\/p>\n<p>(289) Legros, F. ; Fernandez-Rodriguez, P. ; Mishra, A. ; Weck, R. ; Bauer, A. ; Sandvoss, M. ; Ruf, S. ; Mendez, M. ; Mora-Rado, H. ; Rackelmann, N. ; Poverlein, C. ; Derdau, V. Photoredox-Mediated Hydrogen Isotope Exchange Reactions of Amino-Acids, Peptides, and Peptide-Derived Drugs. <em>Chem. Eur. J.<\/em> <strong>2020<\/strong>, <em>26<\/em> (56), 12738\u201312742.<\/p>\n<p>(290) Lyu, J. ; Claraz, A. ; Vitale, M. R. ; Allain, C. ; Masson, G. Preparation of Chiral Photosensitive Organocatalysts and Their Application for the Enantioselective Synthesis of 1,2-Diamines. <em>J. Org. Chem.<\/em> <strong>2020<\/strong>, <em>85<\/em> (20), 12843\u201312855. https:\/\/doi.org\/10.1021\/acs.joc.0c01931.<\/p>\n<p>(291) Gallhof, M. ; Kell, L. ; Brasholz, M. Ligand Substitution of RuII\u2013Alkylidenes to Ru(Bpy)32+: Sequential Olefin Metathesis\/Photoredox Catalysis. <em>Chem. &#8211; A Eur. J.<\/em> <strong>2020<\/strong>, <em>26<\/em> (8), 1772\u20131775. https:\/\/doi.org\/10.1002\/chem.201905694.<\/p>\n<p>(292) Aguilar Troyano, F. J. ; Ballaschk, F. ; Jaschinski, M. ; \u00d6zkaya, Y. ; G\u00f3mez-Su\u00e1rez, A. Light-Mediated Formal Radical Deoxyfluorination of Tertiary Alcohols through Selective Single-Electron Oxidation with TEDA2+. <em>Chem. &#8211; A Eur. J.<\/em> <strong>2019<\/strong>, <em>25<\/em> (62), 14054\u201314058. https:\/\/doi.org\/10.1002\/chem.201903702.<\/p>\n<p>(293) Grainger, R. ; Heightman, T. D. ; Ley, S. V. ; Lima, F. ; Johnson, C. N. Enabling Synthesis in Fragment-Based Drug Discovery by Reactivity Mapping: Photoredox-Mediated Cross-Dehydrogenative Heteroarylation of Cyclic Amines. <em>Chem. Sci.<\/em> <strong>2019<\/strong>, <em>10<\/em> (8), 2264\u20132271. https:\/\/doi.org\/10.1039\/C8SC04789H.<\/p>\n<p>(294) Bieszczad, B. ; Perego, L. A. ; Melchiorre, P. Photochemical C\u2212H Hydroxyalkylation of Quinolines and Isoquinolines. <em>Angew. Chemie &#8211; Int. Ed.<\/em> <strong>2019<\/strong>, <em>58<\/em> (47), 16878\u201316883. https:\/\/doi.org\/10.1002\/anie.201910641.<\/p>\n<p>(295) Nugent, J. ; Arroniz, C. ; Shire, B. R. ; Sterling, A. J. ; Pickford, H. D. ; Wong, M. L. J. ; Mansfield, S. J. ; Caputo, D. F. J. ; Owen, B. ; Mousseau, J. J. ; Duarte, F. ; Anderson, E. A. A General Route to Bicyclo[1.1.1]Pentanes through Photoredox Catalysis. <em>ACS Catal.<\/em> <strong>2019<\/strong>, <em>9<\/em> (10), 9568\u20139574. https:\/\/doi.org\/10.1021\/acscatal.9b03190.<\/p>\n<p>(296) Meyer, C. F. ; Hell, S. M. ; Misale, A. ; Trabanco, A. A. ; Gouverneur, V. Hydrodifluoromethylation of Alkenes with Difluoroacetic Acid. <em>Angew. Chemie &#8211; Int. Ed.<\/em> <strong>2019<\/strong>, <em>58<\/em> (26), 8829\u20138833. https:\/\/doi.org\/10.1002\/anie.201903801.<\/p>\n<p>(297) Rossolini, T. ; Ferko, B. ; Dixon, D. J. Photocatalytic Reductive Formation of \u03b1-Tertiary Ethers from Ketals. <em>Org. Lett.<\/em> <strong>2019<\/strong>, <em>21<\/em> (17), 6668\u20136673. https:\/\/doi.org\/10.1021\/acs.orglett.9b02273.<\/p>\n<p>(298) Ramirez, N. P. ; K\u00f6nig, B. ; Gonzalez-Gomez, J. C. Decarboxylative Cyanation of Aliphatic Carboxylic Acids via Visible-Light Flavin Photocatalysis. <em>Org. Lett.<\/em> <strong>2019<\/strong>, <em>21<\/em> (5), 1368\u20131373.<\/p>\n<p>(299) Fischer, F. ; Hapke, M. Air-Stable CpCoI\u2013Phosphite\u2013Fumarate Precatalyst in Cyclization Reactions: Comparing Different Methods of Energy Supply. <em>European J. Org. Chem.<\/em> <strong>2018<\/strong>, <em>2018<\/em> (24), 3193\u20133201. https:\/\/doi.org\/10.1002\/ejoc.201800196.<\/p>\n<p>(300) Hsieh, H.-W. ; Coley, C. W. ; Baumgartner, L. M. ; Jensen, K. F. ; Richard, I. ; Robinson, R. I. Photoredox Iridium\u2013Nickel Dual-Catalyzed Decarboxylative Arylation Cross-Coupling: From Batch to Continuous Flow via Self-Optimizing Segmented Flow Reactor. <em>Org. Process Res. Dev.<\/em> <strong>2018<\/strong>, acs.oprd.8b00018. https:\/\/doi.org\/10.1021\/acs.oprd.8b00018.<\/p>\n<p>(301) Su, J. Y. ; Gr\u00fcnenfelder, D. C. ; Takeuchi, K. ; Reisman, S. E. Radical Deoxychlorination of Cesium Oxalates for the Synthesis of Alkyl Chlorides. <em>Org. Lett.<\/em> <strong>2018<\/strong>, <em>20<\/em> (16), 4912\u20134916. https:\/\/doi.org\/10.1021\/acs.orglett.8b02045.<\/p>\n<p>(302) Leitch, J. A. ; Fuentes De Arriba, A. L. ; Tan, J. ; Hoff, O. ; Mart\u00ednez, C. M. ; Dixon, D. J. Photocatalytic Reverse Polarity Povarov Reaction. <em>Chem. Sci.<\/em> <strong>2018<\/strong>, <em>9<\/em> (32), 6653\u20136658. https:\/\/doi.org\/10.1039\/c8sc01704b.<\/p>\n<p>(303) Davies, J. ; Angelini, L. ; Alkhalifah, M. A. ; Sanz, L. M. ; Sheikh, N. S. ; Leonori, D. Photoredox Synthesis of Arylhydroxylamines from Carboxylic Acids and Nitrosoarenes. <em>Synth.<\/em> <strong>2018<\/strong>, <em>50<\/em> (4), 821\u2013830. https:\/\/doi.org\/10.1055\/s-003.<\/p>\n<p>(304) L\u00e4mmermann, H. ; Sudau, A. ; Rackl, D. ; Weinmann, H. ; Collins, K. ; Wortmann, L. ; Candish, L. ; Hog, D. T. ; Meier, R. Late-Stage Sulfoximidation of Electron-Rich Arenes by Photoredox Catalysis. <em>Synlett<\/em> <strong>2018<\/strong>, <em>29<\/em> (20), 2679\u20132684. https:\/\/doi.org\/10.1055\/s-003.<\/p>\n<p>(305) Rossolini, T. ; Leitch, J. A. ; Grainger, R. ; Dixon, D. J. Photocatalytic Three-Component Umpolung Synthesis of 1,3-Diamines. <em>Org. Lett.<\/em> <strong>2018<\/strong>, <em>20<\/em> (21), 6794\u20136798. https:\/\/doi.org\/10.1021\/acs.orglett.8b02923.<\/p>\n<p>(306) Morcillo, S. P. ; Dauncey, E. M. ; Kim, J. H. ; Douglas, J. J. ; Sheikh, N. S. ; Leonori, D. Photoinduced Remote Functionalization of Amides and Amines Using Electrophilic Nitrogen Radicals. <em>Angew. Chemie &#8211; Int. Ed.<\/em> <strong>2018<\/strong>, <em>57<\/em> (39), 12945\u201312949. https:\/\/doi.org\/10.1002\/anie.201807941.<\/p>\n<p>(307) Konev, M. O. ; McTeague, T. A. ; Johannes, J. W. Nickel-Catalyzed Photoredox-Mediated Cross-Coupling of Aryl Electrophiles and Aryl Azides. <em>ACS Catal.<\/em> <strong>2018<\/strong>, <em>8<\/em> (10), 9120\u20139124. https:\/\/doi.org\/10.1021\/acscatal.8b02954.<\/p>\n<p>(308) Vil\u00e9, G. ; Richard-Bildstein, S. ; Lhuillery, A. ; Rueedi, G. Electrophile, Substrate Functionality, and Catalyst Effects in the Synthesis of \u03b1-Mono and Di-Substituted Benzylamines via Visible-Light Photoredox Catalysis in Flow. <em>ChemCatChem<\/em> <strong>2018<\/strong>, <em>10<\/em> (17), 3786\u20133794. https:\/\/doi.org\/10.1002\/cctc.201800754.<\/p>\n<p>[\/et_pb_text][\/et_pb_column][\/et_pb_row][\/et_pb_section]<\/p>\n","protected":false},"excerpt":{"rendered":"<p>La PhotoRedOx Box&#x2122; d\u2019EvoluChem est le photor\u00e9acteur de photochimie de choix pour le chimiste qui cherche \u00e0 standardiser les installations photochimiques de laboratoire de mani\u00e8re \u00e9conomique. Sa conception flexible permet l\u2019utilisation de LED interchangeables de 365 nm \u00e0 808 nm et d\u2019une grande vari\u00e9t\u00e9 de flacons. Ce photor\u00e9acteur de photochimie (brevet am\u00e9ricain n\u00b0 10\u202f906\u202f022) est [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":23975,"parent":23917,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_et_pb_use_builder":"on","_et_pb_old_content":"","_et_gb_content_width":"","footnotes":""},"class_list":["post-23974","page","type-page","status-publish","has-post-thumbnail","hentry"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.7 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>PhotoRedOx Box\u2122 | Photor\u00e9acteur PhotoRedox par HepatoChem<\/title>\n<meta name=\"description\" content=\"D\u00e9couvrez le photor\u00e9acteur PhotoRedox d\u2019HepatoChem. C\u2019est la solution id\u00e9ale pour toute installation de photochimie en laboratoire.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/hepatochem.com\/fr\/photoreacteurs-accessoires-led-et-plus-encore\/photoredox-box\/\" \/>\n<meta name=\"twitter:label1\" content=\"Dur\u00e9e de lecture estim\u00e9e\" \/>\n\t<meta name=\"twitter:data1\" content=\"71 minutes\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\\\/\\\/schema.org\",\"@graph\":[{\"@type\":\"WebPage\",\"@id\":\"https:\\\/\\\/hepatochem.com\\\/fr\\\/photoreacteurs-accessoires-led-et-plus-encore\\\/photoredox-box\\\/\",\"url\":\"https:\\\/\\\/hepatochem.com\\\/fr\\\/photoreacteurs-accessoires-led-et-plus-encore\\\/photoredox-box\\\/\",\"name\":\"PhotoRedOx Box\u2122 | Photor\u00e9acteur PhotoRedox par HepatoChem\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/hepatochem.com\\\/fr\\\/#website\"},\"primaryImageOfPage\":{\"@id\":\"https:\\\/\\\/hepatochem.com\\\/fr\\\/photoreacteurs-accessoires-led-et-plus-encore\\\/photoredox-box\\\/#primaryimage\"},\"image\":{\"@id\":\"https:\\\/\\\/hepatochem.com\\\/fr\\\/photoreacteurs-accessoires-led-et-plus-encore\\\/photoredox-box\\\/#primaryimage\"},\"thumbnailUrl\":\"https:\\\/\\\/hepatochem.com\\\/wp-content\\\/uploads\\\/2023\\\/09\\\/PhotoRedOx-Box-on-blend-9.27.23-1-e1695835529712.jpg\",\"datePublished\":\"2022-08-06T19:39:48+00:00\",\"dateModified\":\"2026-06-02T12:00:05+00:00\",\"description\":\"D\u00e9couvrez le photor\u00e9acteur PhotoRedox d\u2019HepatoChem. C\u2019est la solution id\u00e9ale pour toute installation de photochimie en laboratoire.\",\"breadcrumb\":{\"@id\":\"https:\\\/\\\/hepatochem.com\\\/fr\\\/photoreacteurs-accessoires-led-et-plus-encore\\\/photoredox-box\\\/#breadcrumb\"},\"inLanguage\":\"fr-FR\",\"potentialAction\":[{\"@type\":\"ReadAction\",\"target\":[\"https:\\\/\\\/hepatochem.com\\\/fr\\\/photoreacteurs-accessoires-led-et-plus-encore\\\/photoredox-box\\\/\"]}]},{\"@type\":\"ImageObject\",\"inLanguage\":\"fr-FR\",\"@id\":\"https:\\\/\\\/hepatochem.com\\\/fr\\\/photoreacteurs-accessoires-led-et-plus-encore\\\/photoredox-box\\\/#primaryimage\",\"url\":\"https:\\\/\\\/hepatochem.com\\\/wp-content\\\/uploads\\\/2023\\\/09\\\/PhotoRedOx-Box-on-blend-9.27.23-1-e1695835529712.jpg\",\"contentUrl\":\"https:\\\/\\\/hepatochem.com\\\/wp-content\\\/uploads\\\/2023\\\/09\\\/PhotoRedOx-Box-on-blend-9.27.23-1-e1695835529712.jpg\",\"width\":1370,\"height\":1080,\"caption\":\"A blue box with a cup on top of it.\"},{\"@type\":\"BreadcrumbList\",\"@id\":\"https:\\\/\\\/hepatochem.com\\\/fr\\\/photoreacteurs-accessoires-led-et-plus-encore\\\/photoredox-box\\\/#breadcrumb\",\"itemListElement\":[{\"@type\":\"ListItem\",\"position\":1,\"name\":\"Photor\u00e9acteurs, accessoires, LED et plus encore\",\"item\":\"https:\\\/\\\/hepatochem.com\\\/fr\\\/photoreacteurs-accessoires-led-et-plus-encore\\\/\"},{\"@type\":\"ListItem\",\"position\":2,\"name\":\"PhotoRedOx Box&#x2122;\"}]},{\"@type\":\"WebSite\",\"@id\":\"https:\\\/\\\/hepatochem.com\\\/fr\\\/#website\",\"url\":\"https:\\\/\\\/hepatochem.com\\\/fr\\\/\",\"name\":\"HepatoChem\",\"description\":\"Reinventing Chemistry for Life Sciences\",\"publisher\":{\"@id\":\"https:\\\/\\\/hepatochem.com\\\/fr\\\/#organization\"},\"potentialAction\":[{\"@type\":\"SearchAction\",\"target\":{\"@type\":\"EntryPoint\",\"urlTemplate\":\"https:\\\/\\\/hepatochem.com\\\/fr\\\/?s={search_term_string}\"},\"query-input\":{\"@type\":\"PropertyValueSpecification\",\"valueRequired\":true,\"valueName\":\"search_term_string\"}}],\"inLanguage\":\"fr-FR\"},{\"@type\":\"Organization\",\"@id\":\"https:\\\/\\\/hepatochem.com\\\/fr\\\/#organization\",\"name\":\"HepatoChem\",\"url\":\"https:\\\/\\\/hepatochem.com\\\/fr\\\/\",\"logo\":{\"@type\":\"ImageObject\",\"inLanguage\":\"fr-FR\",\"@id\":\"https:\\\/\\\/hepatochem.com\\\/fr\\\/#\\\/schema\\\/logo\\\/image\\\/\",\"url\":\"https:\\\/\\\/i0.wp.com\\\/xn8.6f7.myftpupload.com\\\/wp-content\\\/uploads\\\/2019\\\/12\\\/HepatoChem-logo-lowres.png?fit=500%2C89&ssl=1\",\"contentUrl\":\"https:\\\/\\\/i0.wp.com\\\/xn8.6f7.myftpupload.com\\\/wp-content\\\/uploads\\\/2019\\\/12\\\/HepatoChem-logo-lowres.png?fit=500%2C89&ssl=1\",\"width\":500,\"height\":89,\"caption\":\"HepatoChem\"},\"image\":{\"@id\":\"https:\\\/\\\/hepatochem.com\\\/fr\\\/#\\\/schema\\\/logo\\\/image\\\/\"},\"sameAs\":[\"https:\\\/\\\/x.com\\\/evoluchem\",\"https:\\\/\\\/www.linkedin.com\\\/company\\\/2420256\"]}]}<\/script>\n<!-- \/ Yoast SEO plugin. -->","yoast_head_json":{"title":"PhotoRedOx Box\u2122 | Photor\u00e9acteur PhotoRedox par HepatoChem","description":"D\u00e9couvrez le photor\u00e9acteur PhotoRedox d\u2019HepatoChem. C\u2019est la solution id\u00e9ale pour toute installation de photochimie en laboratoire.","robots":{"index":"index","follow":"follow","max-snippet":"max-snippet:-1","max-image-preview":"max-image-preview:large","max-video-preview":"max-video-preview:-1"},"canonical":"https:\/\/hepatochem.com\/fr\/photoreacteurs-accessoires-led-et-plus-encore\/photoredox-box\/","twitter_misc":{"Dur\u00e9e de lecture estim\u00e9e":"71 minutes"},"schema":{"@context":"https:\/\/schema.org","@graph":[{"@type":"WebPage","@id":"https:\/\/hepatochem.com\/fr\/photoreacteurs-accessoires-led-et-plus-encore\/photoredox-box\/","url":"https:\/\/hepatochem.com\/fr\/photoreacteurs-accessoires-led-et-plus-encore\/photoredox-box\/","name":"PhotoRedOx Box\u2122 | Photor\u00e9acteur PhotoRedox par HepatoChem","isPartOf":{"@id":"https:\/\/hepatochem.com\/fr\/#website"},"primaryImageOfPage":{"@id":"https:\/\/hepatochem.com\/fr\/photoreacteurs-accessoires-led-et-plus-encore\/photoredox-box\/#primaryimage"},"image":{"@id":"https:\/\/hepatochem.com\/fr\/photoreacteurs-accessoires-led-et-plus-encore\/photoredox-box\/#primaryimage"},"thumbnailUrl":"https:\/\/hepatochem.com\/wp-content\/uploads\/2023\/09\/PhotoRedOx-Box-on-blend-9.27.23-1-e1695835529712.jpg","datePublished":"2022-08-06T19:39:48+00:00","dateModified":"2026-06-02T12:00:05+00:00","description":"D\u00e9couvrez le photor\u00e9acteur PhotoRedox d\u2019HepatoChem. C\u2019est la solution id\u00e9ale pour toute installation de photochimie en laboratoire.","breadcrumb":{"@id":"https:\/\/hepatochem.com\/fr\/photoreacteurs-accessoires-led-et-plus-encore\/photoredox-box\/#breadcrumb"},"inLanguage":"fr-FR","potentialAction":[{"@type":"ReadAction","target":["https:\/\/hepatochem.com\/fr\/photoreacteurs-accessoires-led-et-plus-encore\/photoredox-box\/"]}]},{"@type":"ImageObject","inLanguage":"fr-FR","@id":"https:\/\/hepatochem.com\/fr\/photoreacteurs-accessoires-led-et-plus-encore\/photoredox-box\/#primaryimage","url":"https:\/\/hepatochem.com\/wp-content\/uploads\/2023\/09\/PhotoRedOx-Box-on-blend-9.27.23-1-e1695835529712.jpg","contentUrl":"https:\/\/hepatochem.com\/wp-content\/uploads\/2023\/09\/PhotoRedOx-Box-on-blend-9.27.23-1-e1695835529712.jpg","width":1370,"height":1080,"caption":"A blue box with a cup on top of it."},{"@type":"BreadcrumbList","@id":"https:\/\/hepatochem.com\/fr\/photoreacteurs-accessoires-led-et-plus-encore\/photoredox-box\/#breadcrumb","itemListElement":[{"@type":"ListItem","position":1,"name":"Photor\u00e9acteurs, accessoires, LED et plus encore","item":"https:\/\/hepatochem.com\/fr\/photoreacteurs-accessoires-led-et-plus-encore\/"},{"@type":"ListItem","position":2,"name":"PhotoRedOx Box&#x2122;"}]},{"@type":"WebSite","@id":"https:\/\/hepatochem.com\/fr\/#website","url":"https:\/\/hepatochem.com\/fr\/","name":"HepatoChem","description":"Reinventing Chemistry for Life Sciences","publisher":{"@id":"https:\/\/hepatochem.com\/fr\/#organization"},"potentialAction":[{"@type":"SearchAction","target":{"@type":"EntryPoint","urlTemplate":"https:\/\/hepatochem.com\/fr\/?s={search_term_string}"},"query-input":{"@type":"PropertyValueSpecification","valueRequired":true,"valueName":"search_term_string"}}],"inLanguage":"fr-FR"},{"@type":"Organization","@id":"https:\/\/hepatochem.com\/fr\/#organization","name":"HepatoChem","url":"https:\/\/hepatochem.com\/fr\/","logo":{"@type":"ImageObject","inLanguage":"fr-FR","@id":"https:\/\/hepatochem.com\/fr\/#\/schema\/logo\/image\/","url":"https:\/\/i0.wp.com\/xn8.6f7.myftpupload.com\/wp-content\/uploads\/2019\/12\/HepatoChem-logo-lowres.png?fit=500%2C89&ssl=1","contentUrl":"https:\/\/i0.wp.com\/xn8.6f7.myftpupload.com\/wp-content\/uploads\/2019\/12\/HepatoChem-logo-lowres.png?fit=500%2C89&ssl=1","width":500,"height":89,"caption":"HepatoChem"},"image":{"@id":"https:\/\/hepatochem.com\/fr\/#\/schema\/logo\/image\/"},"sameAs":["https:\/\/x.com\/evoluchem","https:\/\/www.linkedin.com\/company\/2420256"]}]}},"jetpack_sharing_enabled":true,"_links":{"self":[{"href":"https:\/\/hepatochem.com\/fr\/wp-json\/wp\/v2\/pages\/23974","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/hepatochem.com\/fr\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/hepatochem.com\/fr\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/hepatochem.com\/fr\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/hepatochem.com\/fr\/wp-json\/wp\/v2\/comments?post=23974"}],"version-history":[{"count":5,"href":"https:\/\/hepatochem.com\/fr\/wp-json\/wp\/v2\/pages\/23974\/revisions"}],"predecessor-version":[{"id":23985,"href":"https:\/\/hepatochem.com\/fr\/wp-json\/wp\/v2\/pages\/23974\/revisions\/23985"}],"up":[{"embeddable":true,"href":"https:\/\/hepatochem.com\/fr\/wp-json\/wp\/v2\/pages\/23917"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/hepatochem.com\/fr\/wp-json\/wp\/v2\/media\/23975"}],"wp:attachment":[{"href":"https:\/\/hepatochem.com\/fr\/wp-json\/wp\/v2\/media?parent=23974"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}