PhotoRedOx Box™

The EvoluChem PhotoRedOx Box™ is the photochemistry photoreactor choice for the chemist who seeks to standardize laboratory photochemical setups economically. A flexible design allows interchangeable LEDs from 365 nm to 808 nm and a wide variety of vials.

This photochemistry photoreactor (US Patent #10,906,022) is designed to facilitate photochemical experimentation. It is compatible with most vial formats (0.3 ml, 2 ml, 4 ml and 20 ml vials) and its compact design allows for use with any stirring plate. A built-in fan keeps the reaction conditions at room temperature.

Easy setup and compact design

Fit multiple vial sizes

More than 300 publication since 2018

(1)      Seefeldt, P.; Villinger, A.; Brasholz, M. Photoredox-Catalyzed Carbon Radical Generation from α-Keto- N , O -Acetals : Synthesis of Functionalized Azepino [ 1 , 2- a ] Indoles and Azepino [ 1 , 2- a ] Furo [ 3 , 2- b ] Indoles. Adv. Synth. Catal. 2024, 366 (1), 24–30.

(2)      Adrián Luguera Ruiz; Mariani, E.; Stefano Protti; Fagnoni, M. Photoredox Catalyzed Release of Carbon-Based Radicals from 2- Substituted-1,3-Imidazolidines. Org. Chem. Front. 2024. https://doi.org/10.1039/D3QO01856C.

(3)      Fu-Peng Wu, Chetan C. Chintawar, Remy Lalisse, Poulami Mukherjee, Subhabrata Dutta, Jasper Tyler, Constantin G. Daniliuc, O. G. & F. G. Ring Expansion of Indene by Photoredox- Enabled Functionalized Carbon-Atom Insertion. Nat. Catal. 2024.

(4)      Dutta, S.; Lee, D.; Ozols, K.; Daniliuc, C. G.; Shintani, R.; Glorius, F. Photoredox-Enabled Dearomative [2π + 2σ] Cycloaddition of Phenols. J. Am. Chem. Soc. 2024, 1–116. https://doi.org/10.1021/jacs.3c12894.

(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. Org. Lett. 2024, 10–13. https://doi.org/10.1021/acs.orglett.3c03684.

(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. Org. Lett. 2024.

(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. J. Am. Chem. Soc 2024. https://doi.org/10.1021/jacs.3c13982.

(8)      Subhabrata Dutta, Yi-Lin Lu, Johannes E. Erchinger, Huiling Shao, Emanuel Studer, Felix Schäfer, Huamin Wang, Debanjan Rana, Constantin G. Daniliuc, K. N. Houk,* and Frank Glorius Shao, Emanuel Studer, Felix Schäfer, Huamin Wang, Debanjan Rana, Constantin, and F. G. Double Strain-Release[2π+2σ]-Photocycloaddition. J. Am. Chem. Soc 2024, No. 1, 1–5.

(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. J. Am. Chem. Soc 2024, 1–87. https://doi.org/10.1021/acs.joc.3c02709.

(10)    Igor A. Lavrinchenko , Egor A. Nikiforov , Timofey D. Moseev , Mikhail V. Varaksin ∗ , Anton N. Tsmokalyuk , Thomas V. Nechaev , Valery N. Charushin, O. N. Synthesis, Photophysical, and AIE Properties of 2H-Imidazole-Derived Push-Pull Fluorophores. Synthesis (Stuttg). 2024.

(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. Nat. Chem. 2024, 1–18. https://doi.org/10.1038/s41557-023-01414-8.

(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. J. Org. Chem. 2024, 1–28. https://doi.org/10.1021/acs.joc.3c02351.

(13)    Seefeldt, P.; Edelmann, L.; Prudlik, A.; Villinger, A.; Francke, R.; Brasholz, M. Photoinduced Tandem C-O Bond Reduction / Ketyl Radical Addition Reactions of α -Keto- N , O -Acetals Enabled by Proton-Coupled Electron Transfer. ChemPhotoChem 2024.

(14)    Han, G.; You, J.; Choi, J.; Joo, E. N -Iminopyridinium Compounds in Giese Reaction : Photoinduced Homolytic N-N and C-C Bond Cleavage for Cyanoalkyl Radical Generation. Org. Lett. 2024, 1–99.

(15)    Bonfils, P. De; Nun, P.; Coeffard, V. Unsymmetrical Anthracene Platforms as Singlet Oxygen Batteries : Effects of Substituents on Photooxygenation and Endoperoxide Thermolysis. European J. Org. Chem. 2024, 202400099 (1), 4–5. https://doi.org/10.1002/ejoc.200490000.

(16)    Tagami, T.; Kawamura, S.; Sodeoka, M. Aerobic Photoredox Catalyzed Oxamate Ester Synthesis from Bromodifluoroacetate Esters. European J. Org. Chem. 2024.

(17)    Laskar, R.; Dutta, S.; Spies, J. C.; Mukherjee, P.; Rentería-gómez, Á. Γ‑Amino Alcohols via Energy Transfer Enabled Brook Rearrangement. J. Am. Chem. Soc 2024.

(18)    Magkoev, T. T.; Demidov, O. P.; Abaev, V. T.; Uchuskin, M. G.; Chalikidi, P. N. Unveiling Orthogonal Reactivity of Substituted 2‑(2- Azidostyryl)Furans: Thermolysis and Photolysis versus Catalysis. J. Org. Chem. 2024, 1–68. https://doi.org/10.1021/acs.joc.4c00355.

(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. J. Med. Chem. 2024. https://doi.org/10.1021/acs.jmedchem.3c02397.

(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]. ChemRxiv. Prepr. 2024.

(21)    Krax, R.; Menneking, K.; Sajapin, J.; Hellwig, M. Identification of β-Aspartic Semialdehyde and Homocysteine as Major Reaction Products of Riboflavin-Sensitized Photooxidation of Peptide-Bound Methionine. Eur. Food Res. Technol. 2024. https://doi.org/10.1007/s00217-024-04540-w.

(22)    Jonathan Da Luz , Michaela Čierna , Bradley D. Cooper , Thomas D. Harris , Ethan R. X. Lim , Jonathan R. Carney, M. J. J. Denitrative Sulfonylation of Nitroarenes with Sodium Sulfinates. Synthesis (Stuttg). 2024.

(23)    Lilian Geniller, Marc Taillefer, Eric Clot, Florian Jaroschik, and A. P. Photocatalyzed Formation of Gem‐difluoroalkenes Using Oxime Esters. Adv. Synth. Catal. 2024, 1–23.

(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. Org. Lett. 2024, 2 (1), 1–5. https://doi.org/10.1021/acs.orglett.4c01216.

(25)    Ortalli, S.; Ford, J.; Trabanco, A. A.; Tredwell, M.; Gouverneur, V. Photoredox Nucleophilic ( Radio ) Fluorination of Alkoxyamines. J. Am. Chem. Soc 2024, 0–5. https://doi.org/10.1021/jacs.4c02474.

(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 ́. Appl. Mater. Interfaces 2024, 1–34. https://doi.org/10.1021/acsami.4c03369.

(27)    Hu, T.; Fagué, V.; Bouyssi, D.; Monteiro, N.; Amgoune, A. Hydride-Free Reduction of Propargyl Electrophiles: A Nickel-Catalyzed Photoredox Strategy for Allene Synthesis. Green Chem. 2024. https://doi.org/10.1039/d4gc00984c.

(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. Microbiol. Spectr. 2024, No. April.

(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. J. Am. Chem. Soc 2024. https://doi.org/10.1021/jacs.4c02553.

(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. ACS MacroLetters 2024. https://doi.org/10.1021/acsmacrolett.4c00083.

(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. Dalt. Trans. 2024.

(32)    Tambe, S. D.; Hwang, H. S.; Park, E.; Cho, E. J. Dual Photoredox and Nickel Catalysis in Regioselective Diacylation : Exploring the Versatility of Nickel Oxidation States in Allene Activation. Org. Lett. 2024.

(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 – ( 2-Phenyl ) Benzoyl Groups. Asian J. Chem. 2024.

(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. Chem. Sci. 2024, 2 (100 mL), 2–6. https://doi.org/10.1038/scientificamerican10271883-6511csupp.

(35)    Lasky, M. R.; Liu, E.; Remy, M. S.; Sanford, M. S. Visible-Light Photocatalytic C − H Amination of Arenes Utilizing Acridine − Lewis Acid Complexes. J. Am. Chem. Soc 2024. https://doi.org/10.1021/cm504475k.

(36)    Tyler, J. L.; Schäfer, 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 [2π+2σ] Cycloaddition Reactions. J. Am. Chem. Soc. 2024.

(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. Nat. Commun. 2024, 15, 4351. https://doi.org/10.1038/s41467-024-48148-w.

(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. Sci. Technol. Adv. Mater. 2024, 25 (1). https://doi.org/10.1080/14686996.2024.2322458.

(39)    Nugent, J.; López-francés, A.; Sterling, A. J.; Yi, M.; Frank, N.; James, J.; Anderson, E. A. α-Amino Bicycloalkylation through Organophotoredox Catalysis. Chem. Sci. 2024. https://doi.org/10.1039/D4SC01368A.

(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 *. J. Org. Chem. 2024, 11 (1), 1–5. https://doi.org/10.1021/acs.joc.4c00721.

(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 . J. Org. Chem. 2024, 1–166.

(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. Nanoscale 2024, 16 (1), 138–151. https://doi.org/10.1039/d3nr04915a.

(43)    Pijper, B.; Saavedra, L. M.; Lanzi, M.; Alonso, M.; Fontana, A.; Serrano, M.; Gómez, J. E.; Kleij, A. W.; Alcázar, J.; Cañellas, S. Addressing Reproducibility Challenges in High-Throughput Photochemistry. JACS Au 2024. https://doi.org/10.1021/jacsau.4c00312.

(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. Nature 2024, 626 (7999), 542–548. https://doi.org/10.1038/s41586-023-06932-6.

(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. ACS Sustain. Chem. Eng. 2024, 1–6. https://doi.org/10.1021/acssuschemeng.4c02042.

(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−Organic Framework For Tandem Metallaphotocatalysis. Appl. Mater. Interfaces 2024.

(47)    Andrews, J. A.; Woodger, R. G.; Palmer, C. F.; Poole, D. L.; Willis, M. C. Exploiting Amine-Sulfinylamine Exchange for Photo-Decarboxylative Sulfinamidation. Angew. Chem. Int. Ed. 2024.

(48)    Yusuke Miyamoto, Sho Murakami, Yuto Sumida, Go Hirai, H. O. Radical C-Glycosylation Using Photoexcitable Unprotected Glycosyl Borate. Chem. A Eur. J. 2024, 1–134.

(49)    Cahard, D.; Marie, N.; Ma, J.-A.; Tognetti, V. Photocatalyzed Cascade Hydrogen Atom Transfers for Assembly of Multi‐substituted Α‐SCF3 and Α‐SCF2H Cyclopentanones. Angew. Chemie Int. Ed. 2024. https://doi.org/10.1002/anie.202407689.

(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. Adv. Synth. Catal. 2024.

(51)    Venditto, N. J.; Boerth, J. A. Deoxy-Arylation of Amides via a Tandem Hydrosilylation/Radical- Radical Coupling Sequence. Org. Lett. 2024, 26 (17), 3617–3621. https://doi.org/10.1021/acs.orglett.4c01121.

(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. European J. Org. Chem. 2024, 27 (20), 1–7. https://doi.org/10.1002/ejoc.202400191.

(53)    Chen, X.; Li, H.; Kramer, S. Photoinduced Copper-Catalyzed Enantioselective Allylic C ( Sp 3 )– H Oxidation of Acyclic 1-Aryl-2-Alkyl Alkenes as Limiting Substrates. Angew. Chem. Int. Ed. 2024, 1–102.

(54)    Li, M.; Yuan, Y.; Harrison, W.; Zhang, Z.; Zhao, H. Asymmetric Photoenzymatic Incorporation of Fluorinated Motifs into Olefins. Science (80-. ). 2024, 385 (6707), 416–421. https://doi.org/10.1126/science.adk8464.

(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 α-Fluorovinyl-C-Glycosylation Strategy to Create Glycan Analogs with Altered Biological Activities. J. Am. Chem. Soc. 2024, 146 (3), 2237–2247. https://doi.org/10.1021/jacs.3c12581.

(56)    Jhun, B. H.; Jang, J.; Lee, S.; Cho, E. J.; You, Y. Efficient Photoredox Catalysis in C–C Cross-Coupling Reactions by Two-Coordinated Au(I) Complex. Nat. Commun. 2024, 15 (1), 1–12. https://doi.org/10.1038/s41467-024-50979-6.

(57)    Harfouche, N.; Marie, P.; Dragoe, D.; Le, H.; Thébault, P.; Bilot, C.; Fouchet, A.; Rouden, J.; Baudoux, J.; Lepoittevin, B. Antibacterial Zirconia Surfaces from Organocatalyzed Atom-Transfer Radical Polymerization. Materials (Basel). 2024, 17 (8). https://doi.org/10.3390/ma17081775.

(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 – and CHF-Linked Analogs. J. Org. Chem. 2024. https://doi.org/10.1021/acs.joc.4c01143.

(59)    Noyuri Kudo‡ , Suzuka Chiba‡ , Shunsuke Ono , Masataka Nagatoishi , Makoto Yoritate , Satoru Karasawa , Kazuteru Usui∗, G. H. Stereoselective Synthesis of C-Aryl-α-Glycosides by Reductive C(Sp2)-C(Sp3) Cross-Coupling Reaction. Synlett 2024.

(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. Chem. Sci. 2024. https://doi.org/10.1039/d4sc02511c.

(61)    Wu, F.; Tyler, J. L.; Daniliuc, C. G.; Glorius, F. Atomic Carbon Equivalent : Design and Application to Diversity- Generating Skeletal Editing from Indoles to 3-Functionalized Quinolines. ACS Catal. 2024, 1–189.

(62)    Emily R. Wearing, Yu-Cheng Yeh, Gianmarco G. Terrones, Seren G. Parikh, Ilia Kevlishvili, Heather J. Kulik, and C. S. S. Visible Light–Mediated Aza Paternò–Büchi Reaction of Acyclic Oximes and Alkenes to Azetidines Emily. Science 2024, 384. https://doi.org/10.1126/science.adn6384.

(63)    Boudry, E.; Bourdreux, F.; Marrot, J.; Moreau, X.; Ghiazza, C. Dearomatization of Pyridines: Photochemical Skeletal Enlargement for the Synthesis of 1,2-Diazepines. J. Am. Chem. Soc. 2024, 146 (4), 2845–2854. https://doi.org/10.1021/jacs.3c14467.

(64)    Zhang, T.; Rabeah, J.; Das, S. Red-Light-Mediated Copper-Catalyzed Photoredox Catalysis Promotes Regioselectivity Switch in the Difunctionalization of Alkenes. Nat. Commun. 2024, 15 (1), 1–10. https://doi.org/10.1038/s41467-024-49514-4.

(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. J. Inorg. Biochem. 2024, 259 (June), 110984. https://doi.org/10.1016/j.jinorgbio.2024.112657.

(66)    Tagami, K.; Nakayama, M.; Kanbara, T.; Cahard, D.; Yajima, T. 10-Phenylphenothiazine-Organophotocatalyzed Bromo-Perfluoroalkylation of Unactivated Olefins. J. Org. Chem. 2024, 89 (10), 7084–7094. https://doi.org/10.1021/acs.joc.4c00470.

(67)    Di Terlizzi, L.; Martinelli, A.; Merli, D.; Protti, S.; Fagnoni, M. Arylazo Sulfones as Nonionic Visible-Light Photoacid Generators. J. Org. Chem. 2023, 88 (10), 6313–6321. https://doi.org/10.1021/acs.joc.2c01248.

(68)    Fortier, L.; Gosset, C.; Lefebvre, C.; Pellegrini, S.; Pélinski, L.; Bousquet, T. Photocatalyzed Synthesis of 3-Substituted Phthalides: A Key Access to (±)-Herbaric Acid. European J. Org. Chem. 2023, 26 (4), 1–63. https://doi.org/10.1002/ejoc.202201247.

(69)    Laze, L.; Romero, P.; Bosque, I.; Gonzalez-Gomez, J. C. Oxidative Coupling of 4‐Hydroxycoumarins with Quinoxalin‐2 1H ‐ones Induced by Visible Light. European J. Org. Chem. 2023, 2 (Cdc), 125–127. https://doi.org/10.2307/j.ctv1dwq04c.8.

(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. Inorg. Chem. Commun. 2023.

(71)    Erchinger, J. E.; Hoogesteger, R.; Laskar, R.; Dutta, S.; Hümpel, C.; Rana, D.; Daniliuc, C. G.; Glorius, F. EnT-Mediated N – S Bond Homolysis of a Bifunctional Reagent Lead- Ing to Aliphatic Sulfonyl Fluorides. J. Am. Chem. Soc 2023, ASAP.

(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. Macromolecules 2023, Accepted. https://doi.org/10.1021/acs.macromol.2c02025.

(73)    Liu, C.; Shen, N.; Shang, R. Photocatalytic Defluoroalkylation of Trifluoroacetates with Alkenes Using 4-(Acetamido)Thiophenol. Synthesis (Stuttg). 2023.

(74)    Chen, X.; Lian, Z.; Kramer, S. Enantioselective Intermolecular Radical Amidation and Amination of Benzylic C − H Bonds via Dual Copper and Photocatalysis. Angew. Chemie Int. Ed. 2023. https://doi.org/10.1002/anie.202217638.

(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. Chem. Sci. 2023. https://doi.org/10.1039/x0xx00000x.

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