Visible-Light-Mediated Organocatalyzed Thiol–Ene Reaction Initiated by a Proton-Coupled Electron Transfer Full article
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Journal of Organic Chemistry
ISSN: 1520-6904 , E-ISSN: 0022-3263 |
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| Output data | Year: 2019, Volume: 84, Number: 12, Pages: 8337-8343 Pages count : 7 DOI: 10.1021/acs.joc.9b01331 | ||
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Abstract:
A convenient method for performing a thiol–ene reaction is described. The reaction is performed under blue-light irradiation and catalyzed by photoactive Lewis basic molecules such as acridine orange or naphthalene-fused N-acylbenzimidazole. It is believed that the process is initiated by a proton-coupled electron transfer process within the complex between the thiol and the Lewis basic catalyst.
Cite:
Levin V.V.
, Dilman A.D.
Visible-Light-Mediated Organocatalyzed Thiol–Ene Reaction Initiated by a Proton-Coupled Electron Transfer
Journal of Organic Chemistry. 2019. V.84. N12. P.8337-8343. DOI: 10.1021/acs.joc.9b01331 WOS Scopus OpenAlex
Visible-Light-Mediated Organocatalyzed Thiol–Ene Reaction Initiated by a Proton-Coupled Electron Transfer
Journal of Organic Chemistry. 2019. V.84. N12. P.8337-8343. DOI: 10.1021/acs.joc.9b01331 WOS Scopus OpenAlex
Identifiers:
| Web of science: | WOS:000473116200077 |
| Scopus: | 2-s2.0-85067682847 |
| OpenAlex: | W2945429402 |