Visible-Light-Mediated Organocatalyzed Thiol–Ene Reaction Initiated by a Proton-Coupled Electron Transfer

Visible-Light-Mediated Organocatalyzed Thiol–Ene Reaction Initiated by a Proton-Coupled Electron Transfer Full article

Journal

Journal of Organic Chemistry
ISSN: 1520-6904 , E-ISSN: 0022-3263

Output data

Year: 2019, Volume: 84, Number: 12, Pages: 8337-8343 Pages count : 7 DOI: 10.1021/acs.joc.9b01331

Authors

Levin Vitalij V. ¹ , Dilman Alexander D. ¹

Affiliations

1	N. D. Zelinsky Institute of Organic Chemistry, Leninsky Prospect 47, Moscow 119991, Russian Federation

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.

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

Web of science:	WOS:000473116200077
Scopus:	2-s2.0-85067682847
OpenAlex:	W2945429402

DB	Citing
OpenAlex	34
Scopus	30
Web of science	33