期刊
ORGANIC LETTERS
卷 24, 期 9, 页码 1865-1870出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.2c00478
关键词
-
资金
- National Natural Science Foundation of China [22071211, 21801076]
- Open Research Fund of School of Chemistry and Chemical Engineering of Henan Normal University [2022C02]
In this study, sulfinates were successfully used as sulfenylating reagents in C-S couplings through visible-light-induced photo/nickel dual catalysis under base- and external reductant-free conditions. The method showed high selectivity and tolerance towards various functionalities.
The C-S bond formation from aryl halides and thiols has been well established under various catalytic systems. In this work, user-friendly sulfinates have been exploited as an efficient sulfenylating reagent in the C-S couplings through visible-light-induced photo/nickel dual catalysis under base- and external reductant-free conditions. A large number of aryl sulfide products were accessed with high selectivity and high tolerance of various functionalities.
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