Late-stage trifluoromethylthiolation of benzylic C-H bonds
Fluoroalkylation of C-H bonds is a class of reaction highly sought after in medicinal chemistry. Here, the authors report a regioselective organophotoredox-catalyzed, trifluoromethylthiolation of benzylic C-H bonds for a wide variety of alkyl (hetero)arenes, and demonstrate its utility in continuous...
Main Authors: | Wentao Xu, Wenliang Wang, Tao Liu, Jin Xie, Chengjian Zhu |
---|---|
Format: | Article |
Language: | English |
Published: |
Nature Publishing Group
2019-10-01
|
Series: | Nature Communications |
Online Access: | https://doi.org/10.1038/s41467-019-12844-9 |
Similar Items
-
Transition-metal-free trifluoromethylthiolation–acylation of arynes by insertion into the C–S bonds
by: Chengyao Kimmy Cao, et al.
Published: (2021-02-01) -
Selenide-catalyzed enantioselective synthesis of trifluoromethylthiolated tetrahydronaphthalenes by merging desymmetrization and trifluoromethylthiolation
by: Jie Luo, et al.
Published: (2018-02-01) -
Decarboxylative trifluoromethylthiolation of pyridylacetates
by: Ryouta Kawanishi, et al.
Published: (2021-01-01) -
Bismuth(III)-Promoted Trifluoromethylthiolation of Pyrazolin-5-ones with Trifluoromethanesulfenamide
by: Qingyun Liu, et al.
Published: (2017-11-01) -
Nouvelles avancées en trifluorométhylthiolation et fluoroalkylsélénolation
by: Glenadel, Quentin
Published: (2017)