Diaryl Selenide Catalyzed Vicinal Trifluoromethylthioamination of Alkenes.

Abstract

An efficient approach to vicinal trifluoromethylthioamination of alkenes with a broad substrate scope catalyzed by electron-rich diaryl selenide has been developed. This intermolecular amination strategy was successfully applied to SCF3-esterification of alkenes using weak acids as nucleophiles. 
DOI: 10.1021/acs.orglett.5b01727

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Cite this paper

@article{Luo2015DiarylSC, title={Diaryl Selenide Catalyzed Vicinal Trifluoromethylthioamination of Alkenes.}, author={Jie Luo and Zechen Zhu and Yannan Liu and Xiaodan Zhao}, journal={Organic letters}, year={2015}, volume={17 14}, pages={3620-3} }