Copper-Catalyzed Hydroxytrifluoromethylthiolation of Arylpropynones

11Citations
Citations of this article
7Readers
Mendeley users who have this article in their library.

Abstract

Recently, the preparation of fluorinated compounds through difunctionalization strategies has become a hot research area in fluorine chemistry. In this work, a copper-catalyzed hydroxytrifluoromethylthiolation of arylpropynones for the synthesis of the corresponding trifluoromethylthiolated enols was developed. The copper salt and solvent are crucial to the yields of this reaction. Under optimized reaction conditions, a series of trifluoromethylthiolated enols were obtained in moderate to good yields.

Cite

CITATION STYLE

APA

Hu, J., Huang, Y., Xu, X., & Qing, F. (2019). Copper-Catalyzed Hydroxytrifluoromethylthiolation of Arylpropynones. Chinese Journal of Organic Chemistry, 39(1), 177–182. https://doi.org/10.6023/cjoc201808041

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free