Issue 72, 2017

K2CO3-promoted aerobic oxidative cross-coupling of trialkyl phosphites with thiophenols

Abstract

Convenient, practical and economical phosphorylation of thiols has been achieved via halogen- and metal-free K2CO3-promoted aerobic oxidative cross-coupling of trialkyl phosphites, dimethyl phenylphosphonite, or methyl diphenylphosphinite with thiophenols using air as the oxidant at room temperature. This transformation provides a straightforward route to the construction of phosphorus–sulfur bonds with wide functional group compatibility, which affords phosphorothioates in up to 94% yield.

Graphical abstract: K2CO3-promoted aerobic oxidative cross-coupling of trialkyl phosphites with thiophenols

Supplementary files

Article information

Article type
Paper
Submitted
16 अगस्त 2017
Accepted
18 सितम्बर 2017
First published
25 सितम्बर 2017
This article is Open Access
Creative Commons BY license

RSC Adv., 2017,7, 45416-45419

K2CO3-promoted aerobic oxidative cross-coupling of trialkyl phosphites with thiophenols

C. Wen, Q. Chen, Y. Huang, X. Wang, X. Yan, J. Zeng, Y. Huo and K. Zhang, RSC Adv., 2017, 7, 45416 DOI: 10.1039/C7RA09057A

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