Issue 37, 2015

Stereoselective synthesis and reaction of gold(i) (Z)-enethiolates

Abstract

Bench-top-storable (Z)-enethiol reagents: gold (Z)-1-decenylthiolates were synthesized stereoselectively in high yields. They are stable upon storage at room temperature without protection from light, and react smoothly with various alkyl halides, α,β-unsaturated ketones, and electron-deficient aryl halides with excellent stereoselectivity.

Graphical abstract: Stereoselective synthesis and reaction of gold(i) (Z)-enethiolates

Supplementary files

Article information

Article type
Communication
Submitted
09 Mar 2015
Accepted
01 Apr 2015
First published
01 Apr 2015

Chem. Commun., 2015,51, 7962-7965

Author version available

Stereoselective synthesis and reaction of gold(I) (Z)-enethiolates

K. Miyamoto, M. Hirobe, M. Uchiyama and M. Ochiai, Chem. Commun., 2015, 51, 7962 DOI: 10.1039/C5CC02000J

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