| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1255730 | Chinese Chemical Letters | 2011 | 4 Pages |
Abstract
A stereoselective and effective method for the synthesis of vinyl thioethers has been developed. This method is based on the Michael addition of ethanethiol to various alkynyl ketones using 10Â mol% of tributylphosphine as catalyst. Most of alkynyl ketones react with ethanethiol in this system to yield mainly Z-isomer of vinyl thioether adducts, only in one case mainly E-isomer of vinyl thioether adducts was observed.
Related Topics
Physical Sciences and Engineering
Chemistry
Chemistry (General)
Authors
Shen Zhao, Qing Fa Zhou, Jia Zhi Liu, Wei Fang Tang, Tao Lu,