Journal
ORGANIC LETTERS
Volume 20, Issue 13, Pages 3829-3832Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.8b01418
Keywords
-
Categories
Funding
- Natural Science Foundation of China [21572118, JQ201505]
- Natural Science Foundation of Shandong Province [21572118, JQ201505]
- Shandong University
Ask authors/readers for more resources
An efficient electrophilic persulfuration reaction leading to unsymmetrical disulfides and polysulfides has been developed. Various nucleophiles, including aryl boronic acids, beta-keto esters, and thiols, can be used as substrates. The notable features of this method include very simple and practical conditions, general scope, and inexpensive copper catalysts.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available
Share Paper
