| Literature DB >> 30489090 |
Prashant Chakrasali1,2, Kyuneun Kim1,2, Young-Sik Jung1,2, Hyejin Kim1, Soo Bong Han1,2.
Abstract
Herein, a one-step chlorosulfonylation of alkynes via a photocatalytic redox process is described. A variety of commercially available sulfonyl chlorides can be applied for the generation of sulfonyl radical species under visible-light irradiation. Regio- and stereoselective addition of the sulfonyl radical and chloride leads to the efficient formation of ( E)-selective β-chlorovinyl sulfones from a broad range of terminal and internal alkynes. The reported method represents an operationally simple and mild way to furnish vinyl sulfones.Entities:
Year: 2018 PMID: 30489090 DOI: 10.1021/acs.orglett.8b03273
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005