An efficient and mild oxidative approach from thiols to sulfonyl derivatives with DMSO/HBr
Author:
Affiliation:
1. State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, Xue Yuan Rd 38, Beijing 100191, China
Abstract
Funder
National Natural Science Foundation of China
Peking University
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2023/SC/D3SC04945K
Reference106 articles.
1. The growing applications of SuFEx click chemistry
2. A Survey of the Role of Noncovalent Sulfur Interactions in Drug Design
3. Sulfonyl fluorides as targets and substrates in the development of new synthetic methods
4. Sulfonyl fluorides as privileged warheads in chemical biology
5. Desulfonylation via Radical Process: Recent Developments in Organic Synthesis
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