Regioselective tandem sulfonylation/cyclization of unsaturated <i>N</i>-substituted enamides with sulfonyl chlorides by copper catalysis-Reference-Cited by-同舟云学术

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Regioselective tandem sulfonylation/cyclization of unsaturated N-substituted enamides with sulfonyl chlorides by copper catalysis

Published:2024 Issue: Volume: Page:
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Ding Ran¹²^ORCID,Wu Tao¹,Ma Tao¹,Ji Wen-Chao¹,Li Zi-Rong¹,Gao Hui³^ORCID

Affiliation:

1. College of Chemistry and Materials Engineering, Anhui Science and Technology University, Bengbu, Anhui, 233100, P. R. China

2. Department of Chemistry, University of Science and Technology of China, Hefei, Anhui, 230026, China

3. School of Chemistry and Materials Science, Huaibei Normal University, Huaibei, Anhui 235000, P. R. China

Abstract

The radical cascade cyclization of vinyl-tethered alkenes has become a promising tool for rapidly assembling nonbenzene-fused cyclic skeletons via the cracking of alkenyl C–H bonds, but this approach has been limited to generate five-membered rings.

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/QO/D4QO01132E

Reference72 articles.

1. Iodine(III) Reagents in Radical Chemistry

2. Recent Advances in Radical Difunctionalization of Simple Alkenes

3. Recent Advances in Radical C–H Activation/Radical Cross-Coupling

4. Addition of CF3 across unsaturated moieties: a powerful functionalization tool

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