An aryl thiol–vinyl azide coupling reaction and a thiol–vinyl azide coupling/cyclization cascade: efficient synthesis of β-ketosulfides and arene-fused 5-methylene-2-pyrrolidinone derivatives-Reference-Cited by-同舟云学术

An aryl thiol–vinyl azide coupling reaction and a thiol–vinyl azide coupling/cyclization cascade: efficient synthesis of β-ketosulfides and arene-fused 5-methylene-2-pyrrolidinone derivatives

Published:2021 Issue:23 Volume:19 Page:5169-5176
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Wang Yong¹²³⁴⁵,Wang Yu-Jiao¹²³⁴⁵,Liang Xian-Chen¹²³⁴⁵,Shen Mei-Hua¹²³⁴⁵^ORCID,Xu Hua-Dong¹²³⁴⁵^ORCID,Xu Defeng¹²³⁴⁵

Affiliation:

1. Jiangsu Key Laboratory of Advanced Catalytic Materials & Technology

2. School of Pharmacy

3. Changzhou University

4. Changzhou

5. China

Abstract

A radical addition–fragmentation intermediate of vinyl azide can be intercepted by a neighbouring ester group. β-Ketosulfides could be a convenient platform for S-heterocycle synthesis.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2021/OB/D1OB00328C

Reference74 articles.

1. Application of Vinyl Azides in Chemical Synthesis: A Recent Update

2. α-Substituted vinyl azides: an emerging functionalized alkene

3. Reactivities of vinyl azides and their recent applications in nitrogen heterocycle synthesis

4. Vinyl Azides as Versatile Synthons for the Synthesis of Nitrogen-containing Heterocycles

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