Issue 23, 2021

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

Abstract

The addition reaction of thiol to vinyl azide has been extensively studied. Variously substituted aryl thiols are all viable for this coupling process. The scope of the other partner is successfully expanded from α-aryl vinyl azide to α-alkyl vinyl azide. A thiol–vinyl azide coupling/cyclization cascade is realized with substituted aryl vinyl azides carrying a 2-methoxycarbonyl group. The value of β-ketosulfide products was demonstrated by its application in S-heterocycle synthesis.

Graphical abstract: 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

Supplementary files

Article information

Article type
Paper
Submitted
22 Feb 2021
Accepted
04 May 2021
First published
21 May 2021

Org. Biomol. Chem., 2021,19, 5169-5176

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

Y. Wang, Y. Wang, X. Liang, M. Shen, H. Xu and D. Xu, Org. Biomol. Chem., 2021, 19, 5169 DOI: 10.1039/D1OB00328C

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