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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†
Yong Wang,Yu-Jiao Wang,Xian-Chen Liang,Mei-Hua Shen,Hua-Dong Xu,Defeng Xu
Organic & Biomolecular Chemistry Pub Date : 05/21/2021 00:00:00 , DOI:10.1039/D1OB00328C
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
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