Issue 11, 2017

Synthesis of N,N-disubstituted 2-aminothiophenes by the cyclization of gem-difluoroalkenes with β-keto thioamides

Abstract

A novel and effective method for the construction of highly functionalized aminothiophenes via the cyclization of gem-difluoroalkenes with β-keto tertiary thioamides is described. The reactions proceed smoothly with the assistance of K2CO3 under transition-metal-free conditions, affording a variety of valuable N,N-disubstituted 2-aminothiophenes in moderate to good yields.

Graphical abstract: Synthesis of N,N-disubstituted 2-aminothiophenes by the cyclization of gem-difluoroalkenes with β-keto thioamides

Supplementary files

Article information

Article type
Paper
Submitted
15 Feb 2017
Accepted
24 Feb 2017
First published
24 Feb 2017

Org. Biomol. Chem., 2017,15, 2436-2442

Synthesis of N,N-disubstituted 2-aminothiophenes by the cyclization of gem-difluoroalkenes with β-keto thioamides

X. Zhang, M. Wu, J. Zhang and S. Cao, Org. Biomol. Chem., 2017, 15, 2436 DOI: 10.1039/C7OB00368D

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