Issue 66, 2020

Stereoselective aminosulfonylation of alkynes: an approach to access (Z)-β-amino vinylsulfones

Abstract

The stereoselective sulfur–nitrogen difunctionalization (aminosulfonylation) across the alkyne framework in a syn mode is accomplished using sodium sulfinates and azoles, in the presence of I2/base. This strategy is applicable to a variety of terminal alkynes, sodium sulfinates, and azoles as reaction partners, affording (Z)-β-amino vinylsulfones in good yields.

Graphical abstract: Stereoselective aminosulfonylation of alkynes: an approach to access (Z)-β-amino vinylsulfones

Supplementary files

Article information

Article type
Communication
Submitted
26 May 2020
Accepted
08 Jul 2020
First published
16 Jul 2020

Chem. Commun., 2020,56, 9561-9564

Stereoselective aminosulfonylation of alkynes: an approach to access (Z)-β-amino vinylsulfones

M. Y. Ansari, S. Swarnkar and A. Kumar, Chem. Commun., 2020, 56, 9561 DOI: 10.1039/D0CC03726E

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