Issue 62, 2022

Electrochemical alkene azidocyanation via 1,4-nitrile migration

Abstract

An electrochemical method for the azidocyanation of alkenes via 1,4-nitrile migration has been developed. This organic oxidant free method is applicable across various alkene containing cyanohydrins, and provides access to a broad range of synthetically useful 1,2-azidonitriles (28 examples). This methodology was extended to an electrochemical alkene sulfonylcyanation procedure, as well as to access a trifunctionalized hexanenitrile from a malononitrile starting material. The orthogonal derivatization of the products was also demonstrated through chemoselective transformations.

Graphical abstract: Electrochemical alkene azidocyanation via 1,4-nitrile migration

Supplementary files

Article information

Article type
Communication
Submitted
25 May 2022
Accepted
06 Jul 2022
First published
13 Jul 2022
This article is Open Access
Creative Commons BY license

Chem. Commun., 2022,58, 8658-8661

Electrochemical alkene azidocyanation via 1,4-nitrile migration

A. C. Seastram, M. D. Hareram, T. M. B. Knight and L. C. Morrill, Chem. Commun., 2022, 58, 8658 DOI: 10.1039/D2CC02958H

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