Issue 97, 2014

Palladium-catalyzed selective aminoamidation and aminocyanation of alkenes using isonitrile as amide and cyanide sources

Abstract

A mild and efficient palladium-catalyzed intermolecular aminoamidation and aminocyanation reaction of alkenes with a broad substrate scope has been developed. This cyclization process provides a valuable synthetic tool for obtaining substituted indolines, tetrahydroisoquinolines and pyrrolidines in good to excellent yields.

Graphical abstract: Palladium-catalyzed selective aminoamidation and aminocyanation of alkenes using isonitrile as amide and cyanide sources

Supplementary files

Article information

Article type
Communication
Submitted
30 Sep 2014
Accepted
14 Oct 2014
First published
14 Oct 2014

Chem. Commun., 2014,50, 15348-15351

Author version available

Palladium-catalyzed selective aminoamidation and aminocyanation of alkenes using isonitrile as amide and cyanide sources

H. Jiang, H. Gao, B. Liu and W. Wu, Chem. Commun., 2014, 50, 15348 DOI: 10.1039/C4CC07743A

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