Issue 1, 2016

A one-pot amidation of primary nitroalkanes

Abstract

It has been over a half-century since Kornblum demonstrated the conversion of a primary nitroalkane to a carboxylic acid; addition of an amine results in carboxylic acid formation as well. We describe the formation of amides from terminal nitroalkanes in a two-step, one-pot reaction involving tandem halogenation/umpolung amide synthesis (UmAS).

Graphical abstract: A one-pot amidation of primary nitroalkanes

Supplementary files

Article information

Article type
Communication
Submitted
10 Oct 2015
Accepted
21 Oct 2015
First published
27 Oct 2015
This article is Open Access
Creative Commons BY-NC license

Chem. Commun., 2016,52, 152-155

A one-pot amidation of primary nitroalkanes

K. E. Schwieter and J. N. Johnston, Chem. Commun., 2016, 52, 152 DOI: 10.1039/C5CC08415F

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