Uncatalyzed conversion of linear a-nitro ketones into amides by reaction with primary amines under solventless conditions

Thumbnail Image

Date

2012-11-20

Journal Title

Journal ISSN

Volume Title

Publisher

Abstract

The reaction of linear a-nitro ketones with primary amines allows the formation of amides through the cleavage of the carbon– carbon bond between the carbonyl group and the carbon-nitro group moiety, promoted by the nucleophilic effect of the amine. The reaction is performed at room temperature, without any catalyst and/or solvent. q 2003 Elsevier Science Ltd. All rights reserved

Description

The reaction of linear a-nitro ketones with primary amines allows the formation of amides through the cleavage of the carbon– carbon bond between the carbonyl group and the carbon-nitro group moiety, promoted by the nucleophilic effect of the amine. The reaction is performed at room temperature, without any catalyst and/or solvent. q 2003 Elsevier Science Ltd. All rights reserved

Keywords

Uncatalyzed conversion of linear a-nitro ketones into amides by reaction with primary amines under solventless conditions

Citation

Endorsement

Review

Supplemented By

Referenced By