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

dc.contributor.author	Roberto Ballini
dc.contributor.author	Giovanna Bosica
dc.contributor.author	Dennis Fiorini
dc.date.accessioned	2012-11-20T13:57:39Z
dc.date.accessioned	2025-02-17T14:02:13Z
dc.date.available	2012-11-20T13:57:39Z
dc.date.issued	2012-11-20
dc.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	en_US
dc.description.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	en_US
dc.identifier.uri	https://dl.ftveti.edu.et/handle/123456789/4237
dc.language.iso	en	en_US
dc.subject	Uncatalyzed conversion of linear a-nitro ketones into amides by reaction with primary amines under solventless conditions	en_US
dc.title	Uncatalyzed conversion of linear a-nitro ketones into amides by reaction with primary amines under solventless conditions	en_US
dc.type	Article	en_US

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