Issue 13, 2021

Transition-metal-free decarboxylative ipso amination of aryl carboxylic acids

Abstract

A convenient DMAP-catalysed decarboxylative amination of aryl and alkyl carboxylic acids is developed under transition-metal-free conditions. This reaction allows the sustainable synthesis of a wide range of aryl and alkyl amines in useful to good yields, avoiding the use of any activating reagent, transition-metal catalyst and external oxidant. The late-stage modification of bioactive acids and concise synthesis of carbamate and ureas demonstrated the synthetic potential of this methodology.

Graphical abstract: Transition-metal-free decarboxylative ipso amination of aryl carboxylic acids

Supplementary files

Article information

Article type
Research Article
Submitted
20 Mar 2021
Accepted
27 Apr 2021
First published
27 Apr 2021

Org. Chem. Front., 2021,8, 3434-3439

Transition-metal-free decarboxylative ipso amination of aryl carboxylic acids

J. Zhang, Y. Hou, Y. Tang, J. Xu, Z. Liu, Y. Gao and X. Hu, Org. Chem. Front., 2021, 8, 3434 DOI: 10.1039/D1QO00442E

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