Issue 34, 2021

Copper-catalyzed efficient access to 2,4,6-triphenyl pyridines via oxidative decarboxylative coupling of aryl acetic acids with oxime acetates

Abstract

An efficient and concise approach for the synthesis of 2,4,6-triphenyl pyridines has been developed through copper-catalysed oxidative decarboxylative coupling of C(sp3) aryl acetic acids with oxime acetates in DMF at 150 °C under an oxygen atmosphere. Various functional groups were well tolerated and provided the corresponding 2,4,6-triphenyl pyridines in good to excellent yields.

Graphical abstract: Copper-catalyzed efficient access to 2,4,6-triphenyl pyridines via oxidative decarboxylative coupling of aryl acetic acids with oxime acetates

Supplementary files

Article information

Article type
Communication
Submitted
28 Apr 2021
Accepted
16 Jul 2021
First published
22 Jul 2021

New J. Chem., 2021,45, 15205-15209

Copper-catalyzed efficient access to 2,4,6-triphenyl pyridines via oxidative decarboxylative coupling of aryl acetic acids with oxime acetates

B. Varaprasad, K. Bharat Kumar, V. Siddaiah, P. Shyamala and L. Chinnari, New J. Chem., 2021, 45, 15205 DOI: 10.1039/D1NJ01987B

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