Copper(ii)-mediated, carbon degradation-based amidation of phenylacetic acids toward N-substituted benzamides†
Leiling Deng,Bin Huang,Yunyun Liu
Organic & Biomolecular Chemistry Pub Date : 02/02/2018 00:00:00 , DOI:10.1039/C8OB00064F
Abstract

The unprecedented synthesis of N-aryl substituted benzamides via the assembly of primary amines and phenylacetic acids has been developed in the presence of copper(II) acetate. This tandem transformation involving carbon–carbon bond cleavage provides a complementary tool with particular application in the synthesis of secondary benzamides.

Graphical abstract: Copper(ii)-mediated, carbon degradation-based amidation of phenylacetic acids toward N-substituted benzamides