Issue 104, 2014

A Cu-catalysed synthesis of substituted 3-methyleneisoindolin-1-one

Abstract

A Cu(I)-catalysed synthesis of substituted 3-methyleneisoindolin-1-ones using alkynyl acids as an alkyne source has been developed. The reaction involves the decarboxylative cross-coupling of 2-halobenzamides with aryl alkynyl acids, followed by 5-exo-dig heteroannulation. While reactions of 2-iodo benzamides proceeded without a ligand, for 2-bromo substrates, the assistance of a ligand is essential.

Graphical abstract: A Cu-catalysed synthesis of substituted 3-methyleneisoindolin-1-one

Supplementary files

Article information

Article type
Paper
Submitted
20 Oct 2014
Accepted
27 Oct 2014
First published
03 Nov 2014

RSC Adv., 2014,4, 59902-59907

Author version available

A Cu-catalysed synthesis of substituted 3-methyleneisoindolin-1-one

A. Gogoi, S. Guin, S. K. Rout, G. Majji and B. K. Patel, RSC Adv., 2014, 4, 59902 DOI: 10.1039/C4RA12782J

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