Issue 1, 2015

Copper-catalyzed regioselective synthesis of furan via tandem cycloaddition of ketone with an unsaturated carboxylic acid under air

Abstract

A catalytic decarboxylative annulation has been developed for the regioselective synthesis of trisubstituted furans by the cycloaddition of ketones with α,β-unsaturated carboxylic acids under ambient air. A library of furan derivatives were obtained in good yields from the readily available substrates in the combination of a catalytic amount of Cu-salt and a stoichiometric amount of water. Water plays a crucial role in this catalytic transformation.

Graphical abstract: Copper-catalyzed regioselective synthesis of furan via tandem cycloaddition of ketone with an unsaturated carboxylic acid under air

Supplementary files

Article information

Article type
Paper
Submitted
25 Jun 2014
Accepted
20 Oct 2014
First published
20 Oct 2014

Org. Biomol. Chem., 2015,13, 309-314

Copper-catalyzed regioselective synthesis of furan via tandem cycloaddition of ketone with an unsaturated carboxylic acid under air

M. Ghosh, S. Mishra, K. Monir and A. Hajra, Org. Biomol. Chem., 2015, 13, 309 DOI: 10.1039/C4OB01320D

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