Issue 6, 2012

Cu(0) nanoparticle catalyzed efficient reductive cleavage of isoxazoline, carbonyl azide and domino cyclization in water medium

Abstract

Small Cu(0)-nanoparticles (NPs) are fabricated utilizing CuSO4·5H2O, surfactant (SDS) and ascorbic acid in aqueous medium. Its outstanding catalytic activity under low catalyst loading is developed toward reductive cleavage of isoxazoline, carbonyl azide and domino cyclization to furnish valuable 2-hydroxy-4-keto esters, primary amides and a new class of heterocycle, 4-hydroxy-2-pyrroline-5-one.

Graphical abstract: Cu(0) nanoparticle catalyzed efficient reductive cleavage of isoxazoline, carbonyl azide and domino cyclization in water medium

Supplementary files

Article information

Article type
Communication
Submitted
20 Feb 2012
Accepted
30 Mar 2012
First published
24 Apr 2012

Green Chem., 2012,14, 1589-1592

Cu(0) nanoparticle catalyzed efficient reductive cleavage of isoxazoline, carbonyl azide and domino cyclization in water medium

K. S. Gayen, T. Sengupta, Y. Saima, A. Das, D. K. Maiti and A. Mitra, Green Chem., 2012, 14, 1589 DOI: 10.1039/C2GC35252D

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