Issue 5, 2010

Scandium triflate-catalyzed one-pot domino approach towards general and efficient syntheses of unsymmetrical 9-substituted xanthene derivatives

Abstract

A general and efficient one-pot cascade/tandem approach to synthesize unsymmetrical 9-aryl/heteroaryl xanthenes has been developed under extremely mild reaction conditions using 10 mol% Sc(OTf)3 as a catalyst. This strategy has been further extended to synthesize 9-(thioaryl) xanthenes through tandem carbonsulfur (C–S) and carboncarbon (C–C) bond formation. Novel C–C and C–S bond cleavage promoted by Sc(OTf)3 is also discussed during mechanistic investigation.

Graphical abstract: Scandium triflate-catalyzed one-pot domino approach towards general and efficient syntheses of unsymmetrical 9-substituted xanthene derivatives

Supplementary files

Article information

Article type
Paper
Submitted
21 Sep 2009
Accepted
18 Nov 2009
First published
06 Jan 2010

Org. Biomol. Chem., 2010,8, 1097-1105

Scandium triflate-catalyzed one-pot domino approach towards general and efficient syntheses of unsymmetrical 9-substituted xanthene derivatives

R. Singh and G. Panda, Org. Biomol. Chem., 2010, 8, 1097 DOI: 10.1039/B919666H

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