Rh(iii)-catalyzed tandem oxidative olefination-cyclization of aryl sulfonamides?

RSC Advances Pub Date: 2014-09-26 DOI: 10.1039/C4RA09041A

Abstract

An efficient Rh(III)-catalyzed ortho-selective C–H activation and tandem oxidative olefination-cyclization of aryl sulfonamides is described. The protocol has been applied to various substrates with good functional group tolerance.

Graphical abstract: Rh(iii)-catalyzed tandem oxidative olefination-cyclization of aryl sulfonamides
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