Issue 93, 2014

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

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

Supplementary files

Article information

Article type
Paper
Submitted
21 Aug 2014
Accepted
26 Sep 2014
First published
26 Sep 2014

RSC Adv., 2014,4, 51309-51314

Author version available

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

Q. Ding, T. Liu, Q. Zheng, Y. Zhang, L. Long and Y. Peng, RSC Adv., 2014, 4, 51309 DOI: 10.1039/C4RA09041A

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