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.
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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