Issue 11, 2015

Bi(OTf)3-catalyzed C–H bond functionalization of azaarenes for the facile access to oxindoles featuring quaternary carbon centers

Abstract

The direct sp3 C–H bond functionalization of 2-alkyl azaarenes to isatylidene malononitriles has been achieved using Bi(OTf)3 as the catalyst, resulting in a series of oxindoles containing an all-carbon quaternary center in moderate to good yields. This protocol provided an efficient and convenient method for the construction of potentially useful azaarene substituted oxindoles.

Graphical abstract: Bi(OTf)3-catalyzed C–H bond functionalization of azaarenes for the facile access to oxindoles featuring quaternary carbon centers

Supplementary files

Article information

Article type
Communication
Submitted
09 Nov 2014
Accepted
10 Dec 2014
First published
15 Dec 2014

RSC Adv., 2015,5, 8285-8288

Bi(OTf)3-catalyzed C–H bond functionalization of azaarenes for the facile access to oxindoles featuring quaternary carbon centers

B. Lu, Q. Lu, S. Zhuang, J. Cheng and B. Huang, RSC Adv., 2015, 5, 8285 DOI: 10.1039/C4RA14144J

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