Issue 29, 2015

Pd-catalyzed dehydrogenative C–H activation of iminyl hydrogen with the indole C3–H and C2–H bond: an elegant synthesis of indeno[1,2-b]indoles and indolo[1,2-a]indoles

Abstract

Two Pd(OAc)2-catalyzed sequential C–H activations (C2–H arylation followed by indole C3–H activation with iminyl hydrogen) were employed for the synthesis of indeno[1,2-b]indoles in one pot. This procedure describes a simple way of introducing substituent diversity into this highly important core structure. Indole C2–H activation was also achieved for the synthesis of indolo[1,2-a]indoles.

Graphical abstract: Pd-catalyzed dehydrogenative C–H activation of iminyl hydrogen with the indole C3–H and C2–H bond: an elegant synthesis of indeno[1,2-b]indoles and indolo[1,2-a]indoles

Supplementary files

Article information

Article type
Paper
Submitted
18 Dec 2014
Accepted
19 Feb 2015
First published
20 Feb 2015

RSC Adv., 2015,5, 22480-22489

Author version available

Pd-catalyzed dehydrogenative C–H activation of iminyl hydrogen with the indole C3–H and C2–H bond: an elegant synthesis of indeno[1,2-b]indoles and indolo[1,2-a]indoles

S. Hazra, B. Mondal, R. N. De and B. Roy, RSC Adv., 2015, 5, 22480 DOI: 10.1039/C4RA16661B

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