Issue 81, 2017

C(sp3)–H amination of 8-methylquinolines with azodicarboxylates under Rh(iii) catalysis: cytotoxic evaluation of quinolin-8-ylmethanamines

Abstract

The rhodium(III)-catalyzed C(sp3)–H amination reaction of 8-methylquinolines and azodicarboxylates is described. A cationic rhodium catalyst in the presence of lithium acetate and lithium carbonate was found to be an optimal catalytic system for the construction of quinolin-8-ylmethanamine derivatives, which were evaluated for in vitro cytotoxicity against human breast adenocarcinoma cells (MCF-7) and human prostate adenocarcinoma cells (LNCaP).

Graphical abstract: C(sp3)–H amination of 8-methylquinolines with azodicarboxylates under Rh(iii) catalysis: cytotoxic evaluation of quinolin-8-ylmethanamines

Supplementary files

Article information

Article type
Communication
Submitted
25 Aug 2017
Accepted
21 Sep 2017
First published
21 Sep 2017

Chem. Commun., 2017,53, 11197-11200

C(sp3)–H amination of 8-methylquinolines with azodicarboxylates under Rh(III) catalysis: cytotoxic evaluation of quinolin-8-ylmethanamines

T. Jeong, N. K. Mishra, P. Dey, H. Oh, S. Han, S. H. Lee, H. S. Kim, J. Park and I. S. Kim, Chem. Commun., 2017, 53, 11197 DOI: 10.1039/C7CC06670H

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