Issue 4, 2011

Transition metal mediated construction of pyrrole ring on 2,3-dihydroquinolin-4(1H)-one: synthesis and pharmacological evaluation of novel tricyclic heteroarenes

Abstract

A facile two-step method for the construction of fused pyrrole ring leading to 5-substituted 2,3-dihydro-1H-pyrrolo[3,2,1-ij]quinolin-1-ones via C–C followed by intramolecular C–N bond forming reaction is described. In vitro pharmacological evaluation and molecular modelling studies of some of the compounds synthesized are presented.

Graphical abstract: Transition metal mediated construction of pyrrole ring on 2,3-dihydroquinolin-4(1H)-one: synthesis and pharmacological evaluation of novel tricyclic heteroarenes

Supplementary files

Article information

Article type
Communication
Submitted
23 Sep 2010
Accepted
03 Dec 2010
First published
06 Dec 2010

Org. Biomol. Chem., 2011,9, 1004-1007

Transition metal mediated construction of pyrrole ring on 2,3-dihydroquinolin-4(1H)-one: synthesis and pharmacological evaluation of novel tricyclic heteroarenes

M. Layek, A. Reddy M., A. V. Dhanunjaya Rao, M. Alvala, M. K. Arunasree, A. Islam, K. Mukkanti, J. Iqbal and M. Pal, Org. Biomol. Chem., 2011, 9, 1004 DOI: 10.1039/C0OB00771D

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