Issue 72, 2015

Palladium(ii)-catalysed regioselective synthesis of 3,4-disubstituted quinolines and 2,3,5-trisubstituted pyrroles from alkenes via anti-Markovnikov selectivity

Abstract

A novel strategy has been identified for the regioselective synthesis of 3,4-disubstituted quinolines and 2,3,5-trisubstituted pyrroles from simple alkenes via anti-Markovnikov selectivity under palladium catalysis. The salient features are synthesis of two different heterocycles, readily available starting materials, broad substrate scope, moderate to good yields and use of molecular oxygen as a terminal oxidant.

Graphical abstract: Palladium(ii)-catalysed regioselective synthesis of 3,4-disubstituted quinolines and 2,3,5-trisubstituted pyrroles from alkenes via anti-Markovnikov selectivity

Supplementary files

Article information

Article type
Communication
Submitted
24 Jun 2015
Accepted
24 Jul 2015
First published
24 Jul 2015

Chem. Commun., 2015,51, 13795-13798

Author version available

Palladium(II)-catalysed regioselective synthesis of 3,4-disubstituted quinolines and 2,3,5-trisubstituted pyrroles from alkenes via anti-Markovnikov selectivity

G. C. Senadi, W. Hu, A. M. Garkhedkar, S. S. K. Boominathan and J. Wang, Chem. Commun., 2015, 51, 13795 DOI: 10.1039/C5CC05196G

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