Issue 11, 2017

Pd-Catalyzed oxidative annulation of enamides with diazabicyclic olefins: rapid access to cyclopentene fused 2-pyrrolines

Abstract

An efficient stereoselective route for the synthesis of cyclopentene fused 2-pyrrolines has been established via a Pd-catalyzed C–H activation/oxidative coupling of aryl enamides with diazabicyclic olefins. The proposed two-stage mechanism was successfully proven by isolating the intermediate trans-disubstituted cyclopentene.

Graphical abstract: Pd-Catalyzed oxidative annulation of enamides with diazabicyclic olefins: rapid access to cyclopentene fused 2-pyrrolines

Supplementary files

Article information

Article type
Communication
Submitted
01 Nov 2016
Accepted
30 Nov 2016
First published
30 Nov 2016

Chem. Commun., 2017,53, 1848-1851

Pd-Catalyzed oxidative annulation of enamides with diazabicyclic olefins: rapid access to cyclopentene fused 2-pyrrolines

P. V. Santhini, G. Nimisha, J. John, E. Suresh, R. L. Varma and K. V. Radhakrishnan, Chem. Commun., 2017, 53, 1848 DOI: 10.1039/C6CC08753A

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