Issue 39, 2013

Cobalt-catalyzed oxidative [3 + 2] cycloaddition reactions: an efficient synthesis of pyrrolo- and imidazo-[2,1-a]isoquinolines

Abstract

A cobalt-catalyzed oxidative [3 + 2] cycloaddition cascades of dihydroisoquinoline esters with nitroolefins or N-sulfuryl aldimines were developed at room temperature. A multi-component reaction for the synthesis of 5,6-dihydroimidazo[2,1-a]isoquinolines were also realized under almost identical conditions. This method is particularly suitable for the synthesis of tricyclic nitrogen heterocycles due to its simple manipulation, wide scope of the reaction substrates and excellent regioselectivity.

Graphical abstract: Cobalt-catalyzed oxidative [3 + 2] cycloaddition reactions: an efficient synthesis of pyrrolo- and imidazo-[2,1-a]isoquinolines

Supplementary files

Article information

Article type
Communication
Submitted
11 Jul 2013
Accepted
10 Aug 2013
First published
14 Aug 2013

Org. Biomol. Chem., 2013,11, 6691-6694

Cobalt-catalyzed oxidative [3 + 2] cycloaddition reactions: an efficient synthesis of pyrrolo- and imidazo-[2,1-a]isoquinolines

C. Feng, J. Su, Y. Yan, F. Guo and Z. Wang, Org. Biomol. Chem., 2013, 11, 6691 DOI: 10.1039/C3OB41424H

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