Issue 21, 2010

Synthesis of new pentacyclic chromophores through a highly regio- and diastereoselective cascade process

Abstract

A new family of pentacyclic compounds incorporating a central 1,2-dihydropyridine core is obtained through a pseudo three-component reaction. Four new bonds and two stereocenters with trans relationship are produced during the cascade process under palladium catalysis.

Graphical abstract: Synthesis of new pentacyclic chromophores through a highly regio- and diastereoselective cascade process

Supplementary files

Article information

Article type
Communication
Submitted
06 Jul 2010
Accepted
02 Sep 2010
First published
16 Sep 2010

Org. Biomol. Chem., 2010,8, 4815-4818

Synthesis of new pentacyclic chromophores through a highly regio- and diastereoselective cascade process

Z. E. A. Chamas, O. Dietz, E. Aubert, Y. Fort and V. Mamane, Org. Biomol. Chem., 2010, 8, 4815 DOI: 10.1039/C0OB00390E

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