Issue 17, 2015

Au-catalyzed ring-opening reactions of 2-(1-alkynyl-cyclopropyl)pyridines with nucleophiles

Abstract

A novel method for the C–C bond cleavage of cyclopropanes was developed by gold-catalyzed cycloisomerization of 2-(1-alkynyl-cyclopropyl)pyridine with nucleophiles, which provides efficient access to structurally diverse indolizines under mild conditions. A series of N-, C- and O-based nucleophiles were involved in this reaction to afford the corresponding indolizines in modest to excellent yields.

Graphical abstract: Au-catalyzed ring-opening reactions of 2-(1-alkynyl-cyclopropyl)pyridines with nucleophiles

Supplementary files

Article information

Article type
Communication
Submitted
16 Mar 2015
Accepted
20 Mar 2015
First published
23 Mar 2015

Org. Biomol. Chem., 2015,13, 4855-4858

Au-catalyzed ring-opening reactions of 2-(1-alkynyl-cyclopropyl)pyridines with nucleophiles

R. Liu, S. Ye, C. Lu, B. Xiang, J. Gao and Y. Jia, Org. Biomol. Chem., 2015, 13, 4855 DOI: 10.1039/C5OB00523J

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