Issue 73, 2015

A gold-catalyzed 1,2-acyloxy migration/intramolecular cyclopropanation/ring enlargement cascade: syntheses of medium-sized heterocycles

Abstract

The synthesis of medium-sized heterocycles possessing a trans double bond is still a challenge. Herein, gold(I)-catalyzed 1,2-acyloxy migration/intramolecular cyclopropanation/ring enlargement cascade reaction of furans has been developed, providing highly efficient access to ten- and eleven-membered heterocycles with a broad substrate scope under mild reaction conditions. The reaction outcome features high chemoselectivity at the C5-position of furan. Moreover, a trans-double bond was embodied in the medium ring system.

Graphical abstract: A gold-catalyzed 1,2-acyloxy migration/intramolecular cyclopropanation/ring enlargement cascade: syntheses of medium-sized heterocycles

Supplementary files

Article information

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

Chem. Commun., 2015,51, 13937-13940

Author version available

A gold-catalyzed 1,2-acyloxy migration/intramolecular cyclopropanation/ring enlargement cascade: syntheses of medium-sized heterocycles

Y. Sun, X. Tang and M. Shi, Chem. Commun., 2015, 51, 13937 DOI: 10.1039/C5CC05808B

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