Issue 2, 2016

Rapid access to bicyclic δ-lactones via carbene-catalyzed activation and cascade reaction of unsaturated carboxylic esters

Abstract

Carboxylic esters are an excellent choice of substrates in organic synthesis. Here we demonstrate that carbene-catalyzed activation of α,β-unsaturated ester can be developed to synthesize sophisticated multi-cyclic molecules in a single step cascade process. The iridoid-type lactone products are obtained with high stereo-selectivities, and can readily undergo further transformations.

Graphical abstract: Rapid access to bicyclic δ-lactones via carbene-catalyzed activation and cascade reaction of unsaturated carboxylic esters

Supplementary files

Article information

Article type
Research Article
Submitted
04 Nov 2015
Accepted
03 Dec 2015
First published
03 Dec 2015

Org. Chem. Front., 2016,3, 145-149

Author version available

Rapid access to bicyclic δ-lactones via carbene-catalyzed activation and cascade reaction of unsaturated carboxylic esters

Z. Fu, X. Wu and Y. R. Chi, Org. Chem. Front., 2016, 3, 145 DOI: 10.1039/C5QO00348B

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