Issue 23, 2013

Propargyl vinyl ethers as heteroatom-tethered enyne surrogates: diversity-oriented strategies for heterocycle synthesis

Abstract

This article presents recent progress in the conversion of propargyl vinyl ethers into heterocyclic scaffolds and how this goal can be reached in a diversity-oriented approach. The article also includes examples of transformations of propargyl vinyl ethers where the propargyl vinyl ether moieties are formed in situ. Furthermore, related reactions transforming propargyl vinyl amines to heterocycles are discussed.

Graphical abstract: Propargyl vinyl ethers as heteroatom-tethered enyne surrogates: diversity-oriented strategies for heterocycle synthesis

Article information

Article type
Feature Article
Submitted
04 Oct 2012
Accepted
08 Jan 2013
First published
08 Jan 2013

Chem. Commun., 2013,49, 2272-2283

Propargyl vinyl ethers as heteroatom-tethered enyne surrogates: diversity-oriented strategies for heterocycle synthesis

Z. Zhu and S. F. Kirsch, Chem. Commun., 2013, 49, 2272 DOI: 10.1039/C3CC37258H

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