Issue 16, 2018

Ene cyclization reaction in heterocycle synthesis

Abstract

The ene cyclization has evolved to become an indispensable tool for the synthesis of various ring size heterocyclic compounds. In the past and recent years, many exciting reports have demonstrated the broad scope and synthetic utility of ene cyclization and the versatility of oxonium ion, iminium ion and thionium ion intermediates. Moreover, the ease of regio- and stereoselectivity of ene cyclization has led to the development of new types of heterocyclic compounds. This article aims at reviewing the utilities of ene cyclization reactions for the synthesis of various ring sizes of oxygen, nitrogen and sulfur heterocycles. It also covers some applications in natural product synthesis. The mechanism of the reactions is discussed wherever necessary. The review article covers the time period from 1986 to 2017.

Graphical abstract: Ene cyclization reaction in heterocycle synthesis

Article information

Article type
Review Article
Submitted
19 Feb 2018
Accepted
20 Mar 2018
First published
20 Mar 2018

Org. Biomol. Chem., 2018,16, 2820-2840

Ene cyclization reaction in heterocycle synthesis

P. Saha and A. K. Saikia, Org. Biomol. Chem., 2018, 16, 2820 DOI: 10.1039/C8OB00429C

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements