Issue 48, 2016, Issue in Progress

Recent developments in multicomponent synthesis of structurally diversified tetrahydropyridines

Abstract

Tetrahydropyridines (THPDs) have been recognized as a major constituent of naturally occurring alkaloids. Being heterocyclic nitrogenous compounds, they therefore display robust biological and pharmacological profiles. In this context, they are fascinating synthetic targets in synthetic chemistry and as a consequence of this their synthesis through simple and convenient tactics has emerged as an important and challenging task. To meet such challenge, multicomponent reactions (MCRs) are employed as an excellent tool for achieving compounds containing complex diversity in single step and production of their vast libraries. This review represents the advancement made in the field of multicomponent synthesis of THPDs and their derivatives of the last few years.

Graphical abstract: Recent developments in multicomponent synthesis of structurally diversified tetrahydropyridines

Article information

Article type
Review Article
Submitted
14 Mar 2016
Accepted
11 Apr 2016
First published
27 Apr 2016

RSC Adv., 2016,6, 42045-42061

Recent developments in multicomponent synthesis of structurally diversified tetrahydropyridines

Md. M. Khan, S. Khan, Saigal and S. Iqbal, RSC Adv., 2016, 6, 42045 DOI: 10.1039/C6RA06767K

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