Issue 32, 2012

A simple and efficient method for the facile access of highly functionalized pyridines and their fluorescence property studies

Abstract

In this paper, we have described a simple and convenient method for the one-pot multicomponent reaction of aldehydes, malononitrile and thiols in the presence of a catalytic amount of Bronsted base potassium hydroxide for the efficient synthesis of highly functionalized pyridines. The notable features of this protocol are the simple experimental procedure, short reaction time, broad substrate scope and good yields using a catalytic amount of readily available and cheap base. The photophysical behaviours of the synthesized pyridines have been investigated by UV-Vis and fluorescence spectroscopy and some of the synthesized substituted pyridines exhibit promising fluorescence quantum yields.

Graphical abstract: A simple and efficient method for the facile access of highly functionalized pyridines and their fluorescence property studies

Supplementary files

Article information

Article type
Paper
Submitted
07 Jul 2012
Accepted
09 Oct 2012
First published
31 Oct 2012

RSC Adv., 2012,2, 12305-12314

A simple and efficient method for the facile access of highly functionalized pyridines and their fluorescence property studies

Md. N. Khan, S. Pal, T. Parvin and L. H. Choudhury, RSC Adv., 2012, 2, 12305 DOI: 10.1039/C2RA21385K

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