Issue 41, 2016, Issue in Progress

tert-Butyl nitrite mediated azo coupling between anilines and imidazoheterocycles

Abstract

A tBuONO mediated practical and efficient method for the synthesis of azo imidazoheterocycles with broad functionalities has been achieved by the reaction between imidazoheterocycles and anilines at room temperature in goods yields. Azo indolizines were also prepared by employing this methodology. Mild reaction conditions, tolerance of wide functionalities, operational simplicity and easy purification of the products are the notable advantages of the current protocol.

Graphical abstract: tert-Butyl nitrite mediated azo coupling between anilines and imidazoheterocycles

Supplementary files

Article information

Article type
Paper
Submitted
02 Feb 2016
Accepted
29 Mar 2016
First published
30 Mar 2016

RSC Adv., 2016,6, 34146-34152

tert-Butyl nitrite mediated azo coupling between anilines and imidazoheterocycles

A. Chakraborty, S. Jana, G. Kibriya, A. Dey and A. Hajra, RSC Adv., 2016, 6, 34146 DOI: 10.1039/C6RA03070J

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