Issue 23, 2006
From the journal:

Organic & Biomolecular Chemistry

Efficient Friedel–Crafts alkylation of indoles and pyrrole with enones and nitroalkene in water†

Najmedin Azizi,*b   Fezzeh Arynasaba  and  Mohammad R. Saidi*a  

* Corresponding authors

a Department of Chemistry, Sharif University of Technology, P. O. Box 11465-9516, Tehran, Iran
E-mail: Saidi@sharif.edu
Fax: +98 (0)21 66005718

b Organic Chemistry Laboratory, Chemistry & Chemical Engineering Research Center of Iran, P.O. Box 14335-186, Tehran, Iran

Abstract

An operationally simple and entirely green protocol for heteropoly acid (10 mg) catalyst conjugate addition of indoles and pyrrole to unsaturated carbonyl compounds and nitroalkene in water at ambient temperature in good to excellent yields has been developed.

Graphical abstract: Efficient Friedel–Crafts alkylation of indoles and pyrrole with enones and nitroalkene in water

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/B610263H
Article type
Communication
Submitted
18 Jul 2006
Accepted
06 Oct 2006
First published
17 Oct 2006

Org. Biomol. Chem., 2006,4, 4275-4277

Permissions

Request permissions

Efficient Friedel–Crafts alkylation of indoles and pyrrole with enones and nitroalkene in water

N. Azizi, F. Arynasab and M. R. Saidi, Org. Biomol. Chem., 2006, 4, 4275 DOI: 10.1039/B610263H

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