Issue 28, 2010
From the journal:

Chemical Communications

Domino allylic amination/Sonogashira/heterocyclisation reactions: palladium-catalysed three-component synthesis of pyrroles†

Sandrine Lamandé-Langle,a   Mohamed Abarbri,b   Jérôme Thibonnet,b   Alain Duchêne*b  and  Jean-Luc Parrain*c  

* Corresponding authors

a Groupe S.U.C.R.E.S – UMR 7565 Nancy Université – CNRS, BP 70239, F-54506, Nancy Vandoeuvre, France

b Laboratoire de Physicochimie des Matériaux et des Biomolécules, Faculté des Sciences de Tours, EA 4244, Parc de Grandmont, 37200 Tours, France
E-mail: alain.duchêne@univ-tours.fr

c Institut des Sciences Moléculaire de Marseille (ISM2), Equipe STeReO UMR CNRS-6263 Aix-Marseille Université, Campus Scientifique de St Jérôme, 13397 Marseille cedex 20, France
E-mail: jl.parrain@univ-cezanne.fr

Abstract

Three-component reactions with 3,4-diiodoalk-2-enoic derivatives, primary amines, and terminal alkynes proceeded to give trisubstituted pyrroles in fair to good yields in the presence of palladium and copper catalysts under mild reaction conditions.

Graphical abstract: Domino allylic amination/Sonogashira/heterocyclisation reactions: palladium-catalysed three-component synthesis of pyrroles

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/C0CC00500B
Article type
Communication
Submitted
20 Mar 2010
Accepted
13 May 2010
First published
07 Jun 2010

Chem. Commun., 2010,46, 5157-5159

Permissions

Request permissions

Domino allylic amination/Sonogashira/heterocyclisation reactions: palladium-catalysed three-component synthesis of pyrroles

S. Lamandé-Langle, M. Abarbri, J. Thibonnet, A. Duchêne and J. Parrain, Chem. Commun., 2010, 46, 5157 DOI: 10.1039/C0CC00500B

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