Issue 10, 2005
From the journal:

Chemical Communications

1-Triflylpyrroles as efficient dienophiles in normal electron demand [4+2] cycloaddition reactions under pressure†

Antony Chrétien,a   Isabelle Chataignera  and  Serge R. Piettre*a  

* Corresponding authors

a Laboratoire des Fonctions Azotées et Oxygénées Complexes, Université de Rouen, UMR CNRS 6014, IRCOF, Rue Tesnières, F-76821 Mont Saint Aignan, France
E-mail: Serge.Piettre@univ-rouen.fr
Fax: +33 23552 2971
Tel: +33 23552 2970

Abstract

1-Triflylpyrroles bearing acetyl group(s) on position 3, or 2 and 4, are efficient dienophiles in normal electron demand Diels–Alder reactions activated by high pressures and Lewis acids.

Graphical abstract: 1-Triflylpyrroles as efficient dienophiles in normal electron demand [4+2] cycloaddition reactions under pressure

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Article information

DOI
https://doi.org/10.1039/B414978E
Article type
Communication
Submitted
28 Sep 2004
Accepted
01 Dec 2004
First published
21 Jan 2005

Chem. Commun., 2005, 1351-1353

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1-Triflylpyrroles as efficient dienophiles in normal electron demand [4+2] cycloaddition reactions under pressure

A. Chrétien, I. Chataigner and S. R. Piettre, Chem. Commun., 2005, 1351 DOI: 10.1039/B414978E

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