Synlett 2012; 23(9): 1309-1314
DOI: 10.1055/s-0031-1290918
letter
© Georg Thieme Verlag Stuttgart · New York

A Reusable TNF-Tagged Chiral Bis(oxazoline)–Copper Catalyst for Diels– Alder Transformations

Dorian Didier
a   Equipe de Catalyse Moléculaire, Univ Paris-Sud, ICMMO, UMR 8182, Orsay 91405, France
,
Emmanuelle Schulz*
a   Equipe de Catalyse Moléculaire, Univ Paris-Sud, ICMMO, UMR 8182, Orsay 91405, France
b   CNRS, Orsay 91405, France, Fax: +33(1)69154680   Email: emmanuelle.schulz@u-psud.fr
› Author Affiliations
Further Information

Publication History

Received: 09 January 2012

Accepted after revision: 06 March 2012

Publication Date:
26 April 2012 (online)


Abstract

A chiral bis(oxazoline) ligand, substituted on the methylene bridge by a covalent link to an electron-deficient moiety (2,4,7-trinitrofluoren-9-one, TNF), is a useful ligand associated to copper(II) salts to promote enantioselective Diels–Alder reactions between N-acyloxazolidinones and cyclopentadiene. Owing to different solubility properties, the corresponding catalyst was precipitated by pentane addition after reaction completion and was easily recovered by filtration. It was successfully reused in up to 20 successive catalytic cycles for the formation of the targeted products with no loss of either the activity or the enantioselectivity along with the recycling.