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Centre de Recherche de Gif, Institut de Chimie des Substances Naturelles, CNRS, 91198 Gif-sur-Yvette Cedex, France
E-mail: masson@icsn.cnrs-gif.fr
; Fax: +33 1 69077247
Chem. Soc. Rev., 2013,42, 902-923
DOI:
10.1039/C2CS35370A
Received
04 Sep 2012,
First published online
21 Nov 2012
The aza-Diels Alder reaction has become one of the most widely used synthetic tools for the preparation of N-containing 6-membered heterocycles. Numerous important developments have been reported to render this reaction catalytic and enantioselective. This tutorial review highlights strategies and recent advances to achieve high efficiency and selectivity through the use of organocatalysts and transition metal complexes, allowing also the extension of this transformation substrate scope.
A review, with 55 references, of the use of metal complexes and organocatalysts in Diels–Alder reactions for the efficient and/or enantioselective preparation of aza-heterocycles.
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