Synthesis 2005(12): 2084-2089  
DOI: 10.1055/s-2005-869972
PSP
© Georg Thieme Verlag Stuttgart · New York

Efficient One-Pot Synthesis of Substituted 1-Acylaminocyclohex-2-enes

Sandra Hübner, Helfried Neumann, Axel Jacobi Wangelin, Stefan Klaus, Dirk Strübing, Holger Klein, Matthias Beller*
Leibniz-Institut für Organische Katalyse an der Universität Rostock e.V., Albert-Einstein-Str. 29a, 18059 Rostock, Germany
Fax: +49(381)4669324; e-Mail: matthias.beller@ifok.uni-rostock.de;
Further Information

Publication History

Received 14 January 2005
Publication Date:
06 June 2005 (online)

Abstract

Substituted 1-acylaminocyclohex-2-enes can be prepared in good to excellent yields by multicomponent reactions (MCR) utilizing ubiquitously available aldehydes, amides, and dienophiles (AAD reaction). This novel one-pot reaction involves 1-acylaminobuta-1,3-dienes as key intermediates, which undergo subsequent Diels-Alder reactions.