Synlett 2001; 2001(9): 1437-1439
DOI: 10.1055/s-2001-16772
letter
© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. This journal, including all individual contributions and illustrations published therein, is legally protected by copyright for the duration of the copyright period. Any use, exploitation or commercialization outside the narrow limits set by copyright legislation, without the publisher's consent, is illegal and liable to criminal prosecution. This applies in particular to photostat reproduction, copying, cyclostyling, mimeographing or duplication of any kind, translating, preparation of microfilms, and electronic data processing and storage.

Regio- and Diastereoselective Synthesis of N-Aryl-5-alkylidene-5H-pyrrol-2-ones by a new Domino Reaction of 1,3-Dicarbonyl Dianions with Oxalic Acid-bis(imidoyl)chlorides

Peter Langer* , Manfred Döring
  • *Institut für Organische Chemie der Georg-August-Universität Göttingen, Tammannstrasse 2, 37077 Göttingen, Germany
Further Information

Publication History

Publication Date:
28 August 2001 (online)

The reaction of dilithiated dicarbonyl compounds with oxalic acid-bis(imidoyl)chlorides results in regio- and stereoselective formation of 5-(alkylidene)-5H-pyrrol-2-ones.

    >