Synthesis 1986; 1986(8): 683-686
DOI: 10.1055/s-1986-31750
communication
© 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.

A New Approach to the Synthesis of Pyrrolizines: A One-pot Procedure from 2H-Pyrroles

P. F. Belloir* , A. Laurent, P. Mison, S. Lesniak, R. Bartnik
  • *Universite Claude Bernard-Lyon 1, Laboratoire de Chimie Organique III. U. A. CNRS 0467, 43, Bd. du 11 Novembre 1918, F-6922 Villeurbanne Cedex, France
Further Information

Publication History

Publication Date:
22 August 2002 (online)

A convenient method for synthesis of the pyrrolizine nucleus is reported. The pyrrolizines were obtained through 1,3-dipolar cycloaddition on azomethine ylids 4 generated in situ from 2H-pyrroles. The new adducts were characterized by 1H- and 13C-N.M.R. data as well as mass spectrometry.

    >