Synlett 1998; 1998(8): 843-844
DOI: 10.1055/s-1998-1793
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.

Highly syn-Diastereoselective Synthesis of NH-3-Benzyloxy-4-aryl-azetidin-2-ones via a Two-Step Staudinger Reaction

Sergio Bacchi* , Alessandro Bongini, Mauro Panunzio, Marzia Villa
  • *CSFM-C.N.R. and University of Bologna, Dipartimento di Chimica "G. Ciamician", Via Selmi 2, 40126 Bologna, Italy; Fax + 39-51-25 94 56; E-mail: panunzio@ciam.unibo.it
Further Information

Publication History

Publication Date:
31 December 2000 (online)

New conditions for the Staudinger reaction provide NH-3-benzyloxy-4-aryl-β-lactams in good yields with complete cis-diastereoselectivity.