Synthesis 1987; 1987(12): 1055-1057
DOI: 10.1055/s-1987-28168
paper
© 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.

The Synthesis of 4-Oxo-2-pentenoic Esters by Wittig Reaction Using α-Oxoesters

Paul Francis Schuda* , Cynthia B. Ebner, Steven J. Potlock
  • *Department of Chemistry, University of Maryland, College Park, MD 20742, U.S.A.
Further Information

Publication History

Publication Date:
20 August 2002 (online)

The reaction of stabilized ylides with α-oxoesters gives high yields of 4-oxo-2-pentenoic esters. By suitable substitution of each reactant, highly substituted and hindered enones can be prepared in quantity, with excellent geometric selectivity.

    >