Synlett 1998; 1998(10): 1114-1116
DOI: 10.1055/s-1998-1871
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.

Michael Addition Mediated by an Internal Catalyst. A Novel Route to 2-Diethylphosphonoalkanoic Acids

Henryk Krawczyk*
  • *Institute of Organic Chemistry, Technical University (Politechnika), 90-924 Lodz, Zeromskiego 116, Poland; Fax (0-48-42)636-55-30
Further Information

Publication History

Publication Date:
31 December 2000 (online)

Dicyclohexylammonium 2-diethylphosphonoacrylate reacts readily with a variety of 1,3-dicarbonyl and monocarbonyl pronucleophiles to give the corresponding Michael adducts. Self-catalysis in these reactions is postulated.

    >