Synthesis 1990; 1990(2): 132-134
DOI: 10.1055/s-1990-26810
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.

Phosphoranaloge von Aminosäuren III1. Synthese optisch aktiver 1-Aminoalkylphosphonsäuren der (S)- und (R)-Reihe mit Hilfe von (-)-Ephedrin als Auxiliar

Michael Sting* , Wolfgang Steglich
  • *Institut für Organische Chemie and Biochemie der Universität Bonn, Gerhard-Domagk-Straße 1, D-5300 Bonn 1, Federal Republic of Germany
Further Information

Publication History

Publication Date:
17 September 2002 (online)

Synthesis of Optically Active (S)- and (R)-1-Aminoalkylphosphonic Acids Using (-)-Ephedrine as Auxiliary The 2-benzoylaminomethyl-3,4-dimethyl-2-oxo-5-phenyl-2λ5-1, 3,2-oxazaphospholidines 2 and 2′, epimeric at the 2-position, are easily obtainable from benzoylaminomethylphosphonic acid dichloride (1) and (-)-ephedrine and are diastereoselectively alkylated at the P-C-N methylene group to yield compounds 3 and 3′, respectively. Hydrolysis of these products affords 1-aminoalkylphosphonic acids 4 and 4′, with (S)- and (R)-configuration, respectively.

    >