Synthesis 1990; 1990(9): 779-781
DOI: 10.1055/s-1990-27012
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.

Stereospecific Synthesis of N-(Diphenylmethylene)-α,β-didehydroamino Acid Methyl Esters from β-Hydroxy-α-amino Acids

Cesarino Balsamini* , Ermanno Duranti, Leonardo Mariani, Americo Salvatori, Gilberto Spadoni
  • *Istituto di Chimica Farmaceutica, Università di Urbino, Piazza del Rinascimento 6, I-61029 Urbino, Italy
Further Information

Publication History

Publication Date:
17 September 2002 (online)

N-(Diphenylmethylene)-α,β-didehydroamino acid methyl esters 2b-d are prepared with absolute geometric selectivity from inexpensive β-hydroxyamino acids through the intermediates N-(diphenylmethylene)- β-hydroxyamino acid methyl esters 1b-d. Besides, an easy conversion from E isomers to the corresponding Z isomers was performed, thus avoiding the use of the uncommon allo-β-hydroxyamino acids as starting materials.

    >