Synlett 2000; 2000(7): 1046-1048
DOI: 10.1055/s-2000-6680
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.

Facile Synthesis of 3,4-Dihydroxyprolines as an Application of the l-Threonine Aldolase-Catalyzed Aldol Reaction

Mikio Fujii* , Tsuyoshi Miura, Tetsuya Kajimoto, Yoshiteru Ida
  • *School of Pharmaceutical Sciences, Showa University, 1-5-8 Hatanodai, Shinagawa-ku, Tokyo 142-8555, Japan; Fax +81-3-37 84-81 91; E-mail: ida@pharm.showa-u.ac.jp
Further Information

Publication History

Publication Date:
31 December 2000 (online)

A new facile synthesis of 3,4-dihydroxyprolines was attained by taking advantage of the l-threonine aldolase, which catalyzes the aldol condensation reaction of aldehydes with glycine affording β-hydroxy-α-l-amino acids.