Synlett 1995; 1995(11): 1097-1109
DOI: 10.1055/s-1995-5191
account
© 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.

Biochemical Methods in Enantioselective Synthesis of Bioactive Natural Products

Kenji Mori*
  • *Department of Chemistry, Faculty of Science, Science University of Tokyo, Kagurazaka 1-3, Shinjuku-ku, Tokyo 162, Japan, Fax 81-3-3235-2214
Further Information

Publication History

Publication Date:
31 December 2000 (online)

Hydrolytic enzymes and microorganisms were employed in enantioselective syntheses of bioregulators such as hormones and pheromones. Esterases and lipases were useful in achieving optical resolution, conversion of meso-compounds to optically active compounds, and macrolactonization. Yeasts provided a variety of optically active hydroxy ketones and esters, which served as versatile non-racemic chiral building blocks.

    >