Title: | "Biomimetic conversion of (3S)-(-)-neodictyoprolenol to optically pure (1S,2R)-(-)-dictyopterene B, marine algal sex pheromone" |
Author(s): | Kajiwara T; Yamamoto Y; Akakabe Y; Matsui K; Shimizu H; Kawai T; |
Address: | "Department of Biological Chemistry, Faculty of Agriculture, Yamaguchi University, Yamaguchi 753-8515, Japan. kajiwara@agr.yamaguchi-u.ac.jp" |
ISSN/ISBN: | 0939-5075 (Print) 0341-0382 (Linking) |
Abstract: | "Both enantiomers of (3S)-(-)- and (3R)-(+)-Neodictyoprolenol [(3S,5Z,8Z)-(-)-1,5,8-undecatrien-3-ol] were successfully converted to the algal sex pheromone, (1S,2R)-(-)-dictyopterene B and (1R,2S)-(+)-dictyopterene B in high enantiomeric purities (e. e. > 99%), respectively, by the biomimetic reaction involving phosphorylation and elimination under a mild condition" |
Keywords: | Fatty Alcohols/chemical synthesis/*chemistry/isolation & purification Indicators and Reagents Japan Phaeophyta/*chemistry Sex Attractants/chemical synthesis/*chemistry/isolation & purification Stereoisomerism; |
Notes: | "MedlineKajiwara, Tadahiko Yamamoto, Yuuko Akakabe, Yoshihiko Matsui, Kenji Shimizu, Hiroshi Kawai, Tesuo eng Research Support, Non-U.S. Gov't Germany 2003/03/08 Z Naturforsch C J Biosci. 2003 Jan-Feb; 58(1-2):109-12. doi: 10.1515/znc-2003-1-219" |