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Z Naturforsch C J Biosci ; 58(1-2): 109-12, 2003.
Article in English | MEDLINE | ID: mdl-12622236

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.


Subject(s)
Fatty Alcohols/chemistry , Phaeophyceae/chemistry , Sex Attractants/chemistry , Fatty Alcohols/chemical synthesis , Fatty Alcohols/isolation & purification , Indicators and Reagents , Japan , Sex Attractants/chemical synthesis , Sex Attractants/isolation & purification , Stereoisomerism
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