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Pheromone Synthesis, CLXIV. Synthesis of (2 S , 6 Z )‐6,8‐Nonadien‐2‐ol, a Pheromone Component of the Leafminer Nepticula malella , and Its Antipode
Author(s) -
Mori Kenji,
Ogita Haruhisa
Publication year - 1994
Publication title -
liebigs annalen der chemie
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.825
H-Index - 155
eISSN - 1099-0690
pISSN - 0170-2041
DOI - 10.1002/jlac.199419941104
Subject(s) - chemistry , pheromone , enantiomer , lipase , hydrolysis , stereochemistry , component (thermodynamics) , enantioselective synthesis , catalysis , sex pheromone , organic chemistry , enzyme , botany , physics , biology , thermodynamics
Both the enantiomers of (Z)‐6,8‐nonadien‐2‐ol were synthesized via lipase‐catalyzed asymmetric hydrolysis of the acetate of its racemate, which was prepared from ethyl levulinate.