Premium
Pheromone Synthesis, CXIII. Synthesis of the Enantiomers of (3 Z ,6 Z )‐ cis ‐9,10‐Epoxy‐1,3,6‐henicosatriene and (3 Z ,6 Z )‐ cis ‐9,10‐Epoxy‐1,3,6‐icosatriene, the New Pheromone Components of Hyphantria cunea
Author(s) -
Mori Kenji,
Takeuchi Tadashi
Publication year - 1989
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.198919890180
Subject(s) - chemistry , enantiomer , stereochemistry , sharpless epoxidation , enantioselective synthesis , pheromone , epoxy , sex pheromone , organic chemistry , catalysis , botany , biology
The synthesis of (9 S ,10 R )‐epoxytrienes 1 and 2 as well as their antipodes was achieved employing the asymmetric Sharpless epoxidation as the key step.