Synthesis of all the stereoisomers of 13,17-dimethyl-1-tritriacontene and 13,17-dimethyl-1-pentatriacontene, the contact sex pheromone components of the female tsetse fly, Glossina austeni
T. Kimura et al., Synthesis of all the stereoisomers of 13,17-dimethyl-1-tritriacontene and 13,17-dimethyl-1-pentatriacontene, the contact sex pheromone components of the female tsetse fly, Glossina austeni, EUR J ORG C, (17), 2001, pp. 3385-3390
All of the stereoisomers of 13,17-dimethyl-1-tritriacontene (1) and 13,17-d
imethyl-1-pentatriacontene (2), the contact Sex pheromone components of the
female tsetse fly (Glossina austeni), were synthesized starting from the e
nantiomers of the protected syn- and anti-2,6-dimethylheptane-1,7-diol (3),
which were prepared from the enantiomers of methyl 3-hydroxy-2-methylpropa
noate (4) and methyl phenyl sulfone (5).