Pheromones of insects and their analogs. LII. Sythesis of dodec-9-en-1-yl and tetradec-11-en-1-yl acetates from the products of the partial ozonolysis of cycloocta-1z,5z-diene and cyclodeca-1e,5z-diene
A new approach to the synthesis of octane-1,8-and decane-1,10-diols based on the partial ozonolysis of cyclic oligomers has been developed.
Odinokov,Botsman,Gladysheva
p. 381 - 383
(2007/10/03)
Synthesis of (S,E)-1-Methyl-9-dodecenyl Acetate, the Sex Pheromone of the Hessian Fly, Mayetiola destructor, by Lipase-catalyzed Enantioselective Hydrolysis
(S,E)-1-Methyl-9-dodecenyl acetate , the sex pheromone of the hessian fly, Mayetiola destructor, was synthesized in a highly enantiomerically pure form by Pseudomonas cepacia lipase-catalyzed hydrolysis.