Insect pheromones and their analogs. LX. Stereocontrolled synthesis of sexpheromones of Drosophila mulleri and Mayetiola destructor

Citation
Ry. Kharisov et al., Insect pheromones and their analogs. LX. Stereocontrolled synthesis of sexpheromones of Drosophila mulleri and Mayetiola destructor, CHEM NAT CO, 36(2), 2000, pp. 210-212
Citations number
12
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
CHEMISTRY OF NATURAL COMPOUNDS
ISSN journal
00093130 → ACNP
Volume
36
Issue
2
Year of publication
2000
Pages
210 - 212
Database
ISI
SICI code
0009-3130(200003/04)36:2<210:IPATAL>2.0.ZU;2-3
Abstract
Syntheses are developed for 2S-tridecyl- and 2S-tridec-10E-enylacetates, se x pheromones of the fruit fly Drosophila mulleri and the Hessian fly Mayeti ola destructor, respectively, that are based on ethyl-3S-hydroxybutanoate, a product from enzymatic reduction of ethyl acetoacetate by the soil yeast strain "80-1."