136302-04-0Relevant articles and documents
Enantioselective Synthesis of (S)-(+)-2-Tridecanol Acetate, an Aggregation Pheromone Component of Drosophila mulleri
Enders, Dieter,Plant, Andrew
, p. 1241 - 1243 (2007/10/02)
The enantioselective synthesis of (S)-(+)-2-tridecanol acetate (ee = 93.5percent), an aggregation pheromone of Drosophila mulleri, is described.Key steps are the α-alkylation of the propiophenone SAMP-hydrazone (S)-2 (de 96percent) and the Baeyer-Villiger reaction of the ketone (S)-4.Key Words: (S)-(+)-2-Tridecanol acetate / SAMP-hydrazone / Baeyer-Villiger reaction / Pheromone, aggregation / Drosophila mulleri