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Synthesis of the optically active forms of 4,10-dihydroxy-1,7-dioxaspiro[5.5]undecane and their conversion to the enantiomers of 1,7-dioxaspiro[5.5]undecane,the olive fly pheromone
Authors:Kenji Mori  Tamon Uematsu  Kazunori Yanagi  Masao Minobe
Affiliation:1. Department of Agricultural Chemistry, The University of Tokyo, Yayoi 1-1-1, Bunkyo-ku Tokyo 113 Japan;2. Takatsuki Research Laboratory, Sumitomo Chemical Co, Ltd., Tsukahara 2-10-1, Takatsuki-shi Osaka 569 Japan
Abstract:Both the enantiomers of l,7-dioxaspiro[5.5]undecane, the major component of the pheromone of the olive fly (Dacus oleae), were synthesized from (S)-malic acid.
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