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- W2031119178 abstract "The relative configuration of the naturally occurring 3-methyl-4-octanol (1), the male-produced aggregation pheromone of Rhynchophorus phoenicis, was determined as syn by a GC comparison of the synthetic (±)-syn- and (±)-anti-1 with the natural product. Enantioselective synthesis of both (3R,4R)-and (3S,4S)-1 was achieved by starting from the optically active epoxide 9, and the natural product was shown to be (3S,4S)-1 by a GC comparison on a chiral stationary phase." @default.
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- W2031119178 date "1993-08-12" @default.
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- W2031119178 title "Pheromone Synthesis, CLIV. Synthesis of the Stereoisomers of 3-Methyl-4-octanol to Determine the Absolute Configuration of the Naturally Occurring (3S,4S)-Isomer Isolated as the Male-produced Aggregation Pheromone of the African Palm Weevil,Rhynchophorus phoenicis" @default.
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- W2031119178 doi "https://doi.org/10.1002/jlac.1993199301137" @default.
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