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

Hiromasa Kiyota

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

Faculty of Agriculture

Research output: Contribution to journal › Article

Original language	English
Pages (from-to)	865-870
Number of pages	6
Journal	Liebigs Annalender Chemie
Volume	1993
Publication status	Published - 1993

Cite this

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. / Kiyota, Hiromasa.
In: Liebigs Annalender Chemie, Vol. 1993, 1993, p. 865-870.

Research output: Contribution to journal › Article

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title = "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",

author = "Hiromasa Kiyota",

year = "1993",

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volume = "1993",

pages = "865--870",

journal = "Liebigs Annalender Chemie",

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AU - Kiyota, Hiromasa

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JF - Liebigs Annalender Chemie

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