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

Research output: Contribution to journalArticle

17 Citations (Scopus)
Original languageEnglish
Pages (from-to)865-870
Number of pages6
JournalLiebigs Annalender Chemie
Volume1993
Publication statusPublished - 1993

Cite this

@article{0953d9ca249d4cadbb90d5973d470a63,
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",
language = "English",
volume = "1993",
pages = "865--870",
journal = "Liebigs Annalender Chemie",

}

TY - JOUR

T1 - 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

AU - Kiyota, Hiromasa

PY - 1993

Y1 - 1993

M3 - Article

VL - 1993

SP - 865

EP - 870

JO - Liebigs Annalender Chemie

JF - Liebigs Annalender Chemie

ER -