Synthesis of All Four Possible Stereoisomers of 5,9-Dimethylpentadecane, the Major Sex Pheromone Component of the Coffee Leaf Miner Moth, Perileucoptera coffeella

@article{Kuwahara2000SynthesisOA,
  title={Synthesis of All Four Possible Stereoisomers of 5,9-Dimethylpentadecane, the Major Sex Pheromone Component of the Coffee Leaf Miner Moth, Perileucoptera coffeella},
  author={S. Kuwahara and T. Liang and W. Leal and J. Ishikawa and O. Kodama},
  journal={Bioscience, Biotechnology, and Biochemistry},
  year={2000},
  volume={64},
  pages={2723 - 2726}
}
  • S. Kuwahara, T. Liang, +2 authors O. Kodama
  • Published 2000
  • Medicine, Biology
  • Bioscience, Biotechnology, and Biochemistry
    • All of the four possible stereoisomers of 5,9-dimethylpentadecane, the major sex pheromone component of the coffee leaf miner moth (Perileucoptera coffeella), were synthesized by using the methyl esters of (S)- and (R)-3-hydroxy-2-methylpropanoic acid as chiral sources for the purpose of determining the stereochemistry of the pheromone. 
    View on Taylor & Francis
    ncbi.nlm.nih.gov
    11 Citations
    Background Citations
    1
    11 Citations
    Citation Type

    Citation Type

    Enantioselective synthesis of three stereoisomers of 5,9-dimethylpentadecane, sex pheromone component of Leucoptera coffeella, from (−)-isopulegol
    • 25
    Synthesis of the (5S,9R)-isomer of 5,9-dimethylpentadecane, the major component of the female sex pheromone of the coffee leaf miner moth, Leucoptera coffeella
    • 10
    Synthesis of All Four Stereoisomers of 6,10,13-Trimethyltetradecan-2-one, a Sex Pheromone Component Produced by Males of the Stink Bug Pallantia macunaima
    • 6
    A new enantioselective synthesis of the four stereoisomers of pallantione, the male-produced sex pheromone of Pallantia macunaima (Heteroptera: Pentatomidae)
    • 1
    Ultrasound assisted synthesis of 5,9-dimethylpentadecane and 5,9-dimethylhexadecane--the sex pheromones of Leucoptera coffeella.
    • 11
    • PDF
    Stereospecific inversion of secondary tosylates to yield chiral methyl-branched building blocks, applied to the asymmetric synthesis of leafminer sex pheromones
    • 11
    Unsymmetrical double Wittig olefination on the syntheses of insect pheromones. Part 1: Synthesis of 5,9-dimethylpentadecane, the sexual pheromone of Leucoptera coffeella
    • 12
    • PDF
    Simple Synthesis of the Major Sex Pheromone Components of Drosophila ananassae and D. pallidosa
    • 5
    Chiral methyl-branched pheromones.
    • 22
    • PDF
    Chemical Analysis of Female Volatiles and Field Response of the Coffee Leafminer Moth (Lepidoptera: Lyonetiidae) to Stereoisomers of Its Major Sex Pheromone Component
    • 2