Literature DB >> 11210147

Synthesis of all four possible stereoisomers of 5,9-dimethylpentadecane, the major sex pheromone component of the coffee leaf miner moth, Perileucoptera coffeella.

S Kuwahara1, T Liang, W S Leal, J Ishikawa, O Kodama.   

Abstract

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.

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Year:  2000        PMID: 11210147     DOI: 10.1271/bbb.64.2723

Source DB:  PubMed          Journal:  Biosci Biotechnol Biochem        ISSN: 0916-8451            Impact factor:   2.043


  2 in total

1.  Ultrasound assisted synthesis of 5,9-dimethylpentadecane and 5,9-dimethylhexadecane--the sex pheromones of Leucoptera coffeella.

Authors:  Nhuan Ngoc Doan; Thach Ngoc Le; Hao Cong Nguyen; Poul Erik Hansen; Fritz Duus
Journal:  Molecules       Date:  2007-08-28       Impact factor: 4.411

2.  Total Synthesis of (-)-Bastimolide A: A Showcase for Type I Anion Relay Chemistry.

Authors:  Joshua B Cox; Alex A Kellum; Yiwen Zhang; Bo Li; Amos B Smith
Journal:  Angew Chem Int Ed Engl       Date:  2022-05-24       Impact factor: 16.823

  2 in total

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