Bioscience, Biotechnology and Biochemistry p. 2723 - 2726 (2000)
Update date:2022-07-29
Topics:
Kuwahara, Shigefumi
Liang, Ting
Leal, Walter Soares
Ishikawa, Jiro
Kodama, Osamu
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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Doi:10.1002/cmdc.201600248
(2016)Doi:10.1021/jo00837a613
(1970)Doi:10.1055/s-2000-6224
(2000)Doi:10.1007/BF00957365
()Doi:10.1093/bioinformatics/17.1.83
(1891)Doi:10.1562/2005-06-20-RA-581
(2006)
