Pheromone synthesis. Part 76. Synthesis of the enantiomers of 14-methyl-1-octadecene, the sex pheromone of the peach leafminer moth.
Author:
Publisher
Oxford University Press (OUP)
Subject
General Agricultural and Biological Sciences,General Biochemistry, Genetics and Molecular Biology
Cited by 7 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Improved Synthesis of Three Methyl-Branched Pheromone Components Produced by the Female Lichen Moth;Bioscience, Biotechnology, and Biochemistry;2010-01-23
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3. Relative and absolute stereochemistry of the fumonisin B2 backbone;Tetrahedron Letters;1994-09
4. Lipase-catalyzed resolution of racemic 2-alkyl substituted 1-alkanols;Tetrahedron: Asymmetry;1993-05
5. Pheromone synthesis, CXXIX. Synthesis of the (5S,9S)-isomers of 5,9-Dimethylheptadecane and 5,9-dimethyloctadecane, the major and the minor components of the sex pheromone ofLeucoptera malifoliella costa;Liebigs Annalen der Chemie;1991-05-16
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