Pheromone Syntheses, LXXVII. New Synthesis of the Enantiomers of 14-Methyl-1-octadecene, the Pheromone ofLyonetia clerkella L.
Author:
Publisher
Wiley
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Organic Chemistry,Physical and Theoretical Chemistry
Reference10 articles.
1. Sex Pheromone of the Peach Leafminer Moth, Lyonetia clerkella LINNE : Isolation and Identification
2. Improved synthesis of 14-methyl-1-octadecene, the sex pheromone of the peach leafminer moth.
3. Stereocontrolled synthesis of all of the possible stereoisomers of 3,11-dimethylnonacosan-2-one and 29-hydroxy-3,11-dimethylnonacosan-2-one
4. Synthesis and biological activity of both (E)- and (Z)-isomers of optically pure (S)-14-methyl-8-hexadecenal (trogodermal), the antipodes of the pheromone of the khapra beetle
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1. Neutral iridium catalysts with chiral phosphine-carboxy ligands for asymmetric hydrogenation of unsaturated carboxylic acids;Chemical Science;2017
2. A Facile Asymmetric Synthesis of (S)-14-Methyl-1-Octadecene, the Sex Pheromone of the Peach Leafminer Moth;Molecules;2013-05-07
3. Improved Synthesis of Three Methyl-Branched Pheromone Components Produced by the Female Lichen Moth;Bioscience, Biotechnology, and Biochemistry;2010-01-23
4. The Synthesis of Insect Pheromones, 1979-1989;Total Synthesis of Natural Products;2007-02-20
5. Insect Pheromones Synthesized by Oxidative Transformations of Natural Monoterpenoids;Chemistry of Natural Compounds;2005-11
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