Synthesis of all the stereoisomers of 6-methyl-2-octadecanone, 6,14-dimethyl-2-octadecanone, and 14-methyl-2-octadecanone, the components of the female-produced sex pheromone of a moth, Lyclene dharma dharma
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference24 articles.
1. Syntheses of 2-Isopropyl-4,5-dihydrothiazole and 6-Hydroxy-6-methyl-3-heptanone, Pheromone Components of the Male Mouse,Mus musculus
2. A Novel Lepidopteran Sex Pheromone Produced by Females of a Lithosiinae Species,Lyclene dharma dharma, in the Family of Arctiidae
3. Significance of chirality in pheromone science
4. Synthesis of all the six components of the female-produced contact sex pheromone of the German cockroach, Blattella germanica (L.)
5. New Approaches to Olefin Cross-Metathesis
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1. Enantioselective Synthesis of the Active Sex Pheromone Components of the Female Lichen Moth, Lyclene dharma dharma, and Their Enantiomers;Molecules;2024-06-19
2. Copper‐Catalyzed Coupling Reaction of Secondary Alkyl 2‐Pyridinesulfonates with Alkyl Lithium‐Based Reagents;European Journal of Organic Chemistry;2023-06-26
3. Alkene Cross‐Metathesis Reactions;Organic Reactions;2021-06-15
4. Enantioselective Synthesis and Activity of All Diastereoisomers of (E)-Phytal, a Pheromone Component of the Moroccan Locust, Dociostaurus maroccanus;Journal of Agricultural and Food Chemistry;2018-12-17
5. Synthesis of Semiochemicals via Olefin Metathesis;ACS Sustainable Chemistry & Engineering;2018-11-29
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