Pheromone synthesis. Part 258. Synthesis of the enantiomers of the beetle pheromones ethyl 4-methylheptanoate, 4-methyloctanoic acid and 4-methyl-1-nonanol, and HPLC analysis of their derivatives to determine their enantiomeric purities
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis
Reference19 articles.
1. Pheromone synthesis. Part 257: Synthesis of methyl (2E,4Z,7Z)-2,4,7-decatrienoate and methyl (E)-2,4,5-tetradecatrienoate, the pheromone components of the male dried bean beetle, Acanthoscelides obtectus (Say)
2. Chiral methyl-branched pheromones
3. Significance of chirality in pheromone science
4. Stereochemical studies on pheromonal communications
5. Pheromone synthesis. Part 245: Synthesis and chromatographic analysis of the four stereoisomers of 4,8-dimethyldecanal, the male aggregation pheromone of the red flour beetle, Tribolium castaneum
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3. Defining Pathways of Anaerobic Alkane Oxidation: Synthesis of Enantiomers of 4‐Methylalkanoic Acids and (2‐Methylalkyl)malonic Acids;ChemistrySelect;2021-04-28
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