Absolute configuration of (+)-ipsdienol, the pheromone of lanier, as determined by the synthesis of its (R)-(-)-isomer
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference18 articles.
1. Immunologic Maturation in utero : Kinetics of the Primary Antibody Response in the Fetal Lamb
2. Methodology for Isolation and Identification of Insect Pheromones with Reference to Studies on California Five-Spined Ips1
3. Synthesis of the principal components of the sex attractant from male Ips confusus frass: 2-methyl-6-methylene-7-octen-4-ol, 2-methyl-6-methylene-2,7-octadien-4-ol, and (+)-cis-verbenol
4. Improved synthesis of 2-methyl-6-methylene-2,7-octadien-4-ol, a pheromone of Ips paraconfusus, and an alternative synthesis of the intermediate, 2-bromomethyl-1,3-butadiene
5. Pheromone synthesis. III. A new synthesis of 2-methyl-6-methyleneocta-2,7-dien-4-ol, A component of the pheromone of california five-spined Ips.
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1. The Synthesis of Ipsenol and Ipsdienol: A Review (1968–2020);The Chemical Record;2021-02-04
2. Stereoselective synthesis of (R)- and (S)-Ipsdienols, pheromone components of bark beetles of the Ips family;Russian Journal of Organic Chemistry;2012-09
3. Synthesis of Pheromones;Chemical Synthesis of Hormones, Pheromones and Other Bioregulators;2010-08-13
4. Bark beetle pheromones: evidence for physiological synthesis mechanisms and their ecological implications;Zeitschrift für Angewandte Entomologie;2009-08-26
5. Oxygenated terpenes in pheromone systems of bark beetles1;Zeitschrift für Angewandte Entomologie;2009-08-26
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