A new synthesis of the enantiomers of ipsdienol, the pheromone of the IPS bark beetles
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference16 articles.
1. Immunologic Maturation in utero : Kinetics of the Primary Antibody Response in the Fetal Lamb
2. Absolute configuration of (+)-ipsdienol, the pheromone of lanier, as determined by the synthesis of its (R)-(-)-isomer
3. Pheromonal chirality and integrity of aggregation response in southern species of the bark beetle Ips sp.
4. Inhibition of the attractive pheromone response in Ips paraconfusus by (R)-(?)-ipsdienol
5. Pheromonal attraction and allomonal interruption ofIps pini in California by the two enantiomers of ipsdienol
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1. The Synthesis of Ipsenol and Ipsdienol: A Review (1968–2020);The Chemical Record;2021-02-04
2. Enantioselective Isoprenylboration Reaction of Aldehydes Catalyzed by a Chiral Phosphoric Acid;Advanced Synthesis & Catalysis;2019-05-02
3. Enantioselective iridium-catalyzed carbonyl isoprenylation via alcohol-mediated hydrogen transfer;Chemical Communications;2019
4. Isopropylidenetriphenylphosphorane;Encyclopedia of Reagents for Organic Synthesis;2013-09-16
5. Stereoselective synthesis of (R)- and (S)-Ipsdienols, pheromone components of bark beetles of the Ips family;Russian Journal of Organic Chemistry;2012-09
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