Stereoselective synthesis of the both enantiomers of disparlure, the pheromone of the gypsy moth
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference17 articles.
1. Potent Sex Attractant of the Gypsy Moth: Its Isolation, Identification, and Synthesis
2. Pheromone III Eine stereoselektive synthese von 7,8-z-epoxy-2-methyloctadecan, dem sexuallockstoff des schwammspinners (lymantria dispar, porthetria dispar, lepidoptera)
3. Synthesis of alkenes from carbonyl compounds and carbanions alpha to silicon. III. Full report and a synthesis of the sex pheromone of gypsy moth
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1. Formal Synthesis of Sex Pheromone of Gypsy Moth (+)-Disparlure from L-(+)-Tartaric Acid;J KOREAN CHEM SOC;2024
2. Overview of Kenji Mori’s pheromone synthesis series;Journal of Pesticide Science;2023-02-20
3. Organocatalyzed epoxidation in the total synthesis of (−)-trans-, (+)-trans- and (+)-cis-disparlures;Organic & Biomolecular Chemistry;2023
4. Synthesis of disparlure and monachalure enantiomers from 2,3-butanediacetals;Beilstein Journal of Organic Chemistry;2020-04-03
5. Synthesis of Isotopically Labelled Disparlure Enantiomers and Application to the Study of Enantiomer Discrimination in Gypsy Moth Pheromone-Binding Proteins;European Journal of Organic Chemistry;2019-10-18
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