Quantitative Trennung der Enantiomerenpaare des Pheromons 2-Ethyl-1,6-dioxaspiro[4,4]nonan durch Komplexierungschromatographie an einem optisch aktiven Metallkomplex
Author:
Publisher
Wiley
Subject
General Medicine
Reference11 articles.
1. 2-Ethyl-1,6-dioxaspiro[4.4]nonane, principal aggregation pheromone of Pityogenes chalcographus (L.)
2. Synthesis of optically active 2-ethyl-1,6-dioxaspiro[4.4]nonane (chalcogran), the principal aggregation pheromone of pityogenes chalcographus (l.)
3. Insect Pheromones; II. Synthesis of Chiral Components of Insect Pheromones
4. Anwendbarkeit von Borkenkäferpheromonen: Konfiguration und Konsequenzen1,2
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1. Determination of Interconversion Barriers by Dynamic Gas Chromatography: Epimerization of Chalcogran;Chemistry;2001-04-01
2. Cyclodextrins as chiral stationary phases in capillary gas chromatography. Part VII: Cyclodextrins with an inverse substitution pattern - synthesis and enantioselectivity;Journal of High Resolution Chromatography;1990-10
3. Structure-activity studies on aggregation pheromone components ofPityogenes chalcographus (Coleoptera: Scolytidae);Journal of Chemical Ecology;1989-02
4. Synthesis and properties of 1,6-dioxaspiro[4.4]nonane and its derivatives (review);Chemistry of Heterocyclic Compounds;1986-09
5. Anwendung von d-Chirasil-Val bei der gas-chromatographischen Analytik von Enantiomeren;Fresenius' Zeitschrift für analytische Chemie;1985-01
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