Stereoselective synthesis of the both enantiomers of disparlure, the pheromone of the gypsy moth
- 1 January 1979
- journal article
- research article
- Published by Elsevier in Tetrahedron
- Vol. 35 (7) , 833-837
- https://doi.org/10.1016/0040-4020(79)80102-7
Abstract
No abstract availableThis publication has 13 references indexed in Scilit:
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- A stereospecific synthesis of (+)-disparlure, sex attractant of the gypsy mothTetrahedron Letters, 1977
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- The synthesis of alkenes from carbonyl compounds and carbanions α to silicon V. Stereoselective synthesis ofTetrahedron Letters, 1976
- Stereoselective synthesis of optically active disparlure, the pheromone of the gypsy moth (Tetrahedron Letters, 1976
- Pheromone III Eine stereoselektive synthese von 7,8-z-epoxy-2-methyloctadecan, dem sexuallockstoff des schwammspinners (lymantria dispar, porthetria dispar, lepidoptera)Tetrahedron Letters, 1974
- Synthesis and activity of optically active disparlureJournal of the American Chemical Society, 1974
- Synthesis of alkenes from carbonyl compounds and carbanions alpha to silicon. III. Full report and a synthesis of the sex pheromone of gypsy mothThe Journal of Organic Chemistry, 1974
- Nuclear magnetic resonance enantiomer regents. Configurational correlations via nuclear magnetic resonance chemical shifts of diastereomeric mandelate, O-methylmandelate, and .alpha.-methoxy-.alpha.-trifluoromethylphenylacetate (MTPA) estersJournal of the American Chemical Society, 1973
- Potent Sex Attractant of the Gypsy Moth: Its Isolation, Identification, and SynthesisScience, 1970