Enahtioselective synthesis of sitophilate, the granary weevil aggregation pheromone
- 1 January 1989
- journal article
- research article
- Published by Elsevier in Tetrahedron
- Vol. 45 (3) , 623-628
- https://doi.org/10.1016/0040-4020(89)80090-0
Abstract
No abstract availableThis publication has 33 references indexed in Scilit:
- Regioselective opening of 2,3-epoxy alcohols with organocuprates. Enhanced C-2 selectivity through solvent effects.Tetrahedron Letters, 1987
- The chemical identification of the granary weevil aggregation pheromoneTetrahedron Letters, 1987
- Catalytic asymmetric epoxidation and kinetic resolution: modified procedures including in situ derivatizationJournal of the American Chemical Society, 1987
- Stereoselective Aldol Reactions with α‐Unsubstituted Chiral EnolatesAngewandte Chemie International Edition in English, 1987
- Double Asymmetric Synthesis and a New Strategy for Stereochemical Control in Organic SynthesisAngewandte Chemie International Edition in English, 1985
- Regioselective openings of 2,3-epoxy acids with organocupratesTetrahedron Letters, 1985
- Stereoselective Aldol CondensationsTopics in Stereochemistry, 1982
- The first practical method for asymmetric epoxidationJournal of the American Chemical Society, 1980
- 13C NMR of some insect attractants and related compoundsTetrahedron, 1978
- .alpha.-Methoxy-.alpha.-trifluoromethylphenylacetic acid, a versatile reagent for the determination of enantiomeric composition of alcohols and aminesThe Journal of Organic Chemistry, 1969