Influence of cation complexing solvent additives and functional groups in asymmetric alkylations of esters via lithium enolates
- 31 December 1983
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 24 (31) , 3213-3216
- https://doi.org/10.1016/s0040-4039(00)88138-1
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- A total synthesis of enentiomerically pure vitamin e side chain using a chiral propionate synthonTetrahedron Letters, 1983
- High asymmetric induction in diels-alder additions of cyclopentadiene to acrylates derived from isoborneolTetrahedron Letters, 1982
- ChemInform Abstract: SIMPLE, GENERALLY APPLICABLE SYNTHESIS OF N-ACETYLDEHYDROAMINO ACIDSChemischer Informationsdienst, 1982
- An asymmetric synthesis of acyclic and macrocyclic .alpha.-alkyl ketones. The role of (e)- and (z)-lithioenaminesJournal of the American Chemical Society, 1981
- Funktionelle Gruppen in konkaver Lage: Asymmetrische Alkylierung von Estern mit sehr hoher Stereoselektivität und Konfigurationsumkehrung durch SolvensänderungAngewandte Chemie, 1981
- Funktionelle Gruppen in konkaver Lage: Asymmetrische Diels‐Alder‐Synthese mit nahezu vollständiger (Lewis‐Säure‐katalysiert) und hoher (unkatalysiert) StereoselektivitätAngewandte Chemie, 1981
- Synthesis of the stereoisomers of 17,21-dimethylheptatriacontane - sex recognition pheromone of the tsetse flyTetrahedron Letters, 1980
- Cyclization of substituted 5-hexenyl radicals as a model for photocyclization of 1,5-hexadien-3-onesThe Journal of Organic Chemistry, 1980
- Enantioselective alkylation of chiral enolatesTetrahedron Letters, 1980
- The ester enolate Claisen rearrangement. Stereochemical control through stereoselective enolate formationJournal of the American Chemical Society, 1976