A rationale of diastereofacial selection in the alkylation of endocyclic enolates with chirality at the β-position
- 31 December 1986
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 27 (28), 3247-3250
- https://doi.org/10.1016/s0040-4039(00)84765-6
Abstract
No abstract availableThis publication has 23 references indexed in Scilit:
- Highly stereoselective intramolecular alkylation of ester enolate: An approach to trans-hydrindane systemTetrahedron Letters, 1986
- Asymmetric additions to chiral naphthalenes. III. The synthesis of (+)-trans-1,2-disubstituted-1,2-dihydronaphthalenesThe Journal of Organic Chemistry, 1986
- Highly diastereoselective tandem alkylation of acyclic α,β-unsaturated esters based on the novel use of dithioacetal unitTetrahedron Letters, 1985
- Control elements in the asymmetric tandem alkylation of α-alkylidene-γ-butyrolactone derivativesTetrahedron Letters, 1985
- l-2-Nitro-1,3-alkanediols by stereoselective addition of nitroethanol to aldehydes. On the asymmetric electrophilic addition to double bondsJournal of the American Chemical Society, 1985
- Stereoelectronic controlling features of allylic asymmetry. Application to ester enolate alkylationsJournal of the American Chemical Society, 1985
- The stereoselective α-alkylation of chiral β-hydroxy esters and some applications thereofTetrahedron, 1984
- Diastereoselective and enantioselective synthesis of 1,2-disubstituted cycloalkanecarboxaldehydesTetrahedron, 1981
- A directing effect of neighboring aromatic groups on the regiochemistry of formation and stereochemistry of alkylation and bromination of ketone lithium enolates. Evidence for lithium-arene coordination and dramatic effect of copper(I) in controlling stereochemistry and limiting polyalkylationJournal of the American Chemical Society, 1979
- Spiroannelation of enol ethers of cyclic 1,3-diketones. Simple stereospecific synthesis of .beta.-vetivoneJournal of the American Chemical Society, 1973