Asymmetric grignard addition to aldéhydes. An example of inverse temperature dependence of enantiomeric excess.
- 30 April 1994
- journal article
- research article
- Published by Elsevier in Tetrahedron: Asymmetry
- Vol. 5 (4) , 569-572
- https://doi.org/10.1016/0957-4166(94)80020-0
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- C2 symmetry and asymmetric inductionChemical Reviews, 1989
- Enantioselective alkylation of carbonyl compounds. From stoichiometric to catalytic asymmetric inductionPublished by Walter de Gruyter GmbH ,1988
- Novel 3,4-Diarylpyrrolidine-Based Chiral Ligands for the Asymmetric Reaction of Arylmagnesium Bromides with AldehydesChemistry Letters, 1987
- Stereoselective addition reaction of diethylzinc to aldehydes, catalyzed by cinchona alkaloidsThe Journal of Organic Chemistry, 1987
- Enantioselektive Addition von Arylgruppen an aromatische Aldehyde mit Aryltitan‐Binaphthol‐DerivatenEuropean Journal of Inorganic Chemistry, 1985
- Chiral catalysis of additions of alkyllithiums to aldehydesJournal of the American Chemical Society, 1981
- Enantioface-differentiating (asymmetric) addition of alkyllithium and dialkylmagnesium to aldehydes by using (2S,2'S)-2-hydroxymethyl-1-[(1-alkylpyrrolidin-2-yl)methyl]pyrrolidines as chiral ligandsJournal of the American Chemical Society, 1979
- Asymmetric synthesis. Part IV. The stereoselectivity of grignard-carbonyl reactions in solvents that contain carbohydratesTetrahedron Letters, 1969
- Asymmetric carbinol synthesis by means of (−)-sparteine-modified organometallic reagentsTetrahedron Letters, 1968
- Electronic Control of Steric Hindrance in Hindered Phenols1The Journal of Organic Chemistry, 1957