Successive 1,4- and 1,2-additions of organometallic reagents to a chiral binaphthyl ester: one step synthesis of optically active ketones
- 1 December 1991
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 32 (49) , 7277-7280
- https://doi.org/10.1016/0040-4039(91)80497-t
Abstract
No abstract availableThis publication has 22 references indexed in Scilit:
- Asymmetric conjugate addition of organometallic reagents to chiral α, β-unsaturated estersTetrahedron: Asymmetry, 1991
- Complex-induced proximity effects in enolate formation. Highly diastereoselective α-methylation of binaphthyl esters of arylacetic acids.Tetrahedron Letters, 1990
- Catalytic asymmetric glyoxylate-ene reaction: a practical access to .alpha.-hydroxy esters in high enantiomeric puritiesJournal of the American Chemical Society, 1990
- Centenary Lecture. Chemical multiplication of chirality: science and applicationsChemical Society Reviews, 1989
- Binaphthol as a chiral auxiliary. Asymmetrical alkylation of arylacetic acidTetrahedron Letters, 1989
- Diastereoselective conjugate addition with acetals, oxazolidines and imidazolidines as chiral auxiliariesTetrahedron Letters, 1988
- Allylic stereocenter directed asymmetric conjugate addition of cuprates in the presence of trimethylchlorosilane. enantioselective synthesis of 2-alkyl-4-benzyioxybutanal and 2-alkyl-4-oxopentanalTetrahedron, 1988
- Asymmetric hetero-Diels-Alder reaction catalyzed by a chiral organoaluminum reagentJournal of the American Chemical Society, 1988
- Asymmetric induction in the conjugate addition reactions of chiral organo(hetero)cupratesJournal of the American Chemical Society, 1987
- Enantioselektive Addition von Arylgruppen an aromatische Aldehyde mit Aryltitan‐Binaphthol‐DerivatenEuropean Journal of Inorganic Chemistry, 1985