Asymmetric Synthesis of 2-Amino Alcohol Derivatives from (S)-α-Amino Aldehydes via Chiral Acetal Templates
- 5 August 1987
- journal article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 16 (8), 1531-1534
- https://doi.org/10.1246/cl.1987.1531
Abstract
No abstract availableThis publication has 13 references indexed in Scilit:
- Inhibition of cathepsin D by substrate analogs containing statine and by analogs of pepstatinJournal of Medicinal Chemistry, 1986
- Asymmetric simmons-smith reactions using homochiral protecting groupsTetrahedron, 1986
- Chiral synthesis of statineTetrahedron Letters, 1985
- Pepstatin-derived inhibitors of aspartic proteinases. A close look at an apparent transition-state analog inhibitorJournal of Medicinal Chemistry, 1985
- Asymmetric synthesis via chiral acetal templates. 7. Further studies on the cyanation reaction. The use of acetals derived from diols with one chiral centerTetrahedron Letters, 1984
- Nucleophilic cleavages of acetals using organotitanium reagents. A new synthesis of chiral alcoholsTetrahedron Letters, 1984
- Synthesis of hydroxyethylene and ketomethylene dipeptide isosteresTetrahedron Letters, 1983
- Tetralithiotetrahedrane: is it a minimum?Journal of the American Chemical Society, 1983
- Synthesis of (3S,4S)-4-amino-3-hydroxy-6-methylheptanoic acid derivatives. Analysis of diastereomeric purityThe Journal of Organic Chemistry, 1978
- Oxidation of alcohols by “activated” dimethyl sulfoxide. a preparative, steric and mechanistic studyTetrahedron, 1978