Stereoselective synthesis of β-amino alcohols: diastereoselective reduction of chiral α′-amino enones derived from amino acids
- 25 September 1997
- journal article
- research article
- Published by Elsevier in Tetrahedron: Asymmetry
- Vol. 8 (18) , 3027-3030
- https://doi.org/10.1016/s0957-4166(97)00374-1
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- Preparation of Aminoalkyl Chlorohydrin Hydrochlorides: Key Building Blocks for Hydroxyethylamine-Based HIV Protease InhibitorsThe Journal of Organic Chemistry, 1996
- Highly syn-Selective Additions of Allylic Stannanes to Protected .alpha.-Amino AldehydesThe Journal of Organic Chemistry, 1994
- CrCl2 mediated allylation of N-protected α-amino aldehydes. A versatile synthesis of polypeptides containing an hydroxyethylene isostereTetrahedron Letters, 1994
- A simple method for chelation controlled additions to α-amino aldehydesTetrahedron Letters, 1994
- Lewis acid-mediated reaction with silyl ketene acetals and allylstannane of the aluminum acetals generated by DIBALH reduction of α-amino acid estersTetrahedron Letters, 1993
- Structural, mechanistic, and theoretical aspects of chelation-controlled carbonyl addition reactionsAccounts of Chemical Research, 1993
- Discovery of a novel class of potent HIV-1 protease inhibitors containing the (R)-(hydroxyethyl)urea isostereJournal of Medicinal Chemistry, 1993
- New Approaches to the Use of Amino Acids as Chiral Building Blocks in Organic Synthesis [New Synthetic Methods (85)]Angewandte Chemie International Edition in English, 1991
- Optically active N-protected .alpha.-amino aldehydes in organic synthesisChemical Reviews, 1989
- Stereoselective Synthesis of β‐Amino Alcohols from Optically Active α‐Amino AcidsAngewandte Chemie International Edition in English, 1987