Regioselective preparation of α-nitro cyclohexyl triisopropylsilyl enol ethers
- 1 November 1994
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 35 (45) , 8345-8348
- https://doi.org/10.1016/s0040-4039(00)74403-0
Abstract
No abstract availableThis publication has 38 references indexed in Scilit:
- Asymmetric synthesis of α-amino acids and α-N-hydroxyamino acids via electrophilic amination of bornanesultam-derived enolates with 1-chloro-1-nitrosocyclohexane.Tetrahedron Letters, 1990
- Stereoselective preparation of synthetic equivalents of 2-deoxy-2-amino- and 3-deoxy-3-aminotetroses from malic acid. Application to the synthesis of C18-D-ribo-phytosphingosineTetrahedron Letters, 1989
- The asymmetric synthesis of α-amino and α-hydrazino acid derivatives via the stereoselective amination of chiral enolates with azodicarboxylate estersTetrahedron, 1988
- Enantioselective systheses of α-amino acids from 10-sulfonamido-isobornyl esters and di-t-butyl azodicarboxylateTetrahedron, 1988
- Enantiospecific and diastereoselective synthesis of anti α-hydrazino- and α-amino-β-hydroxyacids through “electrophilic amination” of β-hydroxyestersTetrahedron, 1987
- Electrophilic azide transfer to chiral enolates. A general approach to the asymmetric synthesis of .alpha.-amino acidsJournal of the American Chemical Society, 1987
- Asymmetric halogenation of chiral imide enolates. A general approach to the synthesis of enantiomerically pure α-amino acids.Tetrahedron Letters, 1987
- Amination of chiral enolates by dialkyl azodiformates. Synthesis of .alpha.-hydrazino acids and .alpha.-amino acidsJournal of the American Chemical Society, 1986
- Stereoselective amination of chiral enolates. A new approach to the asymmetric synthesis of .alpha.-hydrazino and .alpha.-amino acid derivativesJournal of the American Chemical Society, 1986
- Asymmetric electrophilic amination: synthesis of .alpha.-amino and .alpha.-hydrazino acids with high optical purityJournal of the American Chemical Society, 1986