Direct amination of β-oxo esters
- 5 February 2001
- journal article
- research article
- Published by Elsevier in Tetrahedron Letters
- Vol. 42 (6), 1171-1173
- https://doi.org/10.1016/s0040-4039(00)02200-0
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Conjugate addition to diethyl azodicarboxylate under organic-perfluorinated biphasic homogeneous catalysis by nickel(II) speciesTetrahedron Letters, 2000
- Stereoselective reductive amination of β-keto esters derived from dipeptides. Stereochemical and mechanistic studies on the formation of 5-carboxymethyl-2-oxopiperazine derivativesTetrahedron, 1999
- Synthesis of Hydroxamic Esters via Alkoxyaminocarbonylation of β-Dicarbonyl CompoundsThe Journal of Organic Chemistry, 1999
- Easy access to α-amino β-oxo esters from β-enamino estersTetrahedron Letters, 1999
- Enantioselective conjugate additions of silylketene acetals to 2-carboxycyclopentenones promoted by chiral Ti complexesTetrahedron, 1997
- Asymmetric synthesis of α-amino acid derivatives via an electrophilic amination of chiral amide cuprates with Li t-butyl-N-tosyloxycarbamateTetrahedron Letters, 1997
- Diastereoselective alkylation of chiral derivatives of acetoacetic acidTetrahedron, 1995
- Asymmetric Synthesis of AntiN-Boc-α-Hydrazino-β-Hydroxyesters from β-Ketoesters by Sequential Catalytic Hydrogenation and Electrophilic AminationSynlett, 1993
- Enantiospecific and diastereoselective synthesis of anti α-hydrazino- and α-amino-β-hydroxyacids through “electrophilic amination” of β-hydroxyestersTetrahedron, 1987