Preparation of highly enantiopure β-amino esters by Candida antarctica lipase A
- 1 February 2001
- journal article
- Published by Elsevier in Tetrahedron: Asymmetry
- Vol. 12 (1) , 105-110
- https://doi.org/10.1016/s0957-4166(01)00002-7
Abstract
No abstract availableKeywords
This publication has 20 references indexed in Scilit:
- Application of a new chiral stationary phase containing the glycopeptide antibiotic A-40,926 in the direct chromatographic resolution of β-amino acidsTetrahedron: Asymmetry, 2000
- De Novo Design of Antibacterial β-PeptidesJournal of the American Chemical Society, 1999
- Enzymatic methods for the preparation of enantiopure malic and aspartic acid derivatives in organic solventsTetrahedron: Asymmetry, 1999
- Sequential resolution of ethyl 3-aminobutyrate with carboxylic acid esters by Candida antarctica lipase BTetrahedron: Asymmetry, 1999
- Biocatalysis for the preparation of optically active β-lactam precursors of amino acidsTetrahedron: Asymmetry, 1996
- Enantioselective Synthesis of β‐Amino Acids: TMS‐SAMP as a Chiral Ammonia Equivalent for the Aza Analogous Michael Addition to α,β‐Unsaturated EstersAngewandte Chemie International Edition in English, 1995
- Enzymatic acylation in the resolution of methyl threo-2-hydroxy-3-(4-methoxyphenyl)-3-(2-X-phenylthio)propionates in organic solventsJournal of the Chemical Society, Perkin Transactions 1, 1993
- Quantitative analyses of biochemical kinetic resolutions of enantiomersJournal of the American Chemical Society, 1982
- Studies on Potential Antitumor Agents (III). Synthesis of 4-ArylcyclophosphamidesHETEROCYCLES, 1978
- Herstellung und Umsetzungen von ?-LactamenHelvetica Chimica Acta, 1968