Enzymatic resolution of (±)-trans-2-aminocyclohexanol and (±)-trans-2-aminocyclopentanol
- 25 September 1997
- journal article
- Published by Elsevier in Tetrahedron: Asymmetry
- Vol. 8 (18), 3153-3159
- https://doi.org/10.1016/s0957-4166(97)00368-6
Abstract
No abstract availableKeywords
Funding Information
- Comisión Interministerial de Ciencia y Tecnología (BIO-95-0687)
- Novo Nordisk
This publication has 26 references indexed in Scilit:
- Practical Synthesis of Enantiopure Cyclic 1,2-Amino Alcohols via Catalytic Asymmetric Ring Opening of Meso EpoxidesThe Journal of Organic Chemistry, 1997
- Combinatorial Approach to the Discovery of Novel Coordination ComplexesJournal of the American Chemical Society, 1996
- Sequential biocatalytic resolution of (±)-trans-cyclohexane-1,2-diamine. Chemoenzymatic synthesis of an optically active polyamineChemical Communications, 1996
- Enzymatic Preparation of Enantiomerically Pure (1R,2R)- and (1S,2S)-2-AminocyclohexanolsBulletin of the Chemical Society of Japan, 1994
- Lipase-catalysed enantioselective acylation of N-protected or unprotected 2-aminoalkan-1-olsJournal of the Chemical Society, Perkin Transactions 1, 1992
- A General Method for the Separation of Enantiomerictrans-2-Substituted CyclohexanolsSynthesis, 1990
- Lipase-catalyzed resolution of chiral 2-amino 1-alcoholsThe Journal of Organic Chemistry, 1987
- Kinetic resolution of racemic .beta.-hydroxy amines by enantioselective N-oxide formationThe Journal of Organic Chemistry, 1985
- A convenient method for obtaining trans-2-aminocyclohexanol and trans-2-aminocyclopentanol in enantiomerically pure formThe Journal of Organic Chemistry, 1985
- Quantitative analyses of biochemical kinetic resolutions of enantiomersJournal of the American Chemical Society, 1982