Enzymatic Preparation of Enantiomerically Pure (1R,2R)- and (1S,2S)-2-Aminocyclohexanols
- 1 April 1994
- journal article
- Published by Oxford University Press (OUP) in Bulletin of the Chemical Society of Japan
- Vol. 67 (4) , 1196-1197
- https://doi.org/10.1246/bcsj.67.1196
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- Asymmetric ring-opening of cyclohexene oxide with trimethylsilyl azide in the presence of titanium isopropoxide/chiral ligandJournal of Organometallic Chemistry, 1988
- A novel and efficient synthesis of (+)- and (−)-trans-2-aminocyclohexanol by enzymatic hydrolysisTetrahedron Letters, 1988
- 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
- Studies on Antibiotics and Related Substances. XVII. Syntheses of trans-2-Aminocyclohexyl-d-glucosaminidesBulletin of the Chemical Society of Japan, 1963