Efficient procedures for the large-scale preparation of (1S,2S)-trans-2-methoxycyclohexanol, a key chiral intermediate in the synthesis of tricyclic β-lactam antibiotics
- 31 August 1996
- journal article
- Published by Elsevier in Tetrahedron: Asymmetry
- Vol. 7 (8) , 2247-2250
- https://doi.org/10.1016/0957-4166(96)00279-0
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
- Pig liver acetone powder (PLAP) as biocatalyst: Enantioselective synthesis of trans-2-alkoxycyclohexan-1-olsTetrahedron, 1994
- Synthesis of enantiomerically pure (R)-2-cycloalken-1-ols using highly enantioselective enzymatic transesterificationTetrahedron: Asymmetry, 1993
- A General Method for the Separation of Enantiomerictrans-2-Substituted CyclohexanolsSynthesis, 1990
- Production of Optically Active Esters and Alcohols from Racemic Alcohols by Lipase-Catalyzed Stereoselective Transesterification in Non-Aqueous Reaction SystemThe Journal of Biochemistry, 1989
- Enantiomerically pure cyclohexanols and cyclohexane-1,2-diol derivatives; chiral auxiliaries and substitutes for (–)-8-phenylmenthol. A facile enzymatic routeJournal of the Chemical Society, Chemical Communications, 1989
- Chemical resolution of secondary (±)-alcoholsAustralian Journal of Chemistry, 1966