A short efficient preparation of (+) and (−)-trans-2-phenylcyclohexanol
- 1 November 1996
- journal article
- research article
- Published by Elsevier in Tetrahedron: Asymmetry
- Vol. 7 (11) , 3107-3108
- https://doi.org/10.1016/0957-4166(96)00409-0
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- Enzymatic resolution of trans-2-arylcyclohexan-1-ols using crude chicken liver esterase (CCLE) as biocatalystTetrahedron: Asymmetry, 1994
- An efficient synthesis of enantiomerically pure trans-2-phenylcyclohexanolTetrahedron Letters, 1994
- Highly Enantioselective, Catalytic Epoxidation of Trisubstituted OlefinsThe Journal of Organic Chemistry, 1994
- Asymmetric Lewis Acid-Dienophile Complexation: Secondary Attraction versus Catalyst PolarizabilityJournal of the American Chemical Society, 1994
- Cyclohexyl-based chiral auxiliariesChemical Reviews, 1992
- 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
- Hydroboration. 80. Preparation of trans-2-phenylcyclopentyl- and trans-2-phenylcyclohexylboronates of very high enantiomeric puritiesThe Journal of Organic Chemistry, 1987
- A new method for the preparation of .gamma.,.delta.-unsaturated ketones via Claisen rearrangementThe Journal of Organic Chemistry, 1985
- Preparation of an optically active prostaglandin intermediate via asymmetric inductionJournal of the American Chemical Society, 1975
- Optically active aromatic chromophores. XI. Circular dichroism studies of some 1-substituted 2-phenylcyclohexanesJournal of the American Chemical Society, 1972