Lipase-mediated diastereoselective and enantioselective acetylations of 3-substituted cyclohexanols
- 12 February 1998
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 39 (7) , 635-638
- https://doi.org/10.1016/s0040-4039(97)10705-5
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- Enantioselective synthesis through enzymatic asymmetrizationTetrahedron, 1996
- Lipase-Supported Synthesis of Biologically Active CompoundsChemical Reviews, 1995
- Lipase-Mediated Kinetic Separation of a Diastereomeric Mixture of 4-tert-ButylcyclohexanemethanolSynthesis, 1995
- Catalytic asymmetric Michael addition of nitroalkane to enone and enalTetrahedron Letters, 1994
- trans‐2‐tert‐Butylcyclohexanol, a Simple Selectively Optimized Cyclohexanol AuxiliaryAngewandte Chemie International Edition in English, 1992
- A rule to predict which enantiomer of a secondary alcohol reacts faster in reactions catalyzed by cholesterol esterase, lipase from Pseudomonas cepacia, and lipase from Candida rugosaThe Journal of Organic Chemistry, 1991
- Pheromone synthesis, CXI. An enzyme-mediated synthesis of both enantiomers of seudenol and 1-methyl-2-cyclohexen-1-ol, the aggregation pheromones ofDendroctonus pseudotsugaeEuropean Journal of Organic Chemistry, 1988
- Enantioselective conjugate addition of rationally designed chiral cuprate reagents to 2-cycloalkenonesJournal of the American Chemical Society, 1986
- trans-2-Phenylcyclohexanol. A powerful and readily available chiral auxiliaryThe Journal of Organic Chemistry, 1985
- The Enantioselective Michael Addition of Thiols to Cycloalkenones by Using (2S, 4S)-2-Anilinomethyl-1-ethyl-4-hydroxypyrrolidine as Chiral CatalystBulletin of the Chemical Society of Japan, 1982