Lipase/Ruthenium-Catalyzed Dynamic Kinetic Resolution of Hydroxy Acids, Diols, and Hydroxy Aldehydes Protected with a Bulky Group
- 1 June 2001
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 66 (13), 4736-4738
- https://doi.org/10.1021/jo0156417
Abstract
No abstract availableThis publication has 16 references indexed in Scilit:
- Concerted Catalytic Reactions for Conversion of Ketones or Enol Acetates to Chiral AcetatesOrganic Letters, 2000
- The efficient resolution of protected diols and hydroxy aldehydes by lipases: steric auxiliary approach and synthetic applicationsBioorganic & Medicinal Chemistry Letters, 1996
- Dynamic kinetic resolutionTetrahedron: Asymmetry, 1995
- Substrate modification to increase the enantioselectivity of hydrolases. A route to optically-active cyclic allylic alcohols.Tetrahedron: Asymmetry, 1993
- The biocatalytic approach to the preparation of enantiomerically pure chiral building blocksChemical Reviews, 1992
- Pyranose .alpha.-enones provided ready access to functionalized trans-decalins via bis-annulated pyranosides obtained by intramolecular Diels-Alder reactions. A key intermediate for forskolin.The Journal of Organic Chemistry, 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
- Enzymatic preparation of enantiomerically pure and selectively protected 1,2- and 1,3-diolsJournal of the Chemical Society, Chemical Communications, 1991
- Asymmetric transformations catalyzed by enzymes in organic solventsAccounts of Chemical Research, 1990
- General Aspects and Optimization of Enantioselective Biocatalysis in Organic Solvents: The Use of Lipases [New Synthetic Methods (76)]Angewandte Chemie International Edition in English, 1989