Kinetic resolution of (1RS,2SR)-2-(hydroxymethyl)cyclopentanol by a biocatalytic transesterification using lipase PS
- 1 April 1994
- journal article
- Published by Elsevier in Tetrahedron: Asymmetry
- Vol. 5 (4), 751-754
- https://doi.org/10.1016/0957-4166(94)80038-3
Abstract
No abstract availableThis publication has 12 references indexed in Scilit:
- Kinetic resolution of acyclic 1,2-diols using a sequential lipase-catalyzed transesterification in organic solventsThe Journal of Organic Chemistry, 1994
- Kinetic resolution of aliphatic 1,2-diols by a lipase-catalyzed sequential acetylationTetrahedron Letters, 1993
- Asymmetric conjugate addition of organometallic reagents to chiral α, β-unsaturated estersTetrahedron: Asymmetry, 1991
- Enzymes in Organic Synthesis, 8. Synthesis of enantiomerically pure prostaglandin intermediates by enzymatic transesterification of (1S*,5R*,6R*,7R*)-(±)-7-hydroxy-6-hydroxymethyl-2-oxabicyclo[3.3.0]octan-3-oneEuropean Journal of Organic Chemistry, 1991
- Lipase-catalyzed transesterification of meso-cyclopentane diolsTetrahedron, 1991
- Development of a New Six-Membered Chelating Chiral [Bisphosphine] rhodium Catalyst and Efficient Asymmetric Hydrogenation of (Z)-2-Acetamidocinnamic Acid1Synlett, 1991
- Quantitative analyses of biochemical kinetic resolutions of enantiomersJournal of the American Chemical Society, 1982
- Synthesis of some organotins containing the cyclopentane ringJournal of Organometallic Chemistry, 1977
- Selective reductions. XII. Explorations in some representative applications of aluminum hydride for selective reductionsJournal of the American Chemical Society, 1968
- Die Reduktion von β‐Keto‐carbonsäureestern mit LithiumaluminiumhydridEuropean Journal of Organic Chemistry, 1951