Facile resolution of planar chiral organometallic alcohols with lipase in organic solvents
- 1 January 1990
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 31 (27) , 3895-3896
- https://doi.org/10.1016/s0040-4039(00)97499-9
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Enzymes in organic synthesis : VI scope and enantioselectivity of enzymatic hydrolyses of organosilyl-substituted estersTetrahedron Letters, 1990
- Enzymatic esterification of 1-ferrocenylethanol: An alternate approach to chiral ferrocenyl bis-phosphinesTetrahedron Letters, 1989
- Stereoselective microbial reduction of planar chiral and prochiral organometallic aldehydesBiotechnology Letters, 1989
- 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
- Organometallic substrates of enzymes: Lipase catalysed transesterifications in organic solvents via O-stannyl ethersJournal of Organometallic Chemistry, 1989
- Kinetic resolution of chiral metallocenic aldehydes and alcohols with liver alcohol dehydrogenaseTetrahedron Letters, 1989
- Enantioselective microbial reduction of planar chiral organometallics of synthetic interestJournal of the Chemical Society, Chemical Communications, 1988
- Enantioselective synthesis of chiral benzylic amines. (A stereospecific transamination-alkylation reaction)Tetrahedron Letters, 1986