Synthesis of optically active 2-sila-1,3-propanediols derivatives by enzymatic transesterification.
- 1 October 1991
- journal article
- Published by Elsevier BV in Tetrahedron Letters
- Vol. 32 (44), 6325-6326
- https://doi.org/10.1016/0040-4039(91)80159-4
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Simple Preparation of the Optically Active γ-Hydroxy Vinylstannanes Using Lipase-Catalyzed HydrolysisChemistry Letters, 1991
- An efficient preparation of the optically active γ -hydroxy stannanes using lipase-catalyzed hydrolysisTetrahedron Letters, 1990
- Enzymes in organic synthesis : VI scope and enantioselectivity of enzymatic hydrolyses of organosilyl-substituted estersTetrahedron Letters, 1990
- Nucleophilic catalysis of organosilicon substitution reactionsOrganometallics, 1989
- Organometallic substrates of enzymes: Lipase catalysed transesterifications in organic solvents via O-stannyl ethersJournal of Organometallic Chemistry, 1989
- Oxime esters as novel irreversible acyl transfer agents for lipase catalysis in organic mediaJournal of the Chemical Society, Chemical Communications, 1989
- Lipase-catalyzed irreversible transesterifications using enol esters as acylating reagents: preparative enantio- and regioselective syntheses of alcohols, glycerol derivatives, sugars and organometallicsJournal of the American Chemical Society, 1988
- Alkylations en absence de solvant organique. Effets d'addition d'oxydes mineraux et de sels d'ammonium—IITetrahedron, 1983