Stereoselective microbial reduction of planar chiral and prochiral organometallic aldehydes
- 1 October 1989
- journal article
- research article
- Published by Springer Nature in Biotechnology Letters
- Vol. 11 (10) , 679-684
- https://doi.org/10.1007/bf01044096
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Enzymatic esterification of 1-ferrocenylethanol: An alternate approach to chiral ferrocenyl bis-phosphinesTetrahedron Letters, 1989
- Stereoselectivity of horse liver alcohol dehydrogenase catalyzed oxidoreduction of an organometallic meso diol and the corresponding dialdehydeTetrahedron Letters, 1988
- Biotransformation as a New Method for Preparing Optically Active Organometallic CompoundsaAnnals of the New York Academy of Sciences, 1988
- Asymmetric synthesis catalyzed by chiral ferrocenylphosphine-metal complexesPublished by Walter de Gruyter GmbH ,1988
- Microbial asymmetric reduction of organometallic ketones: Acetylferrocene and (Acetophenone)-tricarbonylchromium.Agricultural and Biological Chemistry, 1988
- Enantioselective synthesis of chiral benzylic amines. (A stereospecific transamination-alkylation reaction)Tetrahedron Letters, 1986
- Microbiological Asymmetric Hydroxylation of 7-Carboxybicyclo[2.2.1]heptane and hept-2-ene and Their Methyl Esters Giving Potentially Useful Chiral Synthons for CyclopentanoidsAgricultural and Biological Chemistry, 1985
- Enantiomeric purity of chiral metal carbonyl complexes using Eu(hfc)3Magnetic Resonance in Chemistry, 1985
- Microbiological asymmetric hydroxylation of 7-carboxybicyclo(2.2.1)heptane and hept-2-ene and their methyl esters giving potentially useful chiral synthons for cyclopentanoids.Agricultural and Biological Chemistry, 1985