Chemoenzymatic Synthesis of Both Enantiomers of Fluoxetine
- 1 September 1991
- journal article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 20 (9) , 1603-1606
- https://doi.org/10.1246/cl.1991.1603
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- A new chemoenzymatic enantioselective synthesis of R-(−)-tomoxetine, (R)- and (S)-fluoxetine.Tetrahedron Letters, 1991
- Baker's yeast mediated transformations in organic chemistryChemical Reviews, 1991
- Chapter 3. Antidepressant AgentsPublished by Elsevier ,1989
- Enantioselective and practical syntheses of R- and S-fluoxetinesTetrahedron Letters, 1989
- Asymmetric synthesis of both enantiomers of tomoxetine and fluoxetine. Selective reduction of 2,3-epoxycinnamyl alcohol with Red-AlThe Journal of Organic Chemistry, 1988
- The absolute configurations and pharmacological activities of the optical isomers of fluoxetine, a selective serotonin-uptake inhibitorJournal of Medicinal Chemistry, 1988
- Molecular structure of fluoxetine hydrochloride, a highly selective serotonin-uptake inhibitorJournal of Medicinal Chemistry, 1988
- Enantiomerically Pure Compounds via Chiral OrganoboranesPublished by Springer Nature ,1986
- Asymmetric reductinon of carbonyl compounds by yeast. II. Preparation of optically active α- and β-hydroxy carboxylic acid derivativesAustralian Journal of Chemistry, 1976
- Nuclear magnetic resonance enantiomer regents. Configurational correlations via nuclear magnetic resonance chemical shifts of diastereomeric mandelate, O-methylmandelate, and .alpha.-methoxy-.alpha.-trifluoromethylphenylacetate (MTPA) estersJournal of the American Chemical Society, 1973