The microbial reduction of 2-chloro-3-oxoesters
- 30 September 1995
- journal article
- Published by Elsevier in Tetrahedron: Asymmetry
- Vol. 6 (9) , 2199-2210
- https://doi.org/10.1016/0957-4166(95)00294-y
Abstract
No abstract availableKeywords
This publication has 78 references indexed in Scilit:
- A New Alkoxyiodination and Nitratoiodination of α,β-Unsaturated Ketone and Ester Using Iodine-Cerium(IV) Ammonium NitrateChemistry Letters, 1994
- Asymmetric Reduction of Aromatic Ketones. II. An Enantioselective Synthesis of Methyl(2R,3S)-3-(4-Methoxypehnyl)glycidate.CHEMICAL & PHARMACEUTICAL BULLETIN, 1993
- A simplified procedure for the stereospecific transformation of 1,2-diols into epoxidesTetrahedron, 1992
- A practical, highly enantioselective synthesis of the taxol side chain via asymmetric catalysis.The Journal of Organic Chemistry, 1992
- Inscriptions de DelphesBulletin de Correspondance Hellénique, 1991
- Synthesis of 5-[1-hydroxy(or methoxy)-2-bromo(or chloro)ethyl]-2'-deoxyuridines and related halohydrin analogs with antiviral and cytotoxic activityJournal of Medicinal Chemistry, 1989
- Highly Enantioselective Reduction of Ethyl 2-Acyloxy-3-oxobutanoate with Immobilized Baker’s YeastBulletin of the Chemical Society of Japan, 1986
- The use of microorganisms in organic synthesis. I. Microbiological asymmetric reduction of 2-methyl-3-oxobutyrates.CHEMICAL & PHARMACEUTICAL BULLETIN, 1983
- The kinetics and mechanisms of additions to olefinic substances. Part X. Stereochemistry of the chloro- and bromo-hydrins derived from cinnamic acid, and of some derivatives thereofJournal of the Chemical Society, Perkin Transactions 2, 1973
- Chlorination of αβ-unsaturated carbonyl compounds. Part III. Reaction of chlorine with trans-cinnamic acid and the trans-cinnamate ionJournal of the Chemical Society B: Physical Organic, 1968