ENANTIOSELECTIVE SYNTHESIS OF MONOFLUORINATED MALONIC ACID MONOESTERS WITH ENZYMES OF MICROBIAL ORIGIN
- 5 October 1984
- journal article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 13 (10), 1811-1814
- https://doi.org/10.1246/cl.1984.1811
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- DL-Threo-.beta.-fluoroaspartate and LD-threo-.beta.-fluoroasparagine: selective cytotoxic agents for mammalian cells in cultureJournal of Medicinal Chemistry, 1982
- Suicide substrates: mechanism-based enzyme inactivatorsTetrahedron, 1982
- Chirally selective synthesis of sugar moiety of nucleosides by chemicoenzymatic approach: L- and D-riboses, showdomycin, and cordycepinJournal of the American Chemical Society, 1981
- Bifunctional chiral synthons via microbiological methods. 1. Optically active 2,4-dimethylglutaric acid monomethyl estersJournal of the American Chemical Society, 1981
- Synthesis of (S)- and (R)-4[(methoxycarbonyl)methyl]-2-azetidinone by chemicoenzymic approachJournal of the American Chemical Society, 1981
- Fluoromevalonate acts as an inhibitor of insect juvenile hormone biosynthesisNature, 1981
- Asymmetric hydrogenation of geminal-substituted vinyl acetatesThe Journal of Organic Chemistry, 1980
- Mechanistic studies with vinylglycine and .beta.-haloaminobutyrates as substrates for cystathionine .gamma.-synthetase from Salmonella typhimuriumBiochemistry, 1979
- Catalytic irreversible inhibition of mammalian ornithine decarboxylase (E.C.4.1.1.17) by substrate and product analogsJournal of the American Chemical Society, 1978