Titlebook: Biotransformations; Kurt Faber Book 1999 Springer-Verlag Berlin Heidelberg 1999 Amino acid.Angewandte Midrobiologie.Bioprze?technik.Biotec

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https://doi.org/10.1007/978-94-015-9765-4s robust catalysts for the epoxidation of a wide range of electron-poor alkenes, such as .-substituted .-unsaturated ketones. The optically active epoxides so formed may be transformed into heterocyclic compounds, polyhydroxylated materials and biologically active compounds such as diltiazem and taxol side chain.

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Microbial Models for Drug Metabolism,hnical methods for developing microbial models. Emphasis is laid on the potential for selected microorganisms to mimic all patterns of mammalian biotransformations and to provide preparative methods for structural identification and toxicological and pharmacological studies of drug metabolites.

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Pablo Fernández de Casadevante Mayordomoermediate in aqueous medium. Thus, if optically active compounds can be prepared via this type of reaction, it would be a very characteristic biotransformation, as compared to ordinary organic reactions. An enzyme isolated from a specific strain of . catalyzes the asymmetric decarboxylation of .-ary

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The Primacy of the Constitution,ion, the decomposition of cyanohydrins. This biotransformation (in the synthesis direction) can generate a product with a new chiral centre which possesses geminal difunctionality, i.e. a hydroxyl and nitrile moiety at a single carbon atom, and which also represents a versatile synthetic intermediat

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Neurolaw: Challenges and Opportunities,more conventional forms of organic reactions. Using these specificities of the enzymes, many useful compounds have been enzymatically produced. Compounds possessing C3- and C4-units with additional functional groups are promising materials for the synthesis of various useful compounds. In particular

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