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140122 ||| eng |
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|a 9789401124447
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| 100 |
1 |
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|a Servi, S.
|e [editor]
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| 245 |
0 |
0 |
|a Microbial Reagents in Organic Synthesis
|h Elektronische Ressource
|c edited by S. Servi
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| 250 |
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|a 1st ed. 1992
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| 260 |
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|a Dordrecht
|b Springer Netherlands
|c 1992, 1992
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| 300 |
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|a X, 490 p
|b online resource
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| 505 |
0 |
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|a Microbial alcohol/aldehyde oxidoreductases in enantioselective conversions -- Stereocontrolled reduction of ?-ketoesters with Geotriehum candidum -- Usefull enzymes from plant cell and organ cultures -- List of Contributors -- List of Participants
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| 505 |
0 |
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|a A kinetic interpretation of acids and alcohols influence on the enantioselectivity in enzyme catalysed resolutions -- Asymmetrized tris(hydroxymethyl)methane and related synthons as new highly versatile chiral building blocks. Chemoenzymatic preparation and synthetic applications -- Oxidations -- A comparative study of chemical versus biological functionalizations of synthetic intermediates -- Enantioselective sulfoxidations catalyzed by chloroperoxidase and horseradish peroxidase -- Use of biooxygenation in fine organic synthesis -- The enzymatic Baeyer-Villiger oxidation -- Beauveria Sulfurescens mediated oxidation of dihydroartemisin derivates -- Reductions -- Comparison of chemical and biochemical reduction methods for the synthesis of (R)-2-hydroxy-4-phenylbutyric acid -- Stereochemical control in microbial reduction -- Approaches to 2-methyl-l-alkanols of high enantiomeric purities via enzyme mediated reactions --
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| 505 |
0 |
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|a Biotransformations applied to the synthesis of vitamins and pharmaceuticals -- Hydrolytic and Proteolytic Enzymes -- A direct route from hydantoins to D-amino acids employing a resting cell biocatalyst with D-hydantoinase and D-carbamoylase activity -- The use of immobilized penicillin G acylase in organic synthesis -- Are proteases suitable tools for the formation of peptide bonds? -- Enzymatic aminolysis, hydrazinolysis and oximolysis reactions -- Microbial and enzymatic transformation of nitriles -- Resolution of racemates with lipases and effect of reaction conditions on enantioselectivity -- Selectivity enhancement of Candida cylindracea lipase: covalent enzyme modification and control of micro-pH -- Lipase catalyzed organic synthesis -- Kinetics and validation of mathematical models of enantioselective transesterification in organicsolvents -- Enzymatic enantioselective ester hydrolysis by carboxylesterase NP --
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| 505 |
0 |
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|a C-C Bond Formation -- Cyclase mediated synthesis of terpenoids -- (R)- and (S)-Cyanohydrins — Their enzymatic synthesis and their reactions -- Chemical-enzymatic synthesis of carbohydrates -- A building block strategy for asymmetric synthesis: the DHAP-aldolases -- Transferase catalyzed synthesis: applications in series of aminoacids and monosaccharides -- Acyloin formation mediated by benzoylformate decarboxylases -- Synthetic Applications -- Organic synthesis via biocatalytic methods — A chemoenzymatic approach to the synthesis of FK506 -- Use of enzymes as catalysts in key reactions leading to the synthesis of optically active natural products and analogues -- New enzymatic methods for the selective functionalization of carbohydrate derivatives -- Efficient synthesis of optically active carbohydrates and other oxygenated compounds through bio-oxidation of chlorinated aromatics -- Chemoenzymatic synthesis of natural products and bioactive compounds --
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| 653 |
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|a Chemistry, Organic
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| 653 |
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|a Bioorganic Chemistry
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| 653 |
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|a Bioorganic chemistry
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| 653 |
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|a Biochemistry
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| 653 |
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|a Organic Chemistry
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| 041 |
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7 |
|a eng
|2 ISO 639-2
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| 989 |
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|b SBA
|a Springer Book Archives -2004
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| 490 |
0 |
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|a Nato Science Series C:, Mathematical and Physical Sciences
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| 028 |
5 |
0 |
|a 10.1007/978-94-011-2444-7
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| 856 |
4 |
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|u https://doi.org/10.1007/978-94-011-2444-7?nosfx=y
|x Verlag
|3 Volltext
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|a 547
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|a 572
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