عنوان

Microbial Reagents in Organic Synthesis

شابک

0792319532

شابک

9401050783

شابک

9401124442

شابک

9780792319535

شابک

9789401050784

شابک

9789401124447

شماره

b595052

عنوان اصلي

Microbial Reagents in Organic Synthesis

نام عام مواد

[Book]

نام نخستين پديدآور

edited by Stefano Servi.

محل نشرو پخش و غیره

Dordrecht

نام ناشر، پخش کننده و غيره

Springer Netherlands : Imprint : Springer

تاریخ نشرو بخش و غیره

1992

نام خاص و کميت اثر

(504 pages 2 illustrations)

عنوان فروست

NATO ASI series., Series C,, Mathematical and physical sciences ;, 381.

متن يادداشت

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 --; 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 organic solvents --; Enzymatic enantioselective ester hydrolysis by carboxylesterase NP --; 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 --; 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.

متن يادداشت

Different aspects of biocatalysis are discussed with a view to obtaining products in a practical way using microorganisms and enzymes in catalytic amounts but as if they were organic reagents. A limited number of reactions catalysed by microbial reagents have been examinded according to the following classes: C-C bond formation, including the reaction catalyzed by aldolases, enantiomeric oxynitrilases, and decarboxylases. Oxidations promoted by microorganisms leading to Bayer-Williger-type products and hydroxylation at saturated carbon also includes the production of synthons derived from the microbial oxidation of substituted aromatics of wide synthetic applications. Reductions of carbonyl group with yeasts and other microorganisms, including the factor affecting the stereoselectivity when using all-cell organisms.
Group transfer reactions describes synthetic achievements and theoretical aspects concerning the use of lipases, esterases and acylases. Industrial applications of microbial reagents in the large-scale production of fine chemicals offers validation to the basic research in the field.

عنوان اصلي به زبان ديگر

Proceedings of the NATO Advanced Research Workshop, Sestri Levante, Italy, March 23-27, 1992

موضوع مستند نشده

Microbial metabolism -- Congresses.

موضوع مستند نشده

Organic compounds -- Biotechnology -- Congresses.

موضوع مستند نشده

Organic compounds -- Synthesis -- Congresses.

شماره رده

نشانه اثر

مستند نام اشخاص تاييد نشده

edited by Stefano Servi.

مستند نام اشخاص تاييد نشده

Stefano Servi

نام الکترونيکي

نوع ماده

[Book]

تكميل شده

Y