Cantitate/Preț
Produs

Enzymes as Catalysts in Organic Synthesis: Nato Science Series C:, cartea 178

Editat de Manfred P. Schneider
en Limba Engleză Hardback – 30 iun 1986

Toate formatele și edițiile

Toate formatele și edițiile Preț Express
Paperback (1) 119873 lei  43-57 zile
  SPRINGER NETHERLANDS – 12 feb 2012 119873 lei  43-57 zile
Hardback (1) 120478 lei  43-57 zile
  SPRINGER NETHERLANDS – 30 iun 1986 120478 lei  43-57 zile

Din seria Nato Science Series C:

Preț: 120478 lei

Preț vechi: 146924 lei
-18% Nou

Puncte Express: 1807

Preț estimativ în valută:
23057 23950$ 19152£

Carte tipărită la comandă

Livrare economică 03-17 februarie 25

Preluare comenzi: 021 569.72.76

Specificații

ISBN-13: 9789027722676
ISBN-10: 9027722676
Pagini: 440
Ilustrații: XIV, 422 p.
Dimensiuni: 155 x 235 x 29 mm
Greutate: 0.79 kg
Ediția:1986
Editura: SPRINGER NETHERLANDS
Colecția Springer
Seria Nato Science Series C:

Locul publicării:Dordrecht, Netherlands

Public țintă

Research

Cuprins

Lectures.- Baker’s yeast mediated preparation of carbohydrate-like chiral synthons.- Alcohol dehydrogenase catalysed oxidoreduction reactions in organic chemistry.- On the use of viologen dyes for stereospecific bioreduction.- Approaches to chiral building blocks for natural product synthesis.- Use of microorganisms for the resolution of synthetically useful bicyclo[ 3.2.0] hept-2-en-6-ones.- The scope of biocatalysts in organic chemical processing.- Enantioselective synthesis of biologically active cyclopentanoids via enzyme catalysed asymmetric reactions.- Creation of novel chiral synthons with pig liver esterase: application to natural product synthesis and the substrate recognition.- Application of microbial transformations in the total synthesis of natural products.- Approaches to chiral building blocks for natural products synthesis.- Synthesis of enantiomerically pure unnatural compounds via non-biomimetic homoaldol reactions.- Aldolases as catalysts in organic synthesis.- Immobilised redox enzymes and their use as catalysts for fine chemical synthesis.- Applications of microbes and microbial enzymes in environmental control and organic synthesis.- Synthesis of chirally labelled substrates using enzymes.- Synthesis of L-amino acids by isolated enzymes and microorganisms.- Development of an enzyme reactor for food chemistry.- Preparation and properties of semisynthetic flavoenzymes.- The study and redesign of enzymes by protein engineering.- Evolutionary guidance and the engineering of enzymes.- Posters.- Baker’s yeast mediated synthesis of protected ?-hydroxyaldehydes.- Enantioselective PLE-catalyzed hydrolysis of meso-dimethyl tetrahydrophthalate on a 100 mole scale — protection of the enzyme by addition of bovine serum albumin.- Enantio- anddiastereoselectivity of microsomal epoxide hydrolase: potential applications to the preparation of non-racemic epoxides and diols.- Efficient enzymic production of enantiomerically pure amino acids.- Biohydroxylation of non activated carbon atoms. A model for the hydroxylation site of the fungus beauveria sulfurescens.- “Sterols Bioconversions in systems with an organic phase”.- Second-generation biocatalysis.- Round-table discussions.- List of contributors.