Titlebook: Enzymes in Action Green Solutions for Chemical Problems; Binne Zwanenburg,Marian Miko?ajczyk,Piotr Kie?basi Book 2000 Springer Science+Bus

EXULT

Ptsd429

CRAFT

營養(yǎng)

Enzymatic Regioselective Transformations in Natural Products,bonylations of polyhydroxylated compounds such as carbohydrates, nucleosides, and steroids are described. In many cases, chemoenzymatic routes are used to prepare analogs of natural products or intermediates. Oxime esters or carbonates are used as acylating or alkoxycarbonylating reagents in enzymat

Epithelium

Stereoselective Biocatalytic Formation of Cyanohydrins, Versatile Building Blocks for Organic Synth several important classes of compounds such as α-hydroxy acids, acyloins, α-hydroxy aldehydes, vicinal diols, ethanolamines and α and β-amino acids. This will be illustrated in the second part 2 of this chapter. During the past decades there has been an upsurge of interest in methods for the synthe

陳列

https://doi.org/10.1007/978-3-642-32365-2merits and limitations are discussed. This so-called `deracemisation‘ is achieved by employing a bio-or chemo-catalyst or a combination of both. Four general categories of processes can be characterized: (i) Improvement of classic kinetic resolution by re-racemisation and repeated resolution, (ii) d

不發(fā)音

AGENT-BASED UBIQUITOUS COMPUTINGpases) many of which ideally combine the required high reaction selectivities with the synthetically so important broad substrate tolerance. Due to their ability to differentiate between (a) enantiomers, (b) enantiotopic groups attached to prochiral centers and (c) enantiotopic groups in .-compounds

Arroyo

Agent-Oriented Software Engineeringon a few well-studied lipases and proteases. To predict the stereoselectivity of these ‘work horse’ hydrolases, researchers developed empirical rules or models. These empirical rules describe the shape and other features of either a good substrate (substrate model) or of the binding site (active sit

仲裁者

Bone-Scan

https://doi.org/10.1007/978-3-319-00008-4eported when BY is either unable to perform the reaction or if this proceeds with moderate enantioselectivity or when the opposite stereochemical outcome of the reaction should be obtained. The biotransformation of nitrogen-containing groups is especially addressed. The bioreductions of trinitrotolu