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Reaction mechanism of alanine racemase. .

Reaction mechanism of alkaline phosphatase.

Reaction mechanism of aminoacyl-tRNA amidotransferase. For Asp-tRNA amidotransferase , n 2, tRNA tRNA .

Reaction mechanism of asymmetric addition of hydrogen bromide to ethyl trans-cinnamate in the cavity of 3-cyclodextrin

Reaction mechanism of Au-Ag alloy nanoparticle formation.

Reaction Mechanism of Base-Catalyzed Aspartimide Formation

Reaction mechanism of butane oxidation on CNT and phosphorous-doped, pre-oxidized CNT. For details, see text.

Reaction mechanism of CALB

Reaction mechanism of carboxylation of alcohols promoted by DCC.

Reaction mechanism of catalytic hydrogenolysis of diphenylmethane.

Reaction mechanism of ceiiuiase from Trichoderma viride. -giycosidic iinkage.

Reaction mechanism of chitinase from Bacillus sp. -giycosidic iinkage.

Reaction mechanism of chymotrypsin as an example of covalent catalysis. Step I involves attack of the enzyme s active site serine on the peptide bond to be cleaved. In step II, a covalent complex is formed between the enzyme and a portion of the substrate . Step III involves hydrolysis of the enzyme-substrate complex, which releases peptide 2 and completes the reaction.

Reaction mechanism of chymotrypsin.

Reaction mechanism of class IIRNR.

Reaction mechanism of CO2 fixation by RUBISCO. Adapted from http

Reaction mechanism of condensation-curing RTV-2 silicone rubber systems.

Reaction mechanism of copper-amino acid complexation at the Cu -SPE.

Reaction Mechanism of Cyclooctane Oxidation by N-Hydroxylphthalimide

Reaction mechanism of diazonium coupling in poly

Reaction mechanism of dicarbosylated PLA reacting with DGEBA .

Reaction mechanism of diene insertion with a catalyst system based on NdCl3 2 TBP and TIBA , reprinted with permission from Elsevier

Reaction mechanism of DMAT formation catalysed by DMAT synthase

Reaction mechanism of DNA photolyases

Reaction mechanism of dTDP-glucose 4,6-dehydratase as proposed by Allard et al. , The first half of the reaction involves abstraction of a proton from the 4 hydroxyl group, and hydride transfer from C-4 to NAD. In the next step, a proton is removed from the C-5 atom of the sugar, and the C-6 hydroxyl group is protonated and eliminated as water. This yields the 4-keto-5,6-ene intermediate. The product is obtained after hydride transfer from NADH to carbon atom C-6 and protonation of carbon atom C-5



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