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Azide binding to native laccase. A

Azide clock method for determining arylnitrenium ion reaction rate constants.

Azide cycloadditions with alkenes. Strained systems react extremely rapidly.

Azide displacement in a disaccharidic 3,3 -diiriflaie having the D-altro,D-altro configuration.

Azide displacements in the unsymmetrical, 3,2 -ditriflate having the u-altro,D-gluco configuration.

Azide inclusion within the cylindrical bis-tren macrobicycle 19-6H.

Azide rescue of an acid base catalyst mutant of a retaining b-glycosidase. R

Azide stacking for salts having small cations .

Azide-alkine click chemistry for the synthesis of three-arm-star functionalized PIBs.

Azide-functionalized F-label for conjugation with alkyne-containing peptides.

Azides by ring opening of epoxides

Azides by ring opening of meso-epoxides

Azides tested for the hydroazidation of 4-phenylbut-1 -ene 3p

Azido derivatives of sugars can be used as monomers for glycan and carbohydrate synthesis by cells. Such modifications can be probed using click chemistry or Staudinger ligation reactions.

Azido group as a conformation-directing element in 4-azidoproline containing polyprolines.

Azido-2, 3 -dideoxynucleosides

Azido-3-chiorobenzyi for catch-and-release purification.

Azido-benzyloxy -4-oxo-3,4-dihydro-l,2,3-benzotriazine .

Azido-sialic acid-containing glycans can be labeled in vivo with biotin-PEG-phosphine using the Staudinger ligation reaction, which forms an amide bond.

Azido-substituted pyrimidines

Azidoacridine potential energy surface portion corresponding to rotations about the N1C4 bond at the B3LYP 6-3IG level energies are given with respect to potential energy surface minima ,

Azidoarylation of alkenes towards the synthesis of oxindoles

Azidoethyl

Azidonitration and azidophenylselenation.

Azidonitration for the preparation of chondroitin sulfate disaccharides.



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