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Pyridoxine and its glycosides prepared by enzymatic reactions

Pyridoxine phosphate-catalyzed transamination and decarho lation.

Pyridtnium cross-links and N-telopeptides of type I collagen. Cross-links occur at two intermolecular sites in the collagen fibril

Pyridyl amine ligands used in combination with Fe or Mn.

Pyridyl analogs closely mimic the carboxyl of proline.

Pyridyl group assisted halogenation

Pyridyl ketene generated by laser flash photolysis in acetonitrile, and trapping by n-butylamine investigated by time-resolved IR measurements .

Pyridyl organometallic reagents and pyridine V-oxidcs as a plausible replacement

Pyridyl sulfoxide as phase transfer catalyst in the 8, 2 reactions of alkyl halides

Pyridyl-benzimidazole based ligand LI used to prepare hetero-trinuclear chromium erbium complexes.

Pyridyl-containing template molecules ,

Pyridylacryloylamino derivatives

Pyridylidene tautomers of 2,2 -bipyridine .

Pyridylsulfones in Julia-Kocienski reactions.

Pyridylsulfones in Tnlia-Korienski reactions.

Pyridyne was postulated as an intermediate in the gas-phase pyrolysis of 107, finally forming 108. Direct proof for the existence of this species has not yet been achieved. The above reaction scheme for the photolysis of 107 in a nitrogen matrix at 13 K

Pyrimidin-part of vitamin Bi-molecule illustration of input

Pyrimidine 5 -nucleotidase assay in undialyzed human erythrocyte lysate obtained by 1

Pyrimidine and Purine Bases

Pyrimidine antibacteriai agents.

Pyrimidine antifungai agents.

Pyrimidine antitumor agents.

Pyrimidine antivirai agents.

Pyrimidine bases are subject to nucleophilic displacement reactions primarily at the C-4 and C-6

Pyrimidine bases are subject to nucleophilic displacement reactions primarily at the C-4 and C-6 positions.



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