185493

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Solvent extraction and separation of gallium, indium and thallium with N-benzylaniline.

M M Khosla et al.

Talanta, 21(6), 411-415 (1974-06-01)

A simple and rapid method is proposed for the separation of tervalent gallium, indium and thallium by solvent extraction with N-benzylaniline in chloroform from different concentrations of hydrochloric acid. Thallium and gallium are extracted from 1M and 7.0-7.5M hydrochloric acid

Structure-activity relationships in the formation of amides from substituted N-benzylanilines.

M Ulgen et al.

Xenobiotica; the fate of foreign compounds in biological systems, 24(8), 735-748 (1994-08-01)

1. The in vitro hepatic microsomal metabolism of certain substituted N-benzylanilines was studied in the male hamster to establish the mechanism(s) and process(es) involved in the formation of the corresponding amides. 2. N-Benzyl-2,4,6-trihalogeno, N-benzyl-4-cyano- and N-benzyl-4-nitroanilines were only metabolized by

A UV-visible spectroelectrochemical study of the electropolymerisation of N-benzylaniline.

Malinauskas A and Holze R.

Journal of Solid State Electrochemistry, 3(7-8), 429-436 (1999)

Synthesis and structure-activity relationships of a class of sodium iodide symporter function inhibitors.

Fanny Waltz et al.

ChemMedChem, 6(10), 1775-1777 (2011-07-14)

Synthesis, characterization and catalytic activity of saturated and unsaturated N-heterocyclic carbene iridium(i) complexes.

Yung-Hung Chang et al.

Dalton transactions (Cambridge, England : 2003), (5)(5), 861-867 (2009-01-22)

Both saturated and unsaturated N-benzyl substituted heterocyclic carbene (NHC) iridum(i) complexes were synthesized. The unsaturated carbene complex [(un-NHC-Bn)Ir(CO)(2)Cl] in the cis form was prepared via the carbene transfer from the corresponding silver complex to [Ir(COD)(2)Cl](2) followed by ligand substitution with

Electrochemical polymerization and characterization of N-benzylaniline.

Dong S and Li Z.

Synthetic Metals, 33(1), 93-98 (1989)

Microsomal N- and C-oxidation of 4-substituted N-benzylanilines.

J W Gorrod et al.

Xenobiotica; the fate of foreign compounds in biological systems, 15(12), 1021-1031 (1985-12-01)

Using direct specific analytical techniques microsomal metabolism of N-benzyl-4-substituted anilines has been investigated and found to include both N- and C-oxidation. N-Debenzylation was observed with all substrates and species examined. N-Oxidation usually yielded aryl nitrones, although the N-hydroxy derivative of

de novo design and synthesis of N-benzylanilines as new candidates for VEGFR tyrosine kinase inhibitors.

Masaharu Uno et al.

Organic & biomolecular chemistry, 6(6), 979-981 (2008-03-11)

N-Benzylanilines were designed and synthesized as vascular endothelial growth factor (VEGF)-2 inhibitors using de novo drug design systems based on the X-ray structure of VEGFR-2 kinase domain. Among compounds synthesized, compound showed the most potent inhibitory activity toward VEGFR-2 (KDR)

Identification of a new metabolite after incubation of N-benzylaniline with rabbit liver microsomes.

H M Ali et al.

Journal of chromatography, 202(2), 287-293 (1980-12-19)

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