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O-Aminobenzenethiol

The condensation of o-aminobenzenethiol with pyridine-2,6-dicarbaldehyde does not form the corresponding Schiff base but a polyheterocyclic compound which behaves as a tridentate ligand towards nickel(II).2365 In contrast the reaction of 2-(2-pyridyl)benzothiazoline with nickel(II) results in the opening of the heterocyclic ring and in the formation of a Schiff base ligand which coordinates to nickel(II) as a mononegative tridentate ligand.2366,2367... [Pg.198]

Neutralization of an alcoholic solution of o-aminobenzenethiol (99) with a slight deficiency of... [Pg.1247]

Stephens WD, Field L (1959) A seven-membered heterocycle from o-aminobenzenethiol and chalcone. J Org Chem 24 1576... [Pg.88]

Chelate amino complexes (V Y = NH, Z = 0,S) were obtained from [7T-C5H5Co(CO)l2] with o-aminophenols and o-aminobenzenethiols (255). Related complexes are obtained from [Rh(CO)2Cl]2 with the latter ligands... [Pg.118]

Fe3(CO)[2 reacts with o-aminobenzenethiol in boiling cyclohexane to form the nitrogen- and sulfur-bridged complex (XII), through loss of hydrogen from both the sulfur and nitrogen atoms (338). [Pg.121]

The pyrolysis of a number of benzothiazolines, which were prepared by the reaction of o-aminobenzenethiols with ketones, have been investigated by Elderfield and McClenachan . The first-order rate coefficients were estimated by measure-... [Pg.725]

Condensation of o-aminobenzenethiol 547 with 1 in dimethyl sulfoxide gave the phenothiazinone 550 (76JCS(P1)1146, 83S933,... [Pg.107]

Dichloroquinoxaline has been converted into a number of polycyclic derivatives by reaction with o-disubstituted benzenes. Thus reaction with o-phenylenediamines gives tetraazanaphthacenes (17), and the corresponding reaction with 2,3-diaminoquinoxaline gives fluorubin derivatives (18). Quinoxalino[2,3-h]benzothiazine derivatives (19) result from the reaction of dichloroquinoxaline and o-aminobenzenethiol and... [Pg.170]

Cleavage of aryl esters. Aryl acetates, benzoates, pivalates, and tosylates are cleaved under nonhydrolytic conditions (PhSH, K2CO, NMP reflux) alkyl esters are less reactive. o-Aminobenzenethiol is also useful for this purpose. [Pg.23]

The Mn compounds, derived from the terdentate O—N—O or S—N—O donor set Schiff base ligands obtained from the condensation of both substituted " and unsubstituted " o-hydroxyan-iline, anthranilic acid " or o-aminobenzenethiol " with various salicylaldehyde residues, have the... [Pg.65]

Mdssbauer spectra, 1255 acetylacetonate, 1236 o-alanine, 1226 alkyl cyanides, 1209 amines, 1210 aromatic, 1210 hexamine, 1210 monodentate aromatic, 1212 polyethyleneamine, 1211 pyridine, 1211 amino acids, 1238 o-aminobenzenethiol, 1247 2-aminomethylpyridine, 1226 6-amino-2-methylquinoline, 1213 amminepentacyano-hydrolysis, 1206 arsenic ligands, 1233 monodentate, 1233 polydentate, 1234... [Pg.1292]

This reaction has been modified for preparing oxazole, thiazole, and perimidine derivatives from the condensation of the corresponding o-aminophenol, o-aminobenzenethiol, and 1,8-naphthalenediamine with ketones. ... [Pg.2198]


See other pages where O-Aminobenzenethiol is mentioned: [Pg.148]    [Pg.176]    [Pg.268]    [Pg.134]    [Pg.928]    [Pg.370]    [Pg.201]    [Pg.463]    [Pg.538]    [Pg.97]    [Pg.97]    [Pg.331]    [Pg.332]    [Pg.928]    [Pg.201]    [Pg.3655]    [Pg.6053]    [Pg.124]    [Pg.245]    [Pg.97]    [Pg.97]    [Pg.331]    [Pg.332]    [Pg.245]    [Pg.783]   
See also in sourсe #XX -- [ Pg.371 ]




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Aminobenzenethiols

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