In its formation by the oxidation of thiocarbanilide by bromine in alcohol. Hugershoff's thiadiazole has been shown to be preceded by the formation of tetraphenylformamidine monosulphide which has been isolated as its hydrobromide. Chemistry of this compound has been investigated
3,5-Diaryl (or alkylaryl)-imino-1,2,4-dithiazolidines on being allowed to react with aromatic primar...
Like their aryl homologues the hydrogen halides of the alkyl-substituted thiurets react with the aro...
3,5-Diaryl (or alkylaryl)-imino-1,2,4-dithiazolidines on being allowed to react with aromatic primar...
Hugershoff's base cannot be represented by the thiodiazole structure, initially assigned to it. An a...
Analogous to the oxidation of phenylthiocarbamide to Hector's base1, the final product of oxidation ...
Analogous to the oxidation of phenylthiocarbamide to Hector's base1, the final product of oxidation ...
Bromine reacts in an indifferent solvent medium with thiocarbarnide or its oxidation product, the ‘f...
Evidence is adduced to controvert the general belief that unstable disulphides of the formamidine ty...
Sulphur monochloride reacts in an inert solvent medium with thiocarbamide and thiocarbanilide formin...
Oxidation of thiobenzamide and 4-methyl thiobenzamide with iodine has been investigated. The pattern...
The supposed disulphide oxidation product of tetramethyithiocarbamide has been shown to be derived c...
Hydrogen peroxide oxidation of certain symmetrical diarylthiocarbamides in alcoholic medium has been...
Oxidation of 1-tert.butyl-3-phenylthiocarbamide has been investigated. The general course of the rea...
Oxidation of 1-tert.butyl-3-phenylthiocarbamide has been investigated. The general course of the rea...
Oxidation of 1-tert.butyl-3-phenylthiocarbamide has been investigated. The general course of the rea...
3,5-Diaryl (or alkylaryl)-imino-1,2,4-dithiazolidines on being allowed to react with aromatic primar...
Like their aryl homologues the hydrogen halides of the alkyl-substituted thiurets react with the aro...
3,5-Diaryl (or alkylaryl)-imino-1,2,4-dithiazolidines on being allowed to react with aromatic primar...
Hugershoff's base cannot be represented by the thiodiazole structure, initially assigned to it. An a...
Analogous to the oxidation of phenylthiocarbamide to Hector's base1, the final product of oxidation ...
Analogous to the oxidation of phenylthiocarbamide to Hector's base1, the final product of oxidation ...
Bromine reacts in an indifferent solvent medium with thiocarbarnide or its oxidation product, the ‘f...
Evidence is adduced to controvert the general belief that unstable disulphides of the formamidine ty...
Sulphur monochloride reacts in an inert solvent medium with thiocarbamide and thiocarbanilide formin...
Oxidation of thiobenzamide and 4-methyl thiobenzamide with iodine has been investigated. The pattern...
The supposed disulphide oxidation product of tetramethyithiocarbamide has been shown to be derived c...
Hydrogen peroxide oxidation of certain symmetrical diarylthiocarbamides in alcoholic medium has been...
Oxidation of 1-tert.butyl-3-phenylthiocarbamide has been investigated. The general course of the rea...
Oxidation of 1-tert.butyl-3-phenylthiocarbamide has been investigated. The general course of the rea...
Oxidation of 1-tert.butyl-3-phenylthiocarbamide has been investigated. The general course of the rea...
3,5-Diaryl (or alkylaryl)-imino-1,2,4-dithiazolidines on being allowed to react with aromatic primar...
Like their aryl homologues the hydrogen halides of the alkyl-substituted thiurets react with the aro...
3,5-Diaryl (or alkylaryl)-imino-1,2,4-dithiazolidines on being allowed to react with aromatic primar...
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