N-Bromosulphonamides, synthesized via direct bromination of sulphonamides, react with several types of arene substrates in the presence of KSCN to afford aryl thiocyanates. The method appears to be generally applicable to benzenoid substrates with a wide range of substituents, such as N,N-dimethylaniline, p-xylene, anisole, mesitylene and cumene
A general and facile one-pot protocol for the preparation of a broad range of alkyl and aryl isothio...
A direct and straightforward thiocyanation of enamides with NH4SCN under metal-free conditions has b...
Presence of TMSX (X = Cl, Br, I) unleashes the oxidative character of Selectfluor and provides a mil...
An unprecedented transfer of a thiocyanate (−SCN) group from aroyl/acyl isothiocyanate to alkyl or b...
The cyanation of organic compounds is an important and useful process as it directly provides nitril...
A rapid, metal-free and solvent-free (very low loading of solvent in few cases) reaction conditions ...
An efficient and highly selective approach for intermolecular arylthiocyanation/arylselenocyanation ...
n a one-pot procedure, bromineless brominating reagent 1,1′-(ethane-1,2-diyl)dipyridinium bistribrom...
The addition of carbon (Grignard and organolithium reagents) and hydride nucleophiles (Schwartz reag...
In order to synthesize thioamides, Grignard reaction of isothiocyanates was investigated and found t...
International audienceThe practical and mild aerobic oxidative CuCN-mediated cyanation of thiophenol...
This work was supported by the Russian Science Foundation, project # 21-73-10212
For the first time, the crystal structure of a ditribromide reagent 1,1′-(ethane-1,2-diyl)dipyridini...
\(p\)-Tolyl and \(p\)-anisyl isothiocyanates have been condensed with various aromatic hydrocarbons,...
A novel, user-friendly, and convenient method for the synthesis of trisubstituted thioureas of aryla...
A general and facile one-pot protocol for the preparation of a broad range of alkyl and aryl isothio...
A direct and straightforward thiocyanation of enamides with NH4SCN under metal-free conditions has b...
Presence of TMSX (X = Cl, Br, I) unleashes the oxidative character of Selectfluor and provides a mil...
An unprecedented transfer of a thiocyanate (−SCN) group from aroyl/acyl isothiocyanate to alkyl or b...
The cyanation of organic compounds is an important and useful process as it directly provides nitril...
A rapid, metal-free and solvent-free (very low loading of solvent in few cases) reaction conditions ...
An efficient and highly selective approach for intermolecular arylthiocyanation/arylselenocyanation ...
n a one-pot procedure, bromineless brominating reagent 1,1′-(ethane-1,2-diyl)dipyridinium bistribrom...
The addition of carbon (Grignard and organolithium reagents) and hydride nucleophiles (Schwartz reag...
In order to synthesize thioamides, Grignard reaction of isothiocyanates was investigated and found t...
International audienceThe practical and mild aerobic oxidative CuCN-mediated cyanation of thiophenol...
This work was supported by the Russian Science Foundation, project # 21-73-10212
For the first time, the crystal structure of a ditribromide reagent 1,1′-(ethane-1,2-diyl)dipyridini...
\(p\)-Tolyl and \(p\)-anisyl isothiocyanates have been condensed with various aromatic hydrocarbons,...
A novel, user-friendly, and convenient method for the synthesis of trisubstituted thioureas of aryla...
A general and facile one-pot protocol for the preparation of a broad range of alkyl and aryl isothio...
A direct and straightforward thiocyanation of enamides with NH4SCN under metal-free conditions has b...
Presence of TMSX (X = Cl, Br, I) unleashes the oxidative character of Selectfluor and provides a mil...