Add to ORKG[[abstract]]A method for the regioselective synthesis of 3-unsubstituted 1-alkyl-1H-indazoles, starting with 2-halobenzonitriles and N-alkylhydrazines, is described. The two-step reaction pathway proceeds through the intermediacy of 1-alkyl-3-amino-1H-indazoles followed by reductive deamination
A one-pot–three-step method has been developed for the conversion of oxazolino-2<i>H</i>-indazoles i...
A procedure has been developed for synthesis of 2-alkenyl-2H-indazoles starting from 2-(2-carbonylme...
A convenient and efficient strategy has been devised to access 3-amino-2H-indazole derivatives in tw...
International audienceA set of variously substituted indazoles and hetero-aromatic derivatives were ...
A novel and efficient method for the one-pot synthesis of 2<i>H</i>-indazole from readily available ...
An operationally simple and efficient one-pot synthesis of 2<i>H</i>-indazoles from commercially ava...
The development of a novel selective synthesis of 3-amino-2H-indazoles from readily available 2-halo...
The indazole scaffold represents a promising pharmacophore, commonly incorporated in a variety of th...
Methodology of alkylation of aromatic amines using 1H-indazoles as synthetic auxiliaries is reported
Methodology of alkylation of aromatic amines using 1H-indazoles as synthetic auxiliaries is repo...
Methodology of alkylation of aromatic amines using 1H-indazoles as synthetic auxiliaries is reporte
Methodology of alkylation of aromatic amines using 1H-indazoles as synthetic auxiliaries is reporte
The synthesis of 2,6-bis-hydrazonopyridines from 2,6-bis-hydrazinopyridine and the conversion of the...
An efficient route to substituted 1-aryl-1H-indazoles has been developed and optimized. The method i...
The 1<i>H</i>-indazole skeleton can be constructed by a [3 + 2] annulation approach from arynes and ...
A one-pot–three-step method has been developed for the conversion of oxazolino-2<i>H</i>-indazoles i...
A procedure has been developed for synthesis of 2-alkenyl-2H-indazoles starting from 2-(2-carbonylme...
A convenient and efficient strategy has been devised to access 3-amino-2H-indazole derivatives in tw...
International audienceA set of variously substituted indazoles and hetero-aromatic derivatives were ...
A novel and efficient method for the one-pot synthesis of 2<i>H</i>-indazole from readily available ...
An operationally simple and efficient one-pot synthesis of 2<i>H</i>-indazoles from commercially ava...
The development of a novel selective synthesis of 3-amino-2H-indazoles from readily available 2-halo...
The indazole scaffold represents a promising pharmacophore, commonly incorporated in a variety of th...
Methodology of alkylation of aromatic amines using 1H-indazoles as synthetic auxiliaries is reported
Methodology of alkylation of aromatic amines using 1H-indazoles as synthetic auxiliaries is repo...
Methodology of alkylation of aromatic amines using 1H-indazoles as synthetic auxiliaries is reporte
Methodology of alkylation of aromatic amines using 1H-indazoles as synthetic auxiliaries is reporte
The synthesis of 2,6-bis-hydrazonopyridines from 2,6-bis-hydrazinopyridine and the conversion of the...
An efficient route to substituted 1-aryl-1H-indazoles has been developed and optimized. The method i...
The 1<i>H</i>-indazole skeleton can be constructed by a [3 + 2] annulation approach from arynes and ...
A one-pot–three-step method has been developed for the conversion of oxazolino-2<i>H</i>-indazoles i...
A procedure has been developed for synthesis of 2-alkenyl-2H-indazoles starting from 2-(2-carbonylme...
A convenient and efficient strategy has been devised to access 3-amino-2H-indazole derivatives in tw...