A facile synthesis of 1<i>H</i>-indazoles featuring a Cu(OAc)<sub>2</sub>-catalyzed N–N bond formation using oxygen as the terminal oxidant is described. The reaction of readily available 2-aminobenzonitriles with various organometallic reagents led to <i>o</i>-aminoaryl N–H ketimine species. The subsequent Cu(OAc)<sub>2</sub>-catalyzed N–N bond formation in DMSO under oxygen afforded a wide variety of 1<i>H</i>-indazoles in good to excellent yields
Indazoles are an important class of nitrogen heterocycles because of their excellent performance in ...
Synthesis of indazolone derivatives, which exhibit diverse biological and pharmaceutical activities,...
Herein, we have reported an efficient Pd-catalyzed C–H functionalization of 2<i>H</i>-indazole at C3...
Substituted 1<i>H</i>-indazoles can be formed from readily available arylimidates and organo azides ...
Cooperative cobalt- and copper-catalyzed C–H activation of imidate esters and oxidative coupling wit...
Herein we report a method for the synthesis of indazoles from readily available 2-aminomethyl-phenyl...
A cyanide-free one-pot procedure was developed to access 2-amino-3-hydroxy-3<i>H</i>-indoles, which ...
Cooperative cobalt- and copper-catalyzed C-H activation of imidate esters and oxidative coupling wit...
A novel and efficient method for the one-pot synthesis of 2<i>H</i>-indazole from readily available ...
A novel and efficient method for the one-pot synthesis of 2<i>H</i>-indazole from readily available ...
A novel and efficient method for the one-pot synthesis of 2<i>H</i>-indazole from readily available ...
A novel and efficient method for the one-pot synthesis of 2<i>H</i>-indazole from readily available ...
A rhodium(III)-catalyzed intermolecular C–H amination of ketoxime and iodobenzene diacetate-enabled...
The iridium-catalyzed dehydrogenative cyclization of 2-aminobiphenyls proceeds smoothly in the prese...
A simple, practical, and highly efficient synthesis of pyrazoles and indazoles via copper-catalyzed ...
Indazoles are an important class of nitrogen heterocycles because of their excellent performance in ...
Synthesis of indazolone derivatives, which exhibit diverse biological and pharmaceutical activities,...
Herein, we have reported an efficient Pd-catalyzed C–H functionalization of 2<i>H</i>-indazole at C3...
Substituted 1<i>H</i>-indazoles can be formed from readily available arylimidates and organo azides ...
Cooperative cobalt- and copper-catalyzed C–H activation of imidate esters and oxidative coupling wit...
Herein we report a method for the synthesis of indazoles from readily available 2-aminomethyl-phenyl...
A cyanide-free one-pot procedure was developed to access 2-amino-3-hydroxy-3<i>H</i>-indoles, which ...
Cooperative cobalt- and copper-catalyzed C-H activation of imidate esters and oxidative coupling wit...
A novel and efficient method for the one-pot synthesis of 2<i>H</i>-indazole from readily available ...
A novel and efficient method for the one-pot synthesis of 2<i>H</i>-indazole from readily available ...
A novel and efficient method for the one-pot synthesis of 2<i>H</i>-indazole from readily available ...
A novel and efficient method for the one-pot synthesis of 2<i>H</i>-indazole from readily available ...
A rhodium(III)-catalyzed intermolecular C–H amination of ketoxime and iodobenzene diacetate-enabled...
The iridium-catalyzed dehydrogenative cyclization of 2-aminobiphenyls proceeds smoothly in the prese...
A simple, practical, and highly efficient synthesis of pyrazoles and indazoles via copper-catalyzed ...
Indazoles are an important class of nitrogen heterocycles because of their excellent performance in ...
Synthesis of indazolone derivatives, which exhibit diverse biological and pharmaceutical activities,...
Herein, we have reported an efficient Pd-catalyzed C–H functionalization of 2<i>H</i>-indazole at C3...