Azo compounds, both symmetrical and unsymmetrical are cleaved to amine/s by using Raney nickel and ammonium formate or formic acid in methanol at room temperature. The reductive cleavage is very fast, clean, cost effective and high yielding as compared to earlier methods and many other functionality such as -OH, -CH3 -OCH3, -COOH, -COCH3 and halogen remained unaffected
A facile method for a mild single pot reductive cleavage of 1,2-oxazines to γ-hydroxy ketones was de...
A facile method for a mild single pot reductive cleavage of 1,2-oxazines to γ-hydroxy ketones was de...
Azo compounds are conveniently reduced to either partially reduced hydrazo compounds or completely r...
Azo compounds, both symmetric and unsymmetric, are cleaved to amine(s) by using commercial zinc dust...
Azo compounds, both symmetrically and unsymmetrically substituted, are reduced to the corresponding ...
Addition of triethylammonium formate followed by commercial zinc dust to a solution of, azo compound...
Azo compounds are reduced to corresponding anilines with zinc dust in the presence of ammonium chlor...
Addition of ammonium acetate followed by commercial zinc dust to the solution of azo compounds in me...
192-195Addition of ammonium acetate followed by commercial zinc dust to the solution of azo compou...
Azo compounds, both symmetric and asymmetric, were chemoselectively reduced to the corresponding ami...
Abstract Azo compounds, both symmetric and asymmetric, were chemoselectively reduced to the correspo...
Magnesium/triethylammonium formate is a convenient reagent for the reduction of aromatic nitro compo...
A convenient, mild and simple procedure, employing sodium cyanoborohydride in the presence of either...
A convenient, mild and simple procedure, employing sodium cyanoborohydride in the presence of either...
A convenient, mild and simple procedure, employing sodium cyanoborohydride in the presence of either...
A facile method for a mild single pot reductive cleavage of 1,2-oxazines to γ-hydroxy ketones was de...
A facile method for a mild single pot reductive cleavage of 1,2-oxazines to γ-hydroxy ketones was de...
Azo compounds are conveniently reduced to either partially reduced hydrazo compounds or completely r...
Azo compounds, both symmetric and unsymmetric, are cleaved to amine(s) by using commercial zinc dust...
Azo compounds, both symmetrically and unsymmetrically substituted, are reduced to the corresponding ...
Addition of triethylammonium formate followed by commercial zinc dust to a solution of, azo compound...
Azo compounds are reduced to corresponding anilines with zinc dust in the presence of ammonium chlor...
Addition of ammonium acetate followed by commercial zinc dust to the solution of azo compounds in me...
192-195Addition of ammonium acetate followed by commercial zinc dust to the solution of azo compou...
Azo compounds, both symmetric and asymmetric, were chemoselectively reduced to the corresponding ami...
Abstract Azo compounds, both symmetric and asymmetric, were chemoselectively reduced to the correspo...
Magnesium/triethylammonium formate is a convenient reagent for the reduction of aromatic nitro compo...
A convenient, mild and simple procedure, employing sodium cyanoborohydride in the presence of either...
A convenient, mild and simple procedure, employing sodium cyanoborohydride in the presence of either...
A convenient, mild and simple procedure, employing sodium cyanoborohydride in the presence of either...
A facile method for a mild single pot reductive cleavage of 1,2-oxazines to γ-hydroxy ketones was de...
A facile method for a mild single pot reductive cleavage of 1,2-oxazines to γ-hydroxy ketones was de...
Azo compounds are conveniently reduced to either partially reduced hydrazo compounds or completely r...