The nitro group in aliphatic and aromatic nitro compounds, which also contain reducible substituents such as alkenes, nitriles, carboxylic acids, phenols, halogens, esters, etc., is selectively and rapidly reduced at room temperature to the corresponding amine in good yield by employing hydrazinium monoformate in the presence of magnesium powder. It was observed that, hydrazinium monoformate is more effective than hydrazine or formic acid or ammonium formate and reduction of the nitro group occurs without hydrogenolysis in the presence of low-cost magnesium compared to expensive metals like palladium, platinum, ruthenium, etc
Azo compounds are conveniently reduced to either partially reduced hydrazo compounds or completely r...
A variety of functionalized alkyl and aryl primary amines have been prepared from corresponding azid...
Aliphatic and aromatic nitro compounds are selectively and rapidly reduced to their corresponding am...
The reduction of nitro compounds, both aliphatic and aromatic into corresponding amines has been ach...
Hydrazine aided catalytic transfer hydrogenation has been employed for the reduction of both aliphat...
The nitro group in aliphatic and aromatic nitro compounds also containing reducible substituents suc...
1315-1318The nitro group in aromatic nitro compounds containing reducible substituents such as meth...
2882-2884The reduction of nitro compounds, both aliphatic and aromatic into corresponding amines ha...
The nitro group in aliphatic and aromatic nitro compounds also containing. reducible substituents su...
180-183The nitro group in aliphatic and aromatic nitro compounds also containing, reducible substit...
Aromatic nitro compounds were chemoselectively reduced to the corresponding amines using recyclable ...
Removal of some commonly used protecting groups in peptide synthesis by catalytic transfer hydrogena...
Azo compounds are conveniently reduced to hydrazo compounds by using commercial zinc dust and hydraz...
The reduction of azo compounds with magnesium powder as catalyst in the presence of ammonium chlorid...
Various aldoximes and ketoximes were selectively reduced to the corresponding amines by catalytic tr...
Azo compounds are conveniently reduced to either partially reduced hydrazo compounds or completely r...
A variety of functionalized alkyl and aryl primary amines have been prepared from corresponding azid...
Aliphatic and aromatic nitro compounds are selectively and rapidly reduced to their corresponding am...
The reduction of nitro compounds, both aliphatic and aromatic into corresponding amines has been ach...
Hydrazine aided catalytic transfer hydrogenation has been employed for the reduction of both aliphat...
The nitro group in aliphatic and aromatic nitro compounds also containing reducible substituents suc...
1315-1318The nitro group in aromatic nitro compounds containing reducible substituents such as meth...
2882-2884The reduction of nitro compounds, both aliphatic and aromatic into corresponding amines ha...
The nitro group in aliphatic and aromatic nitro compounds also containing. reducible substituents su...
180-183The nitro group in aliphatic and aromatic nitro compounds also containing, reducible substit...
Aromatic nitro compounds were chemoselectively reduced to the corresponding amines using recyclable ...
Removal of some commonly used protecting groups in peptide synthesis by catalytic transfer hydrogena...
Azo compounds are conveniently reduced to hydrazo compounds by using commercial zinc dust and hydraz...
The reduction of azo compounds with magnesium powder as catalyst in the presence of ammonium chlorid...
Various aldoximes and ketoximes were selectively reduced to the corresponding amines by catalytic tr...
Azo compounds are conveniently reduced to either partially reduced hydrazo compounds or completely r...
A variety of functionalized alkyl and aryl primary amines have been prepared from corresponding azid...
Aliphatic and aromatic nitro compounds are selectively and rapidly reduced to their corresponding am...