Ferric nitrate with catalytic TEMPO has been identified as a useful reagent for regio- and stereoselective nitration of a wide variety of aromatic, aliphatic, and heteroaromatic olefins. This reaction provided nitroolefins in preparatively useful yields with excellent E-selectivity. Due to its mild nature and operational simplicity, the present protocol is expected to find application in synthetic setup
Nitroaromatic compounds represent one of the essential classes of molecules that are widely used as ...
Aromatic hydrocarbons are nitrated by metallic nitrates impregnated on the K10 montmorillonite in th...
A regioselective nitration of BN-substituted arene compounds has been successfully developed. The fi...
Nitroolefins are essential elements for both synthetic chemistry and medicinal research. Despite sig...
Nitroolefins are essential elements for both synthetic chemistry and medicinal research. Despite sig...
Nitroolefin is a common and versatile reagent. Its synthesis from olefin is generally limited by the...
Nitroolefins are usually synthesized using the Henry reaction. Here we report an alternative metal-f...
The use of N2O5 and a Fe(III) catalyst for the nitration of aromatic rings is described. This method...
Nitroolefins are important synthetic intermediates in the field of organic synthesis as well as in m...
Acid catalyzed nitration has been examined using a variety of novel nitration agents: guanidine nitr...
Nitration of aromatic Compounds is triggered by Vilsmeier-Haack reagent (DMF/POCl3) or (DMF/SOCl2) i...
Novel nitration systems comprising nitric acid, trifluoroacetic anhydride and zeolite Hβ, with or wi...
Abstract: Iron phthalocyanine with iron sulfate has been successfully applied for high chemo- and ...
High para-selectivity (upto 92%) and isolated yield (90%) are achieved in the nitration of chloroben...
Highly regiospecific mononitration of phenols and substituted phenols is accomplished employing a me...
Nitroaromatic compounds represent one of the essential classes of molecules that are widely used as ...
Aromatic hydrocarbons are nitrated by metallic nitrates impregnated on the K10 montmorillonite in th...
A regioselective nitration of BN-substituted arene compounds has been successfully developed. The fi...
Nitroolefins are essential elements for both synthetic chemistry and medicinal research. Despite sig...
Nitroolefins are essential elements for both synthetic chemistry and medicinal research. Despite sig...
Nitroolefin is a common and versatile reagent. Its synthesis from olefin is generally limited by the...
Nitroolefins are usually synthesized using the Henry reaction. Here we report an alternative metal-f...
The use of N2O5 and a Fe(III) catalyst for the nitration of aromatic rings is described. This method...
Nitroolefins are important synthetic intermediates in the field of organic synthesis as well as in m...
Acid catalyzed nitration has been examined using a variety of novel nitration agents: guanidine nitr...
Nitration of aromatic Compounds is triggered by Vilsmeier-Haack reagent (DMF/POCl3) or (DMF/SOCl2) i...
Novel nitration systems comprising nitric acid, trifluoroacetic anhydride and zeolite Hβ, with or wi...
Abstract: Iron phthalocyanine with iron sulfate has been successfully applied for high chemo- and ...
High para-selectivity (upto 92%) and isolated yield (90%) are achieved in the nitration of chloroben...
Highly regiospecific mononitration of phenols and substituted phenols is accomplished employing a me...
Nitroaromatic compounds represent one of the essential classes of molecules that are widely used as ...
Aromatic hydrocarbons are nitrated by metallic nitrates impregnated on the K10 montmorillonite in th...
A regioselective nitration of BN-substituted arene compounds has been successfully developed. The fi...