Nitroolefins are essential elements for both synthetic chemistry and medicinal research. Despite significant improvements in nitration of olefin an efficient metal-free synthesis remains elusive so far. Herein, we disclose a new set of reagents to access nitroolefins in a single step under metal-free conditions. A wide range of olefins with diverse functionalities has been nitrated in synthetically useful yields. This transformation is operationally simple and exhibits excellent E-selectivity. Furthermore, site selective nitration in a complex setup makes this method advantageous
Nitroaromatics and nitroheteroaromatics serve as key building blocks and intermediates in synthesis,...
A novel, mild and convenient method for the nitrodecarboxylation of substituted cinnamic acid deriva...
Nitration of relatively electron-rich arenes does not require an additive or a solvent. For example,...
Nitroolefins are essential elements for both synthetic chemistry and medicinal research. Despite sig...
Ferric nitrate with catalytic TEMPO has been identified as a useful reagent for regio- and stereosel...
Nitroolefins are important synthetic intermediates in the field of organic synthesis as well as in m...
Nitroolefins are usually synthesized using the Henry reaction. Here we report an alternative metal-f...
Nitroolefin is a common and versatile reagent. Its synthesis from olefin is generally limited by the...
An efficient copper nitrate mediated chloronitration reaction was developed for the direct synthesis...
An efficient, mild, and metal-free arylation of nitroalkanes with diaryliodonium salts has been deve...
Nitroaromatic compounds represent one of the essential classes of molecules that are widely used as ...
A convenient, inexpensive and efficient 'one-pot' process is described for the selective nitration o...
Nitroaromatic compounds represent one of the essential classes of molecules that are widely used as ...
Novel nitration systems comprising nitric acid, trifluoroacetic anhydride and zeolite Hβ, with or wi...
An efficient, mild, and metal-free arylation of nitro-alkanes with diaryliodonium salts has been dev...
Nitroaromatics and nitroheteroaromatics serve as key building blocks and intermediates in synthesis,...
A novel, mild and convenient method for the nitrodecarboxylation of substituted cinnamic acid deriva...
Nitration of relatively electron-rich arenes does not require an additive or a solvent. For example,...
Nitroolefins are essential elements for both synthetic chemistry and medicinal research. Despite sig...
Ferric nitrate with catalytic TEMPO has been identified as a useful reagent for regio- and stereosel...
Nitroolefins are important synthetic intermediates in the field of organic synthesis as well as in m...
Nitroolefins are usually synthesized using the Henry reaction. Here we report an alternative metal-f...
Nitroolefin is a common and versatile reagent. Its synthesis from olefin is generally limited by the...
An efficient copper nitrate mediated chloronitration reaction was developed for the direct synthesis...
An efficient, mild, and metal-free arylation of nitroalkanes with diaryliodonium salts has been deve...
Nitroaromatic compounds represent one of the essential classes of molecules that are widely used as ...
A convenient, inexpensive and efficient 'one-pot' process is described for the selective nitration o...
Nitroaromatic compounds represent one of the essential classes of molecules that are widely used as ...
Novel nitration systems comprising nitric acid, trifluoroacetic anhydride and zeolite Hβ, with or wi...
An efficient, mild, and metal-free arylation of nitro-alkanes with diaryliodonium salts has been dev...
Nitroaromatics and nitroheteroaromatics serve as key building blocks and intermediates in synthesis,...
A novel, mild and convenient method for the nitrodecarboxylation of substituted cinnamic acid deriva...
Nitration of relatively electron-rich arenes does not require an additive or a solvent. For example,...