We disclose a unprecedented riboflavin promoted Nef reaction of primary nitroalkanes coupled with a nitroaldol reaction. This tandem process allows the synthesis of functionalized nitro alcohols under mild reaction conditions. Secondary nitroalkanes fail to give the expected nitroaldol products although they are consumed under the reaction conditions
The article describes the amination of different monobromoor monochloroflavones with primary and sec...
An efficient and practical one-pot protocol for the reduction of b-nitro alcohols to their correspon...
In this short note, we report the synthesis of 6-methyl-2-nitro-1-phenyl-hept-4-en-3-ol by a LiAlH4 ...
We disclose a unprecedented riboflavin promoted Nef reaction of primary nitroalkanes coupled with a ...
Nitro alkanes are valuable starting materials for functionalisation via their corresponding anions a...
The high reactivity and electron-withdrawing ability of the nitro group makes it a powerful tool in ...
Discover a comprehensive exploration of recent progress in the preparation of nitroalkanes from two ...
Nitroolefins are important synthetic intermediates in the field of organic synthesis as well as in m...
International audienceThe present brief account relates our discovery of new reactions revolving aro...
Nef reaction is one of the most commonly used method for the conversion of nitroalkanes to carbnyl c...
A variety of alpha,beta-unsaturated ketones can be easily converted, at room temperature, into beta...
Aliphatic nitro derivatives represent an important class of useful molecules in organic synthesis. ...
A highly selective C–H functionalization of nitrobenzenes and nitropyridines is reported using tande...
The article describes the amination of different monobromoor monochloroflavones with primary and sec...
An efficient and practical one-pot protocol for the reduction of b-nitro alcohols to their correspon...
In this short note, we report the synthesis of 6-methyl-2-nitro-1-phenyl-hept-4-en-3-ol by a LiAlH4 ...
We disclose a unprecedented riboflavin promoted Nef reaction of primary nitroalkanes coupled with a ...
Nitro alkanes are valuable starting materials for functionalisation via their corresponding anions a...
The high reactivity and electron-withdrawing ability of the nitro group makes it a powerful tool in ...
Discover a comprehensive exploration of recent progress in the preparation of nitroalkanes from two ...
Nitroolefins are important synthetic intermediates in the field of organic synthesis as well as in m...
International audienceThe present brief account relates our discovery of new reactions revolving aro...
Nef reaction is one of the most commonly used method for the conversion of nitroalkanes to carbnyl c...
A variety of alpha,beta-unsaturated ketones can be easily converted, at room temperature, into beta...
Aliphatic nitro derivatives represent an important class of useful molecules in organic synthesis. ...
A highly selective C–H functionalization of nitrobenzenes and nitropyridines is reported using tande...
The article describes the amination of different monobromoor monochloroflavones with primary and sec...
An efficient and practical one-pot protocol for the reduction of b-nitro alcohols to their correspon...
In this short note, we report the synthesis of 6-methyl-2-nitro-1-phenyl-hept-4-en-3-ol by a LiAlH4 ...