The reaction of aromatic nitroso derivatives with enolizable carbonyl compounds (nitroso aldol reaction) to give either a-hydroxyamino or a-aminoxy carbonyl compounds is an important synthetic method. This review illustrates the recent advances in rendering the process regio- and enantioselective as well as catalytic. By employing metal and organic catalysts a range of a-amino (a-oxyamination) and a-hydroxy (a-aminoxylation) carbonyl derivatives can be generated with total regioselectivity and high levels of enantiomeric excess
The development of efficient methods for the formation of carbon-nitrogen bonds is of great interest...
Highly enantiomerically enriched 2-bromo-2-nitroalkan-1-ols are prepared by direct condensation of a...
The asymmetric conjugate addition of carbon and heteroatom nucleophiles to nitroalkenes is a very in...
The reaction of aromatic nitroso derivatives with enolizable carbonyl compounds (nitroso aldol react...
The power of nitrosocarbonyl chemistry and demonstrate their potential as new viable electrophilic s...
The aldol reaction plays an important role in organic synthesis and provides very useful synthetic t...
The aldol reaction plays an important role in organic synthesis and provides very useful synthetic t...
Recoverable (S)-BINAM-L-prolinamide in combination with benzoic acid catalyzes and accelerates the ...
The conjugate addition of nitroalkanes to electron-poor alkenes is a widely used process which only ...
C-H functionalisation reactions aim for the selective cleavage of C-H bonds, and formation of a new ...
peer reviewedC-Nitroso species are characterized by a unique nitrogen–oxygen combination located nex...
The chemical synthesis of organic molecules involves, at its very essence, the creation of carbon–ca...
The development of efficient methods for the formation of carbon-nitrogen bonds is of great interest...
The aldol reaction is one of the most important carbon–carbon bond formations in synthetic organic c...
The first example of a Cu-catalyzed asymmetric <i>O</i>-nitrosocarbonyl aldol reaction is described....
The development of efficient methods for the formation of carbon-nitrogen bonds is of great interest...
Highly enantiomerically enriched 2-bromo-2-nitroalkan-1-ols are prepared by direct condensation of a...
The asymmetric conjugate addition of carbon and heteroatom nucleophiles to nitroalkenes is a very in...
The reaction of aromatic nitroso derivatives with enolizable carbonyl compounds (nitroso aldol react...
The power of nitrosocarbonyl chemistry and demonstrate their potential as new viable electrophilic s...
The aldol reaction plays an important role in organic synthesis and provides very useful synthetic t...
The aldol reaction plays an important role in organic synthesis and provides very useful synthetic t...
Recoverable (S)-BINAM-L-prolinamide in combination with benzoic acid catalyzes and accelerates the ...
The conjugate addition of nitroalkanes to electron-poor alkenes is a widely used process which only ...
C-H functionalisation reactions aim for the selective cleavage of C-H bonds, and formation of a new ...
peer reviewedC-Nitroso species are characterized by a unique nitrogen–oxygen combination located nex...
The chemical synthesis of organic molecules involves, at its very essence, the creation of carbon–ca...
The development of efficient methods for the formation of carbon-nitrogen bonds is of great interest...
The aldol reaction is one of the most important carbon–carbon bond formations in synthetic organic c...
The first example of a Cu-catalyzed asymmetric <i>O</i>-nitrosocarbonyl aldol reaction is described....
The development of efficient methods for the formation of carbon-nitrogen bonds is of great interest...
Highly enantiomerically enriched 2-bromo-2-nitroalkan-1-ols are prepared by direct condensation of a...
The asymmetric conjugate addition of carbon and heteroatom nucleophiles to nitroalkenes is a very in...