All nitroso ene reactions so far reported follow exclusively stepwise reaction paths. Herein, we report the first concerted nitroso ene reaction that occurs between o-isotoluene (or its naphthalenic analogues) and nitroso compounds (e.g., nitrosomethane and 4-nitronitrosobenzene)
Pure nitric oxide does not add to alkenes containing acceptor or donor substituents, or to conjugate...
Nitration of 2,6-dimethyl-4-nitrophenol (40a) with fuming nitric acid gives the pair of C2-epimeric ...
The first catalytic method to directly introduce nitrone functionality onto aldehyde substrates is d...
International audienceThe present brief account relates our discovery of new reactions revolving aro...
Nitrosocarbonyl intermediates, generated at r.t. by the mild oxidation of nitrile oxides, undergo cl...
This thesis concerns the generation of geminally functionalised nitroso compounds and their subseque...
The development of efficient methods for the formation of carbon-nitrogen bonds is of great interest...
The authors present evidence that the shock-initiation chemistry of nitroarenes is dominated by the ...
International audienceA new cascade reaction to access C-pyrrolyl nitrones en route to isoxazolidine...
Nitrosoarenes react with nitrogen monoxide (nitric oxide) at room temperature and in aprotic media t...
Contrary to current belief, nitroethylene is a stable reagent and holds promise as a useful and reac...
Nitrosoarenes react with nitrogen monoxide (nitric oxide) at room temperature and in aprotic media t...
The reactivity of nitrosoalkenes toward dipyrromethanes, pyrrole, and 2,5-dimethylpyrrole is describ...
Nitrosocarbonyls are fleeting and highly reactive intermediates that undergo ene reactions in a two-...
Nitrosocarbonyl intermediates undergo ene reactions with allylic alcohols, affording regioisomeric a...
Pure nitric oxide does not add to alkenes containing acceptor or donor substituents, or to conjugate...
Nitration of 2,6-dimethyl-4-nitrophenol (40a) with fuming nitric acid gives the pair of C2-epimeric ...
The first catalytic method to directly introduce nitrone functionality onto aldehyde substrates is d...
International audienceThe present brief account relates our discovery of new reactions revolving aro...
Nitrosocarbonyl intermediates, generated at r.t. by the mild oxidation of nitrile oxides, undergo cl...
This thesis concerns the generation of geminally functionalised nitroso compounds and their subseque...
The development of efficient methods for the formation of carbon-nitrogen bonds is of great interest...
The authors present evidence that the shock-initiation chemistry of nitroarenes is dominated by the ...
International audienceA new cascade reaction to access C-pyrrolyl nitrones en route to isoxazolidine...
Nitrosoarenes react with nitrogen monoxide (nitric oxide) at room temperature and in aprotic media t...
Contrary to current belief, nitroethylene is a stable reagent and holds promise as a useful and reac...
Nitrosoarenes react with nitrogen monoxide (nitric oxide) at room temperature and in aprotic media t...
The reactivity of nitrosoalkenes toward dipyrromethanes, pyrrole, and 2,5-dimethylpyrrole is describ...
Nitrosocarbonyls are fleeting and highly reactive intermediates that undergo ene reactions in a two-...
Nitrosocarbonyl intermediates undergo ene reactions with allylic alcohols, affording regioisomeric a...
Pure nitric oxide does not add to alkenes containing acceptor or donor substituents, or to conjugate...
Nitration of 2,6-dimethyl-4-nitrophenol (40a) with fuming nitric acid gives the pair of C2-epimeric ...
The first catalytic method to directly introduce nitrone functionality onto aldehyde substrates is d...
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