International audienceThe electrophilicity of 4 different 3-nitroindole derivatives has been evaluated by Mayr’s linear free energy relationship (log k(20 °C) = sN(E + N)) and reveals unexpected values for aromatic compounds, in the nitrostyrene range. 3-Nitroindoles are sufficiently electrophilic to interact with a common diene namely the Danishefsky's diene at room temperature, in the absence of any activator, to furnish smoothly the dearomatized (4+2) cycloadducts in good yields
International audienceDearomatization of conventional nitroarenes by lithiated enolates derived from...
International audienceThe indol(in)e building block is one of the "privileged-structures" for the ph...
The chemo-, regio-, and stereoselectivities of multicomponent [4 + 2]/[3 + 2] domino cycloaddition r...
International audienceThe electrophilicity of 4 different 3-nitroindole derivatives has been evaluat...
International audienceThe electrophilicity of 4 different 3-nitroindole derivatives has been evaluat...
International audienceThe electrophilicity of 4 different 3-nitroindole derivatives has been evaluat...
3-Nitroindoles (10) are prepared in good yields via a thermal 6 pi-electrocyclization of 2,3-(dialke...
International audienceThrough the linear free energy relationship log k=sN (N + E), the electrophili...
International audienceThrough the linear free energy relationship log k=sN (N + E), the electrophili...
The global electrophilicity power, ω, of a series of dipoles and dipolarophiles commonly used in 1,3...
International audienceThe chemo-, regio-, and stereoselectivities of multicomponent [4 + 2]/[3 + 2] ...
International audienceThe chemo-, regio-, and stereoselectivities of multicomponent [4 + 2]/[3 + 2] ...
International audienceThe chemo-, regio-, and stereoselectivities of multicomponent [4 + 2]/[3 + 2] ...
The Diels-Alder reaction is considered a pericyclic procces. However, depending of the structure of ...
International audienceDearomatization of conventional nitroarenes by lithiated enolates derived from...
International audienceDearomatization of conventional nitroarenes by lithiated enolates derived from...
International audienceThe indol(in)e building block is one of the "privileged-structures" for the ph...
The chemo-, regio-, and stereoselectivities of multicomponent [4 + 2]/[3 + 2] domino cycloaddition r...
International audienceThe electrophilicity of 4 different 3-nitroindole derivatives has been evaluat...
International audienceThe electrophilicity of 4 different 3-nitroindole derivatives has been evaluat...
International audienceThe electrophilicity of 4 different 3-nitroindole derivatives has been evaluat...
3-Nitroindoles (10) are prepared in good yields via a thermal 6 pi-electrocyclization of 2,3-(dialke...
International audienceThrough the linear free energy relationship log k=sN (N + E), the electrophili...
International audienceThrough the linear free energy relationship log k=sN (N + E), the electrophili...
The global electrophilicity power, ω, of a series of dipoles and dipolarophiles commonly used in 1,3...
International audienceThe chemo-, regio-, and stereoselectivities of multicomponent [4 + 2]/[3 + 2] ...
International audienceThe chemo-, regio-, and stereoselectivities of multicomponent [4 + 2]/[3 + 2] ...
International audienceThe chemo-, regio-, and stereoselectivities of multicomponent [4 + 2]/[3 + 2] ...
The Diels-Alder reaction is considered a pericyclic procces. However, depending of the structure of ...
International audienceDearomatization of conventional nitroarenes by lithiated enolates derived from...
International audienceDearomatization of conventional nitroarenes by lithiated enolates derived from...
International audienceThe indol(in)e building block is one of the "privileged-structures" for the ph...
The chemo-, regio-, and stereoselectivities of multicomponent [4 + 2]/[3 + 2] domino cycloaddition r...