A simple and efficient protocol for the regioselective synthesis of 5-aminooxazoles is disclosed. The reaction, catalyzed by a cheap Cp*Co(III) catalyst, starts from easily accessible <i>N</i>-(pivaloyloxy)amides and ynamides. Mild reaction conditions, a broad substrate scope, good functional group tolerance, and good to excellent yields were observed
Oxadiazolones are first employed as the three-atom coupling partners in the Tf2NH-catalyzed cycloadd...
An efficient highly regioselective protocol for the synthesis of isomeric 1,3-diaryl (or 1-aryl-3-al...
A rhodium-catalyzed azide–alkyne cycloaddition of internal ynamides is described. The reaction could...
An unprecedented Tf2NH-catalyzed formal [3 + 2] cycloaddition of ynamides with dioxazoles was develo...
A novel and straightforward protocol is demonstrated for the synthesis of highly substituted oxazole...
International audienceAn original cobalt-catalyzed ynamide carbozincation leading mainly to diverse ...
International audienceAn original cobalt-catalyzed ynamide carbozincation leading mainly to diverse ...
A novel and straightforward protocol is demonstrated for the synthesis of highly substituted oxazole...
International audienceAn original cobalt-catalyzed ynamide carbozincation leading mainly to diverse ...
International audienceAn original cobalt-catalyzed ynamide carbozincation leading mainly to diverse ...
International audienceAn original cobalt-catalyzed ynamide carbozincation leading mainly to diverse ...
International audienceAn original cobalt-catalyzed ynamide carbozincation leading mainly to diverse ...
International audienceAn original cobalt-catalyzed ynamide carbozincation leading mainly to diverse ...
International audienceAn original cobalt-catalyzed ynamide carbozincation leading mainly to diverse ...
An efficient cobalt-catalyzed C–H amidation of 7-azaindoles was developed by using dioxazolones as t...
Oxadiazolones are first employed as the three-atom coupling partners in the Tf2NH-catalyzed cycloadd...
An efficient highly regioselective protocol for the synthesis of isomeric 1,3-diaryl (or 1-aryl-3-al...
A rhodium-catalyzed azide–alkyne cycloaddition of internal ynamides is described. The reaction could...
An unprecedented Tf2NH-catalyzed formal [3 + 2] cycloaddition of ynamides with dioxazoles was develo...
A novel and straightforward protocol is demonstrated for the synthesis of highly substituted oxazole...
International audienceAn original cobalt-catalyzed ynamide carbozincation leading mainly to diverse ...
International audienceAn original cobalt-catalyzed ynamide carbozincation leading mainly to diverse ...
A novel and straightforward protocol is demonstrated for the synthesis of highly substituted oxazole...
International audienceAn original cobalt-catalyzed ynamide carbozincation leading mainly to diverse ...
International audienceAn original cobalt-catalyzed ynamide carbozincation leading mainly to diverse ...
International audienceAn original cobalt-catalyzed ynamide carbozincation leading mainly to diverse ...
International audienceAn original cobalt-catalyzed ynamide carbozincation leading mainly to diverse ...
International audienceAn original cobalt-catalyzed ynamide carbozincation leading mainly to diverse ...
International audienceAn original cobalt-catalyzed ynamide carbozincation leading mainly to diverse ...
An efficient cobalt-catalyzed C–H amidation of 7-azaindoles was developed by using dioxazolones as t...
Oxadiazolones are first employed as the three-atom coupling partners in the Tf2NH-catalyzed cycloadd...
An efficient highly regioselective protocol for the synthesis of isomeric 1,3-diaryl (or 1-aryl-3-al...
A rhodium-catalyzed azide–alkyne cycloaddition of internal ynamides is described. The reaction could...