Difficult-to-access alkyl-substituted quinolines are formed directly from commercially available anilines, aldehydes, and alkynes bearing a variety of substituents. Copper(II) triflate catalyzes this three-component coupling without ligand, cocatalyst, solvent, or inert atmosphere. In addition, a two-component Povarov reaction forms 2,3-dialkyl quinolines under the same green conditions that enable the selective three-component synthesis of 2-alkyl quinolines as well as more common aryl quinolines
International audienceA convenient one-pot synthesis of 2,3-di- ACHTUNGTRENUNGsubstituted, 2,3,6-tri...
A sequential catalytic process has been developed based on gold-catalyzed nucleophilic addition of t...
Tetrahydroquinoline skeletons can be formed by a CuCl2-catalyzed one-potreaction of N-methyl-N-alkyl...
A variety of unique small molecule families were created through copper-catalyzed three-component co...
A variety of unique small molecule families were created through copper-catalyzed three-component co...
An efficient cascade copper-catalyzed intermolecular Ullmann-type C–N coupling/enamine condensation ...
A rapid microwave-assisted, catalyst-free, three-component synthesis of various 2-anilinoquinolines ...
Microwave-assisted one-pot three-component reaction between aromatic amines, aromatic aldehydes and ...
Generation of trifluoromethyl-substituted pyrrolo[3,2-<i>c</i>]quinolines via a copper(II)-cataly...
Generation of trifluoromethyl-substituted pyrrolo[3,2-<i>c</i>]quinolines via a copper(II)-cataly...
An efficient method for the direct synthesis of substituted quinolines from anilines and aldehydes t...
A synthetic approach to quinindoline derivatives by the Cu-catalyzed dual cyclization has been devel...
We describe here our results from the copper-catalyzed three component reaction of 2-azidobenzaldehy...
International audienceA convenient one-pot synthesis of 2,3-di- ACHTUNGTRENUNGsubstituted, 2,3,6-tri...
International audienceA convenient one-pot synthesis of 2,3-di- ACHTUNGTRENUNGsubstituted, 2,3,6-tri...
International audienceA convenient one-pot synthesis of 2,3-di- ACHTUNGTRENUNGsubstituted, 2,3,6-tri...
A sequential catalytic process has been developed based on gold-catalyzed nucleophilic addition of t...
Tetrahydroquinoline skeletons can be formed by a CuCl2-catalyzed one-potreaction of N-methyl-N-alkyl...
A variety of unique small molecule families were created through copper-catalyzed three-component co...
A variety of unique small molecule families were created through copper-catalyzed three-component co...
An efficient cascade copper-catalyzed intermolecular Ullmann-type C–N coupling/enamine condensation ...
A rapid microwave-assisted, catalyst-free, three-component synthesis of various 2-anilinoquinolines ...
Microwave-assisted one-pot three-component reaction between aromatic amines, aromatic aldehydes and ...
Generation of trifluoromethyl-substituted pyrrolo[3,2-<i>c</i>]quinolines via a copper(II)-cataly...
Generation of trifluoromethyl-substituted pyrrolo[3,2-<i>c</i>]quinolines via a copper(II)-cataly...
An efficient method for the direct synthesis of substituted quinolines from anilines and aldehydes t...
A synthetic approach to quinindoline derivatives by the Cu-catalyzed dual cyclization has been devel...
We describe here our results from the copper-catalyzed three component reaction of 2-azidobenzaldehy...
International audienceA convenient one-pot synthesis of 2,3-di- ACHTUNGTRENUNGsubstituted, 2,3,6-tri...
International audienceA convenient one-pot synthesis of 2,3-di- ACHTUNGTRENUNGsubstituted, 2,3,6-tri...
International audienceA convenient one-pot synthesis of 2,3-di- ACHTUNGTRENUNGsubstituted, 2,3,6-tri...
A sequential catalytic process has been developed based on gold-catalyzed nucleophilic addition of t...
Tetrahydroquinoline skeletons can be formed by a CuCl2-catalyzed one-potreaction of N-methyl-N-alkyl...