Imidazoles constitute an important class of heterocyclic compounds with extensive potential use, from pharmaceuticals to optoelectronics. However, synthetic methodologies capable of producing novel nonsymmetric imidazoles are still scarce. In a combined synthesis, photophysical and computational investigation, we show that ruthenium(II) catalysis enables C−H/N−H alkyne annulation of nonsymmetric imidazoles derived from naturally occuring β-lapachone and nor-β-lapachone. This method provides an efficient and versatile tool for synthesizing fluorescent compounds with a broad application range
A novel Ru-catalyzed oxidative double annulation of heteroarenes with symmetrical and unsymmetrical ...
Double ruthenium(II)-catalyzed alkyne annulations of quinones were accomplished. Thus, a strategy is...
A novel Ru-catalyzed oxidative double annulation of heteroarenes with symmetrical and unsymmetrical ...
Rhodium(III) catalysis enabled C–H/N–H alkyne annulation of nonsymmetric imidazole derivatives. This...
DoctorLight had the potential to serve as an inexpensive, abundant, renewable, and nonpolluting reag...
Alkynylated heteroarenes, and in particular alkynylazoles, represent a recurring structural motif fo...
π-Extension of 2-aryl-phenanthroimidazoles via rhodium(III)-catalyzed C–H activation and alkyne ann...
π-Extension of 2-aryl-phenanthroimidazoles via rhodium(III)-catalyzed C–H activation and alkyne ann...
π-Extension of 2-aryl-phenanthroimidazoles via rhodium(III)-catalyzed C–H activation and alkyne ann...
π-Extension of 2-aryl-phenanthroimidazoles via rhodium(III)-catalyzed C–H activation and alkyne ann...
Hydroxyl-assisted oxidative annulations of alkynes were accomplished with an inexpensive ruthenium(I...
New imidazolium and imidazolinium salts were synthesized and their ability to act as stable N-hetero...
In last few decades, the transition metal-catalyzed C-H bond activation and alkyne annulation reacti...
Synthesis of imidazo-fused polyheterocyclic molecular frameworks, viz. imidazo[1,2-a]pyrrolo[3,4-e]p...
Synthesis of imidazo-fused polyheterocyclic molecular frameworks, viz. imidazo[1,2-a]pyrrolo[3,4-e]p...
A novel Ru-catalyzed oxidative double annulation of heteroarenes with symmetrical and unsymmetrical ...
Double ruthenium(II)-catalyzed alkyne annulations of quinones were accomplished. Thus, a strategy is...
A novel Ru-catalyzed oxidative double annulation of heteroarenes with symmetrical and unsymmetrical ...
Rhodium(III) catalysis enabled C–H/N–H alkyne annulation of nonsymmetric imidazole derivatives. This...
DoctorLight had the potential to serve as an inexpensive, abundant, renewable, and nonpolluting reag...
Alkynylated heteroarenes, and in particular alkynylazoles, represent a recurring structural motif fo...
π-Extension of 2-aryl-phenanthroimidazoles via rhodium(III)-catalyzed C–H activation and alkyne ann...
π-Extension of 2-aryl-phenanthroimidazoles via rhodium(III)-catalyzed C–H activation and alkyne ann...
π-Extension of 2-aryl-phenanthroimidazoles via rhodium(III)-catalyzed C–H activation and alkyne ann...
π-Extension of 2-aryl-phenanthroimidazoles via rhodium(III)-catalyzed C–H activation and alkyne ann...
Hydroxyl-assisted oxidative annulations of alkynes were accomplished with an inexpensive ruthenium(I...
New imidazolium and imidazolinium salts were synthesized and their ability to act as stable N-hetero...
In last few decades, the transition metal-catalyzed C-H bond activation and alkyne annulation reacti...
Synthesis of imidazo-fused polyheterocyclic molecular frameworks, viz. imidazo[1,2-a]pyrrolo[3,4-e]p...
Synthesis of imidazo-fused polyheterocyclic molecular frameworks, viz. imidazo[1,2-a]pyrrolo[3,4-e]p...
A novel Ru-catalyzed oxidative double annulation of heteroarenes with symmetrical and unsymmetrical ...
Double ruthenium(II)-catalyzed alkyne annulations of quinones were accomplished. Thus, a strategy is...
A novel Ru-catalyzed oxidative double annulation of heteroarenes with symmetrical and unsymmetrical ...