The tetracyclic indoloindol-3-one core has been forged from easily accessible 2,2′-bis-bromochalcones employing a reaction cascade comprising Cu-catalyzed SNAr with azide; nitrene C–H insertion and intramolecular Ullmann reaction with all three C–N bond formations in one-go
Efficient synthetic routes to pyrazolo[3,4-b]indoles and pyrazolo[1,5-a]benzimidazoles via intramole...
A Cu(I)-catalyzed [3 + 2] intramolecular cycloaddition reaction of N-indole-tethered cyclopropenes ...
Polysubstituted indolizine derivatives are constructed via intramolecular C--N bond formation/C--H b...
The tetracyclic indoloindol-3-one core has been forged from easily accessible 2,2′-bis-bromochalcone...
A variety of functionalities, including the whole range of halogen substituents, are tolerated in th...
Multisubstituted indoles were synthesized via a one-pot tandem copper-catalyzed Ullmann-type C–N bon...
This perspective reports on some of the main copper-catalyzed routes to the construction of the pyrr...
3-Sulfonyl[1,2,3]triazolo[4,5-<i>b</i>]indoles were efficiently prepared via a tandem catalysis ...
A copper-catalyzed Friedel–Crafts propargylation/hydroamination/aromatization sequence is described....
A new synthetic approach for the synthesis of pyrrolo[3,2-b]indoles has been developed in two steps....
An annulation cascades of N-allyl-N-((2-bromoaryl)ethynyl)amides with terminal alkynes or 1,3-dica...
Symmetrical 3,3-diaryl-2-iminoindoles were prepared from 3-diazoindolin-2-imines and indoles via a c...
A palladium- and copper-catalyzed tandem N–H/C–H bond functionalization reaction of <i>ortho</i>-(2-...
3-Allyl-3-arylthioindolin-2-imines and 3-allenyl-3-arylthioindolin- 2-imines were synthesized via th...
Copper(II) trifluoromethanesulfonate (Cu(OTf)<sub>2</sub>) efficiently catalyzes the C–C coupling ...
Efficient synthetic routes to pyrazolo[3,4-b]indoles and pyrazolo[1,5-a]benzimidazoles via intramole...
A Cu(I)-catalyzed [3 + 2] intramolecular cycloaddition reaction of N-indole-tethered cyclopropenes ...
Polysubstituted indolizine derivatives are constructed via intramolecular C--N bond formation/C--H b...
The tetracyclic indoloindol-3-one core has been forged from easily accessible 2,2′-bis-bromochalcone...
A variety of functionalities, including the whole range of halogen substituents, are tolerated in th...
Multisubstituted indoles were synthesized via a one-pot tandem copper-catalyzed Ullmann-type C–N bon...
This perspective reports on some of the main copper-catalyzed routes to the construction of the pyrr...
3-Sulfonyl[1,2,3]triazolo[4,5-<i>b</i>]indoles were efficiently prepared via a tandem catalysis ...
A copper-catalyzed Friedel–Crafts propargylation/hydroamination/aromatization sequence is described....
A new synthetic approach for the synthesis of pyrrolo[3,2-b]indoles has been developed in two steps....
An annulation cascades of N-allyl-N-((2-bromoaryl)ethynyl)amides with terminal alkynes or 1,3-dica...
Symmetrical 3,3-diaryl-2-iminoindoles were prepared from 3-diazoindolin-2-imines and indoles via a c...
A palladium- and copper-catalyzed tandem N–H/C–H bond functionalization reaction of <i>ortho</i>-(2-...
3-Allyl-3-arylthioindolin-2-imines and 3-allenyl-3-arylthioindolin- 2-imines were synthesized via th...
Copper(II) trifluoromethanesulfonate (Cu(OTf)<sub>2</sub>) efficiently catalyzes the C–C coupling ...
Efficient synthetic routes to pyrazolo[3,4-b]indoles and pyrazolo[1,5-a]benzimidazoles via intramole...
A Cu(I)-catalyzed [3 + 2] intramolecular cycloaddition reaction of N-indole-tethered cyclopropenes ...
Polysubstituted indolizine derivatives are constructed via intramolecular C--N bond formation/C--H b...
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