Copper‐Catalyzed Highly Regioselective Oxidative CH Bond Amidation of 2‐Arylpyridine Derivatives and 1‐Methylindoles
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- Type
- article
- Published
- 2010-03-08
- Cited by
- 150
- References
- 31
- OpenAlex
- https://openalex.org/W2035607313
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:95562380
Keywords
Chemistry, Regioselectivity, Catalysis, Halide, Bromide
References
- Ru-, Rh-, and Pd-catalyzed C-C bond formation involving C-H activation and addition on unsaturated substrates: reactions and mechanistic aspects.
- Cu(II)-catalyzed functionalizations of aryl C-H bonds using O2 as an oxidant.
- Cu(II)-catalyzed direct and site-selective arylation of indoles under mild conditions.
- Recent advances in aryl-aryl bond formation by direct arylation.
- Cross-dehydrogenative coupling (CDC): exploring C-C bond formations beyond functional group transformations.
- Combined C-H functionalization/C-N bond formation route to carbazoles.
- Oxidative Pd(II)-catalyzed C-H bond amination to carbazole at ambient temperature.
- Palladium-catalyzed methylation of aryl C-H bond by using peroxides.
- Copper-catalyzed coupling of alkylamines and aryl iodides: an efficient system even in an air atmosphere.
- Intermolecular amidation of unactivated sp2 and sp2 C-H bonds via palladium-catalyzed cascade C-H activation/nitrene insertion.
- Übergangsmetall‐katalysierte Kupplungsreaktionen unter C‐H‐Aktivierung
- Catalytic C-C, C-N, and C-O Ullmann-type coupling reactions.
- De novo design of biomimetic antimicrobial polymers
- Moderne Synthesemethoden: Kupfer-vermittelte C(Aryl)-O-, C(Aryl)-N- und C(Aryl)-S-Verknüpfungen
- Copper-mediated coupling reactions and their applications in natural products and designed biomolecules synthesis.
- Direct amination of azoles via catalytic C-H, N-H coupling.
- Transition-Metal-CatalyzedCarbon-Carbon Bond Formation via Carbon-HydrogenBond Cleavage
- Synthesis of beta-, gamma-, and delta-lactams via Pd(II)-catalyzed C-H activation reactions.
- A Palladium-Catalyzed Method for the Synthesis of Carbazoles via Tandem C-H Functionalization and C-N Bond Formation
- Aryl-aryl bond formation by transition-metal-catalyzed direct arylation.
Cited by
- Direct C-N coupling of imidazoles and benzylic compounds via iron-catalyzed oxidative activation of C-H bonds.
- Copper-catalyzed efficient direct amidation of 2-methylquinolines with amines.
- Cu(II)-Mediated C(sp(2))-H Hydroxylation.
- Synthesis of indolines by copper-mediated intramolecular aromatic C-h amination.
- Transition Metal-Catalyzed CH Activation of Indoles
- Reusable ionic liquid-catalyzed oxidative coupling of azoles and benzylic compounds via sp(3) C-N bond formation under metal-free conditions.
- Copper(I)‐Catalyzed Dehydrogenative Amidation of Arenes Using Air as the Oxidant
- Copper-catalyzed C(sp2)-H amidation with azides as amino sources.
- Regioselective C–H Bond Amination by Aminoiodanes
- Copper-catalyzed oxidative esterification of aldehydes with dialkyl peroxides: efficient synthesis of esters of tertiary alcohols
- 2-Trifluoroacetyl aminoindoles as useful intermediates for the preparation of 2-acylamino indoles
- 4-Aryl-2-quinolones from 3,3-diarylacrylamides through intramolecular copper-catalyzed C-H functionalization/C-N bond formation.
- Ruthenium porphyrin catalyzed diimination of indoles with aryl azides as the nitrene source.
- Iridium(III)-catalyzed direct C-7 amination of indolines with organic azides.
- Highly regioselective C-N bond formation through C-H azolation of indoles promoted by iodine in aqueous media.
- Copper-catalyzed direct amination of electron-deficient arenes with hydroxylamines.
- I2/TBHP-catalyzed chemoselective amination of indoles.
- Ruthenium‐katalysierte gekreuzte dehydrierende ortho‐N‐Carbazolierung von Diarylaminen: ein vielseitiger Zugang zu unsymmetrischen Diaminen
- Metal-free synthesis of allylic amines by cross-dehydrogenative-coupling of 1,3-diarylpropenes with anilines and amides under mild conditions.
- Copper-catalyzed intermolecular dehydrogenative amidation/amination of quinoline N-oxides with lactams/cyclamines.
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