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Experimental and computational studies on H <sub>2</sub> O-promoted, Rh-catalyzed transient-ligand-free <i>ortho</i> -C(sp <sup>2</sup> )–H amidation of benzaldehydes with dioxazolones

https://doi.org/10.1039/c8cc04904a
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Metal-Controlled, Regioselective, Direct Intermolecular α- or γ-Amination with Azodicarboxylates
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Comparative Catalytic Activity of Group 9 [Cp*M<sup>III</sup>] Complexes: Cobalt‐Catalyzed CH Amidation of Arenes with Dioxazolones as Amidating Reagents
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Oxazolinyl-Assisted C–H Amidation by Cobalt(III) Catalysis
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Mechanochemical Rhodium(III)-Catalyzed C–H Bond Amidation of Arenes with Dioxazolones under Solventless Conditions in a Ball Mill
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Thioamide‐Directed Cobalt(III)‐Catalyzed Selective Amidation of C(sp<sup>3</sup>)−H Bonds
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Selective formation of γ-lactams via C–H amidation enabled by tailored iridium catalysts
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Rh‐Catalyzed Annulation of <i>ortho</i>‐C−H Bonds of 2‐Arylimidazoles with 1,4,2‐Dioxazol‐5‐ones toward 5‐Arylimidazo[1,2‐<i>c</i>]quinazolines
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Synthesis of Indene Frameworks via Rhodium-Catalyzed Cascade Cyclization of Aromatic Ketone and Unsaturated Carbonyl Compounds
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Rhodium(III)‐Catalyzed [3+2] Annulation of 5‐Aryl‐2,3‐dihydro‐1<i>H</i>‐pyrroles with Internal Alkynes through C(sp<sup>2</sup>)H/Alkene Functionalization
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Rhodium(III)‐Catalyzed [3+2]/[5+2] Annulation of 4‐Aryl 1,2,3‐Triazoles with Internal Alkynes through Dual C(sp<sup>2</sup>)H Functionalization
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Rhodium(III)-Catalyzed Direct Cyanation of Aromatic C–H Bond to Form 2-(Alkylamino)benzonitriles Using <i>N</i>-Nitroso As Directing Group
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Mechanistic Studies on the Rh(III)-Mediated Amido Transfer Process Leading to Robust C–H Amination with a New Type of Amidating Reagent
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Iterative C−H Functionalization Leading to Multiple Amidations of Anilides
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Rh‐catalyzed Transient Directing Group Promoted C—H Amidation of Benzaldehydes Utilizing Dioxazolones
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A Convenient Allenoate-Based Synthesis of 2-Quinolin-2-yl Malonates and β-Ketoesters
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Asymmetric Iron‐Catalyzed C−H Alkylation Enabled by Remote Ligand <i>meta</i>‐Substitution
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PPh<sub>3</sub>O as an Activating Reagent for One-Pot Stereoselective Syntheses of Di- and Polybrominated Esters from Simple Aldehydes
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