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Rh[III]-Catalyzed C–H Amidation Using Aroyloxycarbamates To Give N-Boc Protected Arylamines

Por um escritor misterioso
Last updated 20 outubro 2024
Rh[III]-Catalyzed C–H Amidation Using Aroyloxycarbamates To Give N-Boc Protected Arylamines
Rh[III]-Catalyzed C–H Amidation Using Aroyloxycarbamates To Give N-Boc Protected Arylamines
Rh(III)- and Ir(III)-Catalyzed Direct C–H Bond Transformations to
Rh[III]-Catalyzed C–H Amidation Using Aroyloxycarbamates To Give N-Boc Protected Arylamines
N -Aroyloxycarbamates as switchable nitrogen and oxygen precursor
Rh[III]-Catalyzed C–H Amidation Using Aroyloxycarbamates To Give N-Boc Protected Arylamines
Dirhodium-catalyzed C-H arene amination using hydroxylamines
Rh[III]-Catalyzed C–H Amidation Using Aroyloxycarbamates To Give N-Boc Protected Arylamines
Directing group strategies in rhodium-catalyzed C–H amination
Rh[III]-Catalyzed C–H Amidation Using Aroyloxycarbamates To Give N-Boc Protected Arylamines
Mechanism of the Rhodium(III)-Catalyzed Arylation of Imines via C
Rh[III]-Catalyzed C–H Amidation Using Aroyloxycarbamates To Give N-Boc Protected Arylamines
Copper-Mediated Amination of Aryl C–H Bonds with the Direct Use of
Rh[III]-Catalyzed C–H Amidation Using Aroyloxycarbamates To Give N-Boc Protected Arylamines
N -Aroyloxycarbamates as switchable nitrogen and oxygen precursor
Rh[III]-Catalyzed C–H Amidation Using Aroyloxycarbamates To Give N-Boc Protected Arylamines
Table 4 from Iridium-catalyzed intermolecular amidation of sp³ C-H
Rh[III]-Catalyzed C–H Amidation Using Aroyloxycarbamates To Give N-Boc Protected Arylamines
N -Aroyloxycarbamates as switchable nitrogen and oxygen precursor
Rh[III]-Catalyzed C–H Amidation Using Aroyloxycarbamates To Give N-Boc Protected Arylamines
Frank GLORIUS, Prof. Dr., University of Münster, Münster
Rh[III]-Catalyzed C–H Amidation Using Aroyloxycarbamates To Give N-Boc Protected Arylamines
Rh(III)- and Ir(III)-Catalyzed Direct C–H Bond Transformations to
Rh[III]-Catalyzed C–H Amidation Using Aroyloxycarbamates To Give N-Boc Protected Arylamines
Rhodium‐Catalyzed C(sp2)‐ or C(sp3)−H Bond Functionalization
Rh[III]-Catalyzed C–H Amidation Using Aroyloxycarbamates To Give N-Boc Protected Arylamines
Directing group strategies in rhodium-catalyzed C–H amination
Rh[III]-Catalyzed C–H Amidation Using Aroyloxycarbamates To Give N-Boc Protected Arylamines
Selective Carbon‐Carbon Bond Amination with Redox‐Active Aminating
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