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

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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
Rh(III)-Catalyzed C–H Amidation with N-Hydroxycarbamates: A New
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
Cu-Catalyzed Direct Amidation of Aromatic C–H Bonds: An Access to
Rh[III]-Catalyzed C–H Amidation Using Aroyloxycarbamates To Give N-Boc Protected Arylamines
Selective Carbon‐Carbon Bond Amination with Redox‐Active Aminating
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
Cobalt(II)-Catalyzed C–H and N–H Functionalization of 1
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
NHC)Cu-Catalyzed Mild C–H Amidation of (Hetero)arenes with
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