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

Por um escritor misterioso
Last updated 10 março 2025
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
Rhodium‐Catalyzed C(sp2)‐ or C(sp3)−H Bond Functionalization
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
N-Methoxyamide: An Alternative Amidation Reagent in the Rhodium
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
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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
Recent advances in transition-metal catalyzed nitrene transfer
Rh[III]-Catalyzed C–H Amidation Using Aroyloxycarbamates To Give N-Boc  Protected Arylamines
Rh(III)-Catalyzed C–H Amidation of Arenes with N-Methoxyamide as
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

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