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

Por um escritor misterioso
Last updated 13 janeiro 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
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
Rhodium(III)-Catalyzed Intermolecular Direct Amination of Aromatic
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
Iridium-Catalyzed C–H Amination with Anilines at Room
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
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
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
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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
Christoph Grohmann - Senior Scientist, II - Firefly Biologics
Rh[III]-Catalyzed C–H Amidation Using Aroyloxycarbamates To Give N-Boc  Protected Arylamines
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