Casascp 6669

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

Por um escritor misterioso
Last updated 06 abril 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
Directing‐Group‐Assisted Transition‐Metal‐Catalyzed Direct
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
Directing group strategies in rhodium-catalyzed C–H amination
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
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
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
Directing group strategies in rhodium-catalyzed C–H amination
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
Microwave-assisted protection of primary amines as 2,5
Rh[III]-Catalyzed C–H Amidation Using Aroyloxycarbamates To Give N-Boc Protected Arylamines
A Facile Access to Primary Alkylamines and Anilines via Ir(III
Rh[III]-Catalyzed C–H Amidation Using Aroyloxycarbamates To Give N-Boc Protected Arylamines
Rh( iii )-Catalysed cascade C–H imidization/cyclization of N
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