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

Por um escritor misterioso

Descrição

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
Directing group strategies in rhodium-catalyzed C–H amination
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
Rhodium(III)-Catalyzed Intermolecular Amidation with Azides via C
Rh[III]-Catalyzed C–H Amidation Using Aroyloxycarbamates To Give N-Boc  Protected Arylamines
Ortho vs ipso: site-selective Pd and norbornene-catalyzed arene
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
Iridium-catalyzed intermolecular amidation of sp³ C-H bonds: late
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
Tunable Arylative Cyclization of 1,6-Enynes Triggered by Rhodium
de por adulto (o preço varia de acordo com o tamanho do grupo)