Rh[III]-Catalyzed C–H Amidation Using Aroyloxycarbamates To Give N-Boc Protected Arylamines
Por um escritor misterioso
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![Rh[III]-Catalyzed C–H Amidation Using Aroyloxycarbamates To Give N-Boc Protected Arylamines](https://pubs.acs.org/cms/10.1021/jacs.8b08826/asset/images/medium/ja-2018-08826w_0008.gif)
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](https://pubs.rsc.org/image/article/2022/OB/d2ob01157c/d2ob01157c-s12_hi-res.gif)
Directing group strategies in rhodium-catalyzed C–H amination
![Rh[III]-Catalyzed C–H Amidation Using Aroyloxycarbamates To Give N-Boc Protected Arylamines](https://ars.els-cdn.com/content/image/1-s2.0-S1001841723006113-sc4.jpg)
Recent advances in transition-metal catalyzed nitrene transfer
Rhodium(III)-Catalyzed Intermolecular Amidation with Azides via C
![Rh[III]-Catalyzed C–H Amidation Using Aroyloxycarbamates To Give N-Boc Protected Arylamines](https://d3i71xaburhd42.cloudfront.net/98c9a3cd058c85196f1280c6a72d4f2027b274a1/3-Table2-1.png)
Ortho vs ipso: site-selective Pd and norbornene-catalyzed arene
![Rh[III]-Catalyzed C–H Amidation Using Aroyloxycarbamates To Give N-Boc Protected Arylamines](https://pubs.rsc.org/image/article/2022/QO/d1qo01827b/d1qo01827b-u1_hi-res.gif)
N -Aroyloxycarbamates as switchable nitrogen and oxygen precursor
![Rh[III]-Catalyzed C–H Amidation Using Aroyloxycarbamates To Give N-Boc Protected Arylamines](https://d3i71xaburhd42.cloudfront.net/5f2f2c4df3eaf24310efa134e9fa0d96ac2151d2/2-Table2-1.png)
Iridium-catalyzed intermolecular amidation of sp³ C-H bonds: late
![Rh[III]-Catalyzed C–H Amidation Using Aroyloxycarbamates To Give N-Boc Protected Arylamines](https://pubs.rsc.org/image/article/2022/QO/d1qo01827b/d1qo01827b-s5_hi-res.gif)
N -Aroyloxycarbamates as switchable nitrogen and oxygen precursor
Tunable Arylative Cyclization of 1,6-Enynes Triggered by Rhodium
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