Rh[III]-Catalyzed C–H Amidation Using Aroyloxycarbamates To Give N-Boc Protected Arylamines
Por um escritor misterioso
Last updated 29 março 2025
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](https://pubs.acs.org/cms/10.1021/ol401569u/asset/images/large/ol-2013-01569u_0006.jpeg)
Rhodium(III)-Catalyzed C–H Activation and Amidation of Arenes
![Rh[III]-Catalyzed C–H Amidation Using Aroyloxycarbamates To Give N-Boc Protected Arylamines](https://onlinelibrary.wiley.com/cms/asset/82b9544a-5f43-4aa0-94aa-a6505668911c/anie201808159-fig-5051-m.png)
Rhodium‐Catalyzed C(sp2)‐ or C(sp3)−H Bond Functionalization
![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
Christoph Grohmann - Senior Scientist, II - Firefly Biologics
![Rh[III]-Catalyzed C–H Amidation Using Aroyloxycarbamates To Give N-Boc Protected Arylamines](https://d3i71xaburhd42.cloudfront.net/5f2f2c4df3eaf24310efa134e9fa0d96ac2151d2/2-Table3-1.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-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://pubs.rsc.org/image/article/2022/OB/d2ob01157c/d2ob01157c-s17_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://pub.mdpi-res.com/molecules/molecules-20-10910/article_deploy/html/images/molecules-20-10910-g002.png?1569012387)
Molecules, Free Full-Text
![Rh[III]-Catalyzed C–H Amidation Using Aroyloxycarbamates To Give N-Boc Protected Arylamines](https://pubs.rsc.org/image/article/2022/OB/d2ob01157c/d2ob01157c-s31.gif)
Directing group strategies in rhodium-catalyzed C–H amination
Rhodium(III)-Catalyzed Intermolecular Amidation with Azides via C
![Rh[III]-Catalyzed C–H Amidation Using Aroyloxycarbamates To Give N-Boc Protected Arylamines](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/7e50097f-41d5-4669-896c-2bb41decde69/cctc201600079-fig-5013-m.png)
Directing‐Group‐Assisted Transition‐Metal‐Catalyzed Direct
![Rh[III]-Catalyzed C–H Amidation Using Aroyloxycarbamates To Give N-Boc Protected Arylamines](https://pubs.acs.org/cms/10.1021/ol401569u/asset/images/medium/ol-2013-01569u_0002.gif)
Rhodium(III)-Catalyzed C–H Activation and Amidation of Arenes
![Rh[III]-Catalyzed C–H Amidation Using Aroyloxycarbamates To Give N-Boc Protected Arylamines](https://pubs.acs.org/cms/10.1021/ol900298e/asset/images/large/ol-2009-00298e_0009.jpeg)
Direct Amination of Azoles via Catalytic C−H, N−H Coupling
![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
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