Rh[III]-Catalyzed C–H Amidation Using Aroyloxycarbamates To Give N-Boc Protected Arylamines
Por um escritor misterioso
Last updated 31 março 2025
Christoph Grohmann - Senior Scientist, II - Firefly Biologics
![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-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.acs.org/cms/10.1021/ja211110h/asset/images/medium/ja-2011-11110h_0010.gif)
Mechanism of the Rhodium(III)-Catalyzed Arylation of Imines via C
Tunable Arylative Cyclization of 1,6-Enynes Triggered by Rhodium
![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://pubs.acs.org/cms/10.1021/jo5008515/asset/images/medium/jo-2014-008515_0003.gif)
Rhodium(III)-Catalyzed Intermolecular Amidation with Azides via C
![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://europepmc.org/articles/PMC3850750/bin/nihms-528975-f0004.jpg)
Microwave-assisted protection of primary amines as 2,5
![Rh[III]-Catalyzed C–H Amidation Using Aroyloxycarbamates To Give N-Boc Protected Arylamines](https://pubs.acs.org/cms/10.1021/acs.orglett.9b02625/asset/images/medium/ol9b02625_0002.gif)
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](https://pubs.acs.org/cms/10.1021/jo5003592/asset/images/medium/jo-2014-003592_0005.gif)
Cu-Catalyzed Direct Amidation of Aromatic C–H Bonds: An Access to
![Rh[III]-Catalyzed C–H Amidation Using Aroyloxycarbamates To Give N-Boc Protected Arylamines](https://pubs.acs.org/cms/10.1021/acs.orglett.9b02625/asset/images/medium/ol9b02625_0004.gif)
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](https://pubs.acs.org/cms/10.1021/acs.orglett.2c01780/asset/images/medium/ol2c01780_0008.gif)
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://d3i71xaburhd42.cloudfront.net/5f2f2c4df3eaf24310efa134e9fa0d96ac2151d2/3-Table4-1.png)
Table 4 from Iridium-catalyzed intermolecular amidation of sp³ C-H
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