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://onlinelibrary.wiley.com/cms/asset/44158c0a-8c87-4218-88e0-b39a32f992a9/cjoc202100430-fig-0003-m.jpg)
Selective Carbon‐Carbon Bond Amination with Redox‐Active Aminating
![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/jo5003592/asset/images/medium/jo-2014-003592_0007.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.rsc.org/image/article/2022/QO/d1qo01827b/d1qo01827b-s3_hi-res.gif)
N -Aroyloxycarbamates as switchable nitrogen and oxygen precursor
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.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.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://pubs.rsc.org/image/article/2022/OB/d2ob01157c/d2ob01157c-s31.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.rsc.org/image/article/2022/OB/d2ob01157c/d2ob01157c-s24_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](http://sioc-journal.cn/Jwk_yjhx/fileup/0253-2786/PIC/1646395291936-392794653_pic.jpg)
Rhodium(III) Catalyzed C(sp3)—H Functionalization
![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://d3i71xaburhd42.cloudfront.net/89c19c69cbc2ada3b7686478b2195c277c416f8c/3-Table2-1.png)
Ru(II)-catalyzed amidation reactions of 8-methylquinolines with
![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://pubs.acs.org/cms/10.1021/cs501860b/asset/images/medium/cs-2014-01860b_0010.gif)
Cobalt(III)-Catalyzed C–H Amidation of Arenes using
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