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Ni-Catalyzed Intermolecular C(sp(3))-H Amidation Tuned by Bidentate Directing Groups

Authors
Kim, Yeong BumWon, JoongheeLee, JeonghyoKim, JunhoZhou, BingweiPark, Jung-WooBaik, Mu-HyunChang, Sukbok
Issue Date
Mar-2021
Publisher
AMER CHEMICAL SOC
Keywords
nickel catalysis; C(sp(3))-H amidation; organic azides; 8-aminoquinolines; electronic tuning
Citation
ACS CATALYSIS, v.11, no.5, pp.3067 - 3072
Indexed
SCIE
SCOPUS
Journal Title
ACS CATALYSIS
Volume
11
Number
5
Start Page
3067
End Page
3072
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/189283
DOI
10.1021/acscatal.1c00070
ISSN
21555435
Abstract
We disclose herein a directing group-assisted nickel-catalyzed intermolecular C(sp(3))-H amidation using organic azides as nitrene precursors. With the installation of an electronically tailored directing group, enhanced amidation efficiency was achieved. A series of experimental and computational studies suggested that a putative nickel(III)-nitrenoid species is a key intermediate in the C-N bond-forming process.
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