期刊
ACS CATALYSIS
卷 -, 期 -, 页码 -出版社
AMER CHEMICAL SOC
DOI: 10.1021/acscatal.2c02872
关键词
cobalt; maleimide; monocyclic olefin mediator; C-H functionalization; ortho-amidation
资金
- Department of Atomic Energy (DAE)
- Science and Engineering Research Board (SERB) , New Delhi [CRG/2021/007153]
- SERB
- DST INSPIRE
- US National Science Foundation [CHE-1856416, CHE-030089]
- Croucher Foundation
- NISER, Department of Atomic Energy (DAE)
A catalytic system has been discovered for the intramolecular C-H amidation of N-phenoxy acetamide derivatives. The use of a cobalt catalyst and maleimide as a transient mediator enables the olefin-mediated ortho C-H functionalization. Mechanistic and DFT studies provide support for the proposed mechanism. The products derived from this methodology have been demonstrated as ligands in the C-H olefination reaction.
A catalytic system is discovered for the intramolecular C-H amidation of N-phenoxy acetamide derivatives. Herein, a cobalt catalyst has been employed for the olefin-mediated ortho C-H functionalization. Moreover, a monocyclic olefin, maleimide, has been used as a transient mediator instead of well-established bicyclic norbornenes. Maleimide promotes a Co(III) intermediate to undergo oxidative addition into the O-N bond to form a Co(V) nitrene species and subsequently directs nitrene addition to the ortho position. Mechanistic study and density functional theory (DFT) study support the proposed mechanism. The products derived from this methodology have been demonstrated as a ligand in the C-H olefination reaction. Furthermore, the synthetic utility of this methodology was demonstrated via the ortho-amidation of estrone.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据