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Copper-Catalyzed Oxidative 1,2-Alkylarylation of Styrenes with Unactivated C(sp3)-H Alkanes and Electron-Rich Aromatics via C(sp3)-H/C(sp2)-H Functionalization
被引:11
|作者:
Jiang, Hui-Min
[1
]
Sun, Qing
[1
]
Jiang, Jin-Peng
[1
]
Qin, Jing-Hao
[1
]
Ouyang, Xuan-Hui
[1
]
Song, Ren-Jie
[1
]
机构:
[1] Nanchang Hangkong Univ, Key Lab Jiangxi Prov Persistent Pollutants Contro, Nanchang 330063, Jiangxi, Peoples R China
基金:
中国国家自然科学基金;
关键词:
alkenes;
copper-catalyzed;
alkanes;
C-H functionalization;
SP(3) C-H;
BOND FUNCTIONALIZATION;
DIFUNCTIONALIZATION;
ALKENES;
DICARBOFUNCTIONALIZATION;
ALKYLATION;
ALKYNES;
ACCESS;
ALKYLARYLATION;
ANNULATION;
D O I:
10.1002/adsc.202200548
中图分类号:
O69 [应用化学];
学科分类号:
081704 ;
摘要:
We have disclosed an alkenes dicarbofunctionalization method to introduce alkyl and electron-rich aryl across the C=C bond of styrenes under copper catalyst and oxidative conditions, leading to construct C(sp(3))-C(sp(2))/C(sp(3))-C(sp(3)) bonds via dual C-H functionalization. This method realizes the synthesis of 1,1-diarylalkanes, which are very important skeleton in natural products and drug molecules, through the grafting of electron-rich aromatics, including indoles, pyrroles, trisubstituted aromatic.
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页码:2772 / 2782
页数:11
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