Transition-Metal-Assisted Radical/Radical Cross-Coupling: A New Strategy to the Oxidative C(sp3)-H/N-H Cross-Coupling

被引:151
|
作者
Zhou, Liangliang [1 ]
Tang, Shan [1 ]
Qi, Xiaotian [2 ]
Lin, Caitao [1 ]
Liu, Kun [1 ]
Liu, Chao [1 ]
Lan, Yu [2 ]
Lei, Aiwen [1 ]
机构
[1] Wuhan Univ, Coll Chem & Mol Sci, Wuhan 430072, Hubei, Peoples R China
[2] Chongqing Univ, Sch Chem & Chem Engn, Chongqing 400030, Peoples R China
基金
高等学校博士学科点专项科研基金; 中国国家自然科学基金;
关键词
C-H AMINATION; COPPER-CATALYZED AMIDATION; NITROGEN BOND FORMATION; REDUCTIVE-ELIMINATION; EFFICIENT SYNTHESIS; CARBON; CYCLIZATION; ADJACENT; ETHERS; RUTHENIUM;
D O I
10.1021/ol501485f
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A transition-metal-assisted oxidative C(sp(3))-H/N-H cross-coupling reaction of N-alkoxyamides with aliphatic hydrocarbons is described. During the reaction, nitrogen radicals were generated from the oxidation of N-alkoxyamides. Experiments and DFT calculations revealed that transition-metal catalyst could lower the reactivity of the generated nitrogen radical by the coordination of the transition metal, which allowed the selective radical/radical cross-coupling with the transient sp(3) carbon radical to construct C(sp(3))--N bonds. Various C(sp(3))-H bonds could be transformed into C(sp(3))-N bonds through this radical amidation strategy.
引用
收藏
页码:3404 / 3407
页数:4
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