Manganese-Catalyzed ortho-C-H Alkenylation of Aromatic N-H Imidates with Alkynes: Versatile Access to Mono-Alkenylated Aromatic Nitriles

被引:94
作者
Yang, Xiaoxu [1 ]
Jin, Xiqing [1 ]
Wang, Congyang [1 ]
机构
[1] Chinese Acad Sci, Inst Chem, CAS Key Lab Mol Recognit & Funct, Beijing Natl Lab Mol Sci, Beijing 100190, Peoples R China
基金
中国国家自然科学基金;
关键词
alkynes; C-H activation; homogeneous catalysis; manganese; nitriles; 2+2+2 CYCLOADDITION; BOND FUNCTIONALIZATIONS; ACTIVATION; CONSTRUCTION; ALDEHYDES; ROUTE; ACID; CYCLOTRIMERIZATION; ALPHA; OMEGA-DIYNES; ARYLNITRILES;
D O I
10.1002/adsc.201600128
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
So far, the direct C-H alkenylation of aromatic nitriles with alkynes has not been achieved. Herein, we discribe the first manganese-catalyzed C-H alkenylation of aromatic N-H imidates to access mono-alkenylated aromatic nitriles. The reaction is accelerated by the presence of a catalytic amount of sodium pivalate. This protocol is also highlighted by the simple catalytic system, good compatibility of functional groups, and excellent mono-/dialkenylation selectivity as well as E/Z stereoselectivity.
引用
收藏
页码:2436 / 2442
页数:7
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