Nickel/NHC-Catalyzed Asymmetric C-H Alkylation of Fluoroarenes with Alkenes: Synthesis of Enantioenriched Fluorotetralins

被引:73
作者
Cai, Yuan [1 ]
Ye, Xiaodong [1 ]
Liu, Sheng [1 ]
Shi, Shi-Liang [1 ]
机构
[1] Univ Chinese Acad Sci, Ctr Excellence Mol Synth, Shanghai Inst Organ Chem, Chinese Acad Sci,State Key Lab Organometall Chem, 345 Lingling Lu, Shanghai 200032, Peoples R China
关键词
asymmetric hydroarylation; C-H alkylation; chiral NHC ligand; fluoroarenes; nickel catalysis; BOND ACTIVATION; HYDROARYLATION; HYDROHETEROARYLATION; POLYFLUOROARENES; ALKENYLATION; ARYLATION; ECONOMY; HYDRODEFLUORINATION; BORYLATION; STYRENES;
D O I
10.1002/anie.201907387
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Chiral polyfluoroarene derivatives are an important scaffold in chemistry. An unprecedented enantioselective C-H alkylation of polyfluoroarenes with alkenes is described. The reaction employs bulky chiral N-heterocyclic carbene (NHC) ligands for nickel catalysts to enable exclusive activation of C-H bonds over C-F bonds and complete endo-selective C-H annulation and excellent enantioselectivity. A wide variety of chiral fluorotetralins, compounds otherwise difficultly accessed but serve as important bioisosteric analogs of both tetralin and heterocycle units for drug design, are expediently synthesized from easily available substrates. To our knowledge, this is the first example of catalytic enantioselective C-H functionalization of polyfluoroarenes.
引用
收藏
页码:13433 / 13437
页数:5
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