Synthesis of Planar Chiral Ferrocenes by Transition-Metal-Catalyzed Enantioselective C-H Activation

被引:105
|
作者
Zhu, Dao-Yong [1 ]
Chen, Ping [2 ]
Xia, Ji-Bao [1 ]
机构
[1] Chinese Acad Sci, Lanzhou Inst Chem Phys, Suzhou Res Inst LICP, State Key Lab Oxo Synth & Select Oxidat, Lanzhou 730000, Peoples R China
[2] Nanyang Inst Technol, Dept Biochem Engn, Nanyang 473004, Peoples R China
关键词
C-H activation; enantioselective catalysis; ferrocenes; planar chirality; transition-metal catalysis; ASYMMETRIC-SYNTHESIS; BOND ACTIVATION; QUATERNARY STEREOCENTERS; KINETIC RESOLUTION; ORTHO-LITHIATION; LIGANDS; DERIVATIVES; SILYLATION; ALKYLATION; C(SP(2))-H;
D O I
10.1002/cctc.201500895
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
This minireview focuses on recent advancements in the synthesis of planar chiral ferrocenes by means of transition-metal-catalyzed enantioselective C-H activation. Enantioenriched planar chiral ferrocenes are synthesized through simple straightforward asymmetric carbon-carbon or carbon-hetero-atom bond-formation reactions. In these reports, site selectivity of ferrocene C-H activation is controlled by two strategies, coordination direction and intramolecular cyclization. Herein the significance of these results is summarized.
引用
收藏
页码:68 / 73
页数:6
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