Enantioselective Preparation of Planar-Chiral Transition Metal Complexes by Asymmetric Olefin-Metathesis Reactions in Metal Coordination Spheres

被引:7
|
作者
Ogasawara, Masamichi [1 ,2 ]
机构
[1] Tokushima Univ, Grad Sch Sci & Technol, Dept Nat Sci, 2-1 Minamijosanjima Cho, Tokushima 7708506, Japan
[2] Tokushima Univ, Tokushima Int Sci Inst, 2-1 Minamijosanjima Cho, Tokushima 7708506, Japan
来源
CHEMICAL RECORD | 2021年 / 21卷 / 12期
关键词
asymmetric catalysis; desymmetrization; kinetic resolution; olefin metathesis; planar chirality; RING-CLOSING METATHESIS; LIPASE-MEDIATED RESOLUTION; KINETIC RESOLUTION; ORTHO-LITHIATION; MOLYBDENUM; FERROCENES; CATALYSIS; LIGANDS; DERIVATIVES; 1,4-ADDITION;
D O I
10.1002/tcr.202100102
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Planar-chiral transition metal complexes are useful chiral auxiliaries in organic and organometallic chemistry, and they have been utilized as chiral ligands, chiral catalysts, or chiral building blocks, etc. Despite the importance of such planar-chiral species in asymmetric synthesis, their preparation in optically active forms is still a challenging problem. Indeed, reported examples of catalytic enantioselective synthesis of planar-chiral complexes have been rare, and this has been a developing area in this field. In this personal account, recent results from our research group on the catalytic asymmetric synthesis of various planar-chiral transition metal complexes are summarized. The asymmetric ring-closing metathesis reactions catalyzed by the well-defined molybdenum-alkylidene species are powerful methods to control the planar chirality in ferrocenes, ruthenocenes, (eta(6)-arene)chromium complexes, and (eta(5)-cyclopentadienyl)manganese(I) complexes. Application of the enantiomerically enriched complexes obtained by our methods is described as well.
引用
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页码:3509 / 3519
页数:11
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