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Enantioselective Construction of Silicon-Stereogenic Silanes by Scandium-Catalyzed Intermolecular Alkene Hydrosilylation
被引:99
|作者:
Zhan, Gu
[1
]
Teng, Huai-Long
[2
]
Luo, Yong
[1
]
Lou, Shao-Jie
[2
]
Nishiura, Masayoshi
[1
,2
]
Hou, Zhaomin
[1
,2
]
机构:
[1] RIKEN, Cluster Pioneering Res, Organometall Chem Lab, 2-1 Hirosawa, Wako, Saitama 3510198, Japan
[2] RIKEN, Ctr Sustainable Resource Sci, Adv Catalysis Res Grp, 2-1 Hirosawa, Wako, Saitama 3510198, Japan
关键词:
asymmetric catalysis;
hydrosilylation;
rare earths;
scandium;
silicon-stereogenic silanes;
ASYMMETRIC-SYNTHESIS;
C-H;
METAL-COMPLEXES;
DESYMMETRIZATION;
SILYLATION;
CHEMISTRY;
FUNCTIONALIZATION;
DIBENZOSILOLES;
DERIVATIVES;
YTTRIUM;
D O I:
10.1002/anie.201807493
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
The catalytic asymmetric construction of silicon-stereogenic silanes is of great interest and significance, but has met with only limited success to date. We herein report the enantioselective hydrosilylation of alkenes with dihydrosilanes by a chiral half-sandwich scandium catalyst, which constitutes an efficient and general route for the synthesis of a wide range of enantioenriched silicon-stereogenic silanes from easily accessible starting materials. This reaction features a broad substrate scope, high yields, and high enantioselectivity. Some of the chiral tertiary silane products were also converted into valuable derivatives, such as chiral silanol, quaternary silane, and benzosilole compounds.
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页码:12342 / 12346
页数:5
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