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Asymmetric Synthesis of Silicon-Stereogenic Vinylhydrosilanes by Cobalt-Catalyzed Regio- and Enantioselective Alkyne Hydrosilylation with Dihydrosilanes
被引:145
|作者:
Wen, Huanan
[1
]
Wan, Xiaolong
[1
]
Huang, Zheng
[1
]
机构:
[1] Chinese Acad Sci, Univ Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Organometall Chem,Ctr Excellence Mo, 345 Lingling Rd, Shanghai 200032, Peoples R China
关键词:
asymmetric catalysis;
cobalt;
hydrosilylation;
silicon-stereogenic compounds;
vinylsilanes;
DEHYDROGENATIVE SILYLATION;
ALKENE HYDROSILYLATION;
MARKOVNIKOV HYDROSILYLATION;
RHODIUM COMPLEXES;
TERTIARY SILANES;
TERMINAL ALKYNES;
IRON CATALYSTS;
BOND;
DESYMMETRIZATION;
CONSTRUCTION;
D O I:
10.1002/anie.201802806
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
The strategic carbon-to-silicon substitution at a stereogenic center can produce chiral silanes with significantly improved properties relative to their carbon congeners. We herein report an unprecedented cobalt-catalyzed asymmetric hydrosilylation of unsymmetric alkynes with dihydrosilanes that furnishes silicon-stereogenic vinylhydrosilanes with high regio- and enantioselectivity. The absolute configurations of the products were determined by chiroptical methods in combination with DFT calculations. The synthetic versatility of the vinylhydrosilanes as chiral building blocks was further demonstrated by asymmetric Si-H insertion and catalytic hydroboration reactions.
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页码:6319 / 6323
页数:5
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