Catalytic Enantioselective Synthesis of Silicon-Stereogenic Alkoxysilanes and Siloxanes

被引:11
|
作者
Zhu, Jiefeng [1 ,2 ,3 ]
He, Chuan [1 ,2 ]
机构
[1] Southern Univ Sci & Technol, Shenzhen Grubbs Inst, Shenzhen 518055, Guangdong, Peoples R China
[2] Southern Univ Sci & Technol, Dept Chem, Guangdong Prov Key Lab Catalysis, Shenzhen 518055, Guangdong, Peoples R China
[3] Harbin Inst Technol, Sch Chem & Chem Engn, Harbin 150080, Peoples R China
基金
中国国家自然科学基金;
关键词
asymmetric catalysis; dehydrogenative Si-O coupling; sillcon-stereogenic alkoxysilanes; silicon-stereogenic siloxanes; CPL-active silanes; CIRCULARLY-POLARIZED LUMINESCENCE; ASYMMETRIC-SYNTHESIS; ORGANOSILICON COMPOUNDS; SILANES; ACCESS; HYDROSILYLATION; CONSTRUCTION; ALCOHOLYSIS; SILYLATIONS; KETONES;
D O I
10.1055/a-1503-7976
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A Rh-catalyzed enantioselective intermolecular dehydrogenative Si-O coupling of dihydrosilanes with alcohols and silanols is demonstrated. Rh(I) catalyst equipped with a Josiphos ligand enables the highly enantioselective alcoholysis process of dihydrosilanes, giving access to a variety of functionalized triorgano-substituted silicon-stereogenic alkoxysilanes and siloxanes in decent yields and ee, which significantly expand the chemical space of the silicon-centered chiral molecules. Utility of this methodology is illustrated by the construction of circularly polarized luminescence (CPL) active chiral alkoxysilane small organic molecules.
引用
收藏
页码:1575 / 1580
页数:6
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