Iridium-Catalyzed Enantioselective Hydrogenation of Vinylsilanes

被引:17
|
作者
Wang, Aie [1 ,2 ]
Bernasconi, Maurizio [2 ]
Pfaltz, Andreas [2 ]
机构
[1] Xiamen Univ, Dept Chem, Coll Chem, Fujian Prov Key Lab Chem Biol, Xiamen 361005, Fujian, Peoples R China
[2] Univ Basel, Dept Chem, St Johanns Ring 19, CH-4056 Basel, Switzerland
基金
瑞士国家科学基金会;
关键词
asymmetric hydrogenation; iridium; N; P ligands; vinylsilanes; CONJUGATE SILYL TRANSFER; CROSS-COUPLING REACTION; SI BOND FORMATION; ASYMMETRIC HYDROGENATION; ALLYLIC SUBSTITUTION; ORGANOSILICON COMPOUNDS; OXAZOLINE LIGANDS; ORGANIC-SYNTHESIS; CARBON BOND; ALLYLSILANES;
D O I
10.1002/adsc.201700162
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
We have screened a diverse array of iridium complexes derived from chiral N,P ligands as catalysts for the asymmetric hydrogenation of vinylsilanes, a transformation for which generally applicable catalysts were lacking. Several catalysts emerged from this study that enabled the highly enantioselective hydrogenation of a wide range of vinylsilanes with trisubstituted or disubstituted terminal C=C bonds bearing aryl, alkyl, ethoxycarbonyl, or hydroxymethyl substituents. In addition to trimethylsilyl and dimethyl(phenyl) silyl derivatives, trialkoxysilyl- and silacyclobutyl-substituted alkenes were used as substrates.
引用
收藏
页码:2523 / 2529
页数:7
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