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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.
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页码:2523 / 2529
页数:7
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