"Cofactor"-Controlled Enantioselective Catalysis

被引:98
|
作者
Dydio, Pawel [1 ]
Rubay, Christophe [1 ]
Gadzikwa, Tendai [1 ]
Lutz, Martin [2 ]
Reek, Joost N. H. [1 ]
机构
[1] Univ Amsterdam, Vant Hoff Inst Mol Sci, NL-1098 XH Amsterdam, Netherlands
[2] Univ Utrecht, Bijvoet Ctr Biomol Res, NL-3584 CH Utrecht, Netherlands
关键词
SUPRAMOLECULAR CATALYSIS; SIGNAL AMPLIFICATION; BIDENTATE LIGANDS; HIGH-THROUGHPUT; TRANSITION; CHEMISTRY; MODELS; RECEPTORS; LIBRARIES; DESIGN;
D O I
10.1021/ja208589c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We report an achiral bisphosphine rhodium complex with a binding site for the recognition of chiral anion guests. Upon binding small chiral guests-cofactors-the rhodium complex becomes chiral and can thus be used for asymmetric catalysis. Screening of a library of cofactors revealed that the best cofactors lead to hydrogenation catalysts that form the products with high enantioselectivity (ee's up to 99%). Interestingly, a competition experiment shows that even in a mixture of 12 cofactors high ee is obtained, indicating that the complex based on the best cofactor dominates the catalysis.
引用
收藏
页码:17176 / 17179
页数:4
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