Asymmetric catalysis based on tropos ligands

被引:52
作者
Aikawa, Kohsuke [1 ]
Mikami, Koichi [1 ]
机构
[1] Tokyo Inst Technol, Dept Appl Chem, Meguro Ku, Tokyo 1528552, Japan
关键词
BIPHENYLPHOSPHINE BIPHEP LIGAND; DIELS-ALDER REACTIONS; ENE-TYPE CYCLIZATION; ENANTIOSELECTIVE INTRAMOLECULAR HYDROAMINATION; DICATIONIC PALLADIUM(II) COMPLEXES; ENANTIOMER-SELECTIVE ACTIVATION; ACHIRAL BENZOPHENONE LIGAND; TRANSITION-METAL CATALYSIS; AXIAL CHIRALITY CONTROL; BOND-FORMING REACTIONS;
D O I
10.1039/c2cc34320g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
All enantiopure atropisomeric (atropos) ligands essentially require enantiomeric resolution or synthetic transformation from a chiral pool. In sharp contrast, the use of tropos (chirally flexible) ligands, which are highly modular, versatile, and easy to synthesize without enantiomeric resolution, has recently been the topic of much interest in asymmetric catalysis. Racemic catalysts bearing tropos ligands can be applied to asymmetric catalysis through enantiomeric discrimination by the addition of a chiral source, which preferentially transforms one catalyst enantiomer into a highly activated catalyst enantiomer. Additionally, racemic catalysts bearing tropos ligands can also be utilized as atropos enantiopure catalysts obtained via the control of chirality by a chiral source followed by the memory of chirality. In this feature article, our results on the asymmetric catalysis via the combination of various central metals and tropos ligands are summarized.
引用
收藏
页码:11050 / 11069
页数:20
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