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首页> 外文期刊>Angewandte Chemie >Achieving Enantioselectivity with Chiral Cyclopeetadienylrhodium Complexes
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Achieving Enantioselectivity with Chiral Cyclopeetadienylrhodium Complexes

机译:用手性环戊二烯基铑配合物实现对映选择性

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摘要

A significant number of interesting otherwise hard-to-accomplish transformations can be catalyzed by half-sandwich complexes of transition metals, especially by complexes of late transition metals with a single cyclopentadienyl (Cp) or pentamethylcyclopentadienyl (Cp~*) ligand. While it is deceptively easy to conceive of and prepare chiral half-sandwich complexes, there are only few examples of late-transition-metal complexes that have been used successfully as enantio-selective catalysts. Recently, two different strategies have been employed to introduce chirality to rhodium Cp complexes, and their application as enantioselective catalysts for the formation of dihydroisoquinolones from benzamides and olefins has been demonstrated.
机译:过渡金属的半夹心络合物,尤其是晚期过渡金属与单个环戊二烯基(Cp)或五甲基环戊二烯基(Cp〜*)配体的络合物,可以催化大量有趣的否则难以实现的转化。尽管看似容易构想和制备手性半三明治配合物,但只有很少的例子成功地将对过渡金属配合物用作对映选择性催化剂。最近,已经采用了两种不同的策略将手性引入铑Cp络合物中,并且已经证明了它们作为对映选择性催化剂由苯甲酰胺和烯烃形成二氢异喹诺酮的应用。

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