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首页> 外文期刊>Angewandte Chemie >Highly Rigid Diphosphane Ligands with a Large Dihedral Angle Based on a Chiral Spirobifluorene Backbone
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Highly Rigid Diphosphane Ligands with a Large Dihedral Angle Based on a Chiral Spirobifluorene Backbone

机译:基于手性螺螺芴骨架的大二面角高刚性二膦烷配体

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摘要

Asymmetric catalysis is undoubtedly a powerful, economically feasible tool for the synthesis of optically active organic compounds both in the laboratory and on a production scale. The design and synthesis of chiral phosphane ligands have played a significant role in the development of efficient, transition-metal-catalyzed asymmetric reactions.[1] In the last decades, a large number of chiral diphosphane ligands, such as diop,[2] binap,[3] josiphos,[4] duphos,[5] pennphos,[6] bisp,[7] p-phos,[8] and tangphos,[9] have been prepared and used in asymmetric catalysis with excellent enantioselectivities. Since there are no universal ligands and catalysts for asymmetric transformations, and most asymmetric reactions are substrate dependent, the search for chiral ligands that are more efficient in terms of high enantioselectivity and high turnover number (TON) remains one of the most important goals in asymmetric catalysis.
机译:无论在实验室还是在生产规模上,不对称催化无疑是一种强大的,经济上可行的工具,用于合成旋光有机化合物。手性膦配体的设计和合成在有效的过渡金属催化不对称反应的发展中起着重要作用。[1]在过去的几十年中,大量的手性二膦配体,例如diop,[2] binap,[3] josiphos,[4] duphos,[5] pennphos,[6] bisp,[7] p-phos,[ [8]和tangphos,[9]已经制备出来并用于不对称催化,具有出色的对映选择性。由于不存在用于不对称转化的通用配体和催化剂,并且大多数不对称反应均依赖于底物,因此寻求在高对映选择性和高周转数(TON)方面更有效的手性配体仍然是不对称的最重要目标之一催化。

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