冯手性N,N′-二氧化物配体的独特性及其影响

Dian-Feng Chen , Liu-Zhu Gong
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引用次数: 0

摘要

从历史的角度来看,所有被广泛接受的特权手性配体都会调节它们形成的金属配合物的催化活性,并赋予不对称反应立体选择性,仅依赖于与磷、氮或杂原子杂化物的配位。如今,与N,N'-二氧化酰胺(即Feng配体)的合作打破了这一传统,并表明氧配位配体也可以被优先使用,从而允许手性金属催化剂的增殖和高度对映选择性的转化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Feng chiral N,N′-dioxide ligands: uniqueness and impacts

Feng chiral N,N′-dioxide ligands: uniqueness and impacts

From the historical perspective, all widely accepted privileged chiral ligands tune the catalytic activity of the metal complexes that they form and impart stereoselectivity to asymmetric reactions exclusively relying on the coordination with phosphorus, nitrogen or hetero-atom hybrids. Nowadays, works with N,N’-dioxide amides, i.e., Feng ligands, break with this tradition and have shown that oxygen-coordinated ligands can also be privileged, allowing for the proliferation of chiral metal catalysts and highly enantioselective transformations.

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