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手性含吡啶大环配体(Pc-L*)的 Cu(I) 配合物催化的烯烃不对称环丙烷化。

Asymmetric cyclopropanation of olefins catalysed by Cu(I) complexes of chiral pyridine-containing macrocyclic ligands (Pc-L*).

机构信息

Dipartimento di Chimica, Università di Milano, Via Golgi 19, 20133 Milano, Italy.

出版信息

Dalton Trans. 2013 Feb 21;42(7):2451-62. doi: 10.1039/c2dt32347h. Epub 2012 Dec 3.

Abstract

The synthesis and characterisation of copper(I) complexes of chiral pyridine-containing macrocyclic ligands (Pc-L*) and their use as catalysts in asymmetric cyclopropanation reactions are reported. All ligands and metal complexes were fully characterised, including crystal structures of some species determined by X-ray diffraction on single crystals. This allowed characterising the very different conformations of the macrocycles which could be induced by different substituents or by metal complexation. The strategy adopted for the ligand synthesis is very flexible allowing several structural modifications. A small library of macrocyclic ligands possessing the same donor properties but with either C(1) or C(2) symmetry was synthesized. Cyclopropane products with both aromatic and aliphatic olefins were obtained in good yields and enantiomeric excesses up to 99%.

摘要

本文报道了手性含吡啶大环配体(Pc-L*)的铜(I)配合物的合成与表征,以及它们在手性环丙烷化反应中的催化应用。所有配体和金属配合物都经过了充分的表征,包括通过单晶 X 射线衍射确定了某些物种的晶体结构。这使得可以对大环的非常不同构象进行表征,这些构象可以由不同的取代基或金属络合诱导。所采用的配体合成策略非常灵活,可以进行多种结构修饰。合成了具有相同供体性质但具有 C(1)或 C(2)对称性的大环配体的小文库。芳香族和脂肪族烯烃的环丙烷产物均以良好的收率和高达 99%的对映体过量值获得。

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