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超分子纳米胶囊内选择性保护控制的立体异构体的动力学拆分。

Kinetic resolution of constitutional isomers controlled by selective protection inside a supramolecular nanocapsule.

机构信息

Department of Chemistry, University of New Orleans, New Orleans, Louisiana 70148, USA.

出版信息

Nat Chem. 2010 Oct;2(10):847-52. doi: 10.1038/nchem.751. Epub 2010 Aug 8.

Abstract

The concept of self-assembling container molecules as yocto-litre reaction flasks is gaining prominence. However, the idea of using such containers as a means of protection is not well developed. Here, we illustrate this idea in the context of kinetic resolutions. Specifically, we report on the use of a water-soluble, deep-cavity cavitand to bring about kinetic resolutions within pairs of esters that otherwise cannot be resolved because they react at very similar rates. Resolution occurs because the presence of the cavitand leads to a competitive binding equilibrium in which the stronger binder primarily resides inside the host and the weaker binding ester primarily resides in the bulk hydrolytic medium. For the two families of ester examined, the observed kinetic resolutions were highest within the optimally fitting smaller esters.

摘要

作为微升反应瓶的自组装容器分子的概念越来越受到关注。然而,将此类容器用作保护手段的想法还没有得到很好的发展。在这里,我们在动力学拆分的背景下说明了这个想法。具体来说,我们报告了使用一种水溶性的、深腔的主体来实现一对酯的动力学拆分,否则这对酯无法拆分,因为它们的反应速率非常相似。拆分发生是因为主体的存在导致了一个竞争结合平衡,其中较强的配体主要存在于主体内部,较弱的结合酯主要存在于体积较大的水解介质中。在所研究的两类酯中,在最佳拟合的较小酯中观察到的动力学拆分最高。

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