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通过X射线晶体学和1H NMR各向异性确定绝对构型。

Determination of absolute configurations by X-ray crystallography and 1H NMR anisotropy.

作者信息

Harada Nobuyuki

机构信息

Department of Chemistry, Columbia University, New York 10027, USA.

出版信息

Chirality. 2008 May 15;20(5):691-723. doi: 10.1002/chir.20478.

Abstract

To determine the absolute configurations of chiral compounds, many spectroscopic and diffraction methods have been developed. Among them, X-ray crystallographic Bijvoet method, CD exciton chirality method, and the combination of vibrational circular dichroism and quantum mechanical calculations are of nonempirical nature. On the other hand, X-ray crystallography using a chiral internal reference, and 1H NMR spectroscopy using chiral anisotropy reagents are relative and/or empirical methods. In addition to absolute configurational determinations, preparations of enantiopure compounds are strongly desired. As chiral reagents useful for both the preparation of enantiopure compounds by HPLC separation and the simultaneous determination of their absolute configurations, we have developed camphorsultam dichlorophthalic acid (CSDP acid) for X-ray crystallography and 2-methoxy-2-(1-naphthyl)propionic acid (MalphaNP acid) for 1H NMR spectroscopy. In this review, the principles and applications of these X-ray and NMR methods are explained using mostly our own data.

摘要

为了确定手性化合物的绝对构型,人们已经开发了许多光谱和衍射方法。其中,X射线晶体学的比沃伊特方法、圆二色激子手性方法以及振动圆二色性与量子力学计算相结合的方法具有非经验性质。另一方面,使用手性内参的X射线晶体学方法以及使用手性各向异性试剂的1H NMR光谱法是相对和/或经验方法。除了绝对构型的测定外,对映体纯化合物的制备也备受期待。作为可用于通过HPLC分离制备对映体纯化合物以及同时测定其绝对构型的手性试剂,我们开发了用于X射线晶体学的樟脑磺内酰胺二氯邻苯二甲酸(CSDP酸)和用于1H NMR光谱的2-甲氧基-2-(1-萘基)丙酸(MalphaNP酸)。在本综述中,这些X射线和NMR方法的原理及应用主要使用我们自己的数据进行解释。

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