Recent Advances in Multinuclear NMR Spectroscopy for Chiral Recognition of Organic Compounds

M. Silva
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引用次数: 49

Abstract

Nuclear magnetic resonance (NMR) is a powerful tool for the elucidation of chemical structure and chiral recognition. In the last decade, the number of probes, media, and experiments to analyze chiral environments has rapidly increased. The evaluation of chiral molecules and systems has become a routine task in almost all NMR laboratories, allowing for the determination of molecular connectivities and the construction of spatial relationships. Among the features that improve the chiral recognition abilities by NMR is the application of different nuclei. The simplicity of the multinuclear NMR spectra relative to 1H, the minimal influence of the experimental conditions, and the larger shift dispersion make these nuclei especially suitable for NMR analysis. Herein, the recent advances in multinuclear (19F, 31P, 13C, and 77Se) NMR spectroscopy for chiral recognition of organic compounds are presented. The review describes new chiral derivatizing agents and chiral solvating agents used for stereodiscrimination and the assignment of the absolute configuration of small organic compounds.
有机化合物手性识别的多核磁共振光谱研究进展
核磁共振(NMR)是化学结构分析和手性识别的有力工具。在过去的十年中,用于分析手性环境的探针、介质和实验的数量迅速增加。手性分子和体系的评价已经成为几乎所有核磁共振实验室的常规任务,允许确定分子连通性和空间关系的构建。不同核的应用是提高核磁共振手性识别能力的一大特点。多核核谱相对于1H的简单性、实验条件的影响最小以及较大的位移色散使这些核特别适合于核磁共振分析。本文综述了多核(19F, 31P, 13C和77Se)核磁共振光谱手性识别有机化合物的最新进展。综述了用于小分子有机化合物立体识别和绝对构型配位的新型手性衍生化剂和手性溶剂化剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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