Literature DB >> 26385260

A Simple ¹³C NMR Method for the Discrimination of Complex Mixtures of Stereoisomers: All Eight Stereoisomers of α-Tocopherol Resolved.

Peter P Lankhorst1, Thomas Netscher2, Alexander L L Duchateau1.   

Abstract

A simple one-dimensional (13)C NMR method is presented to discriminate between stereoisomers of organic compounds with more than one chiral center. By means of this method it is possible to discriminate between all eight stereoisomers of α-tocopherol. To achieve this the chiral solvating agent (S)-(+)-1-(9-anthryl)-2,2,2-trifluoroethanol and the compound of interest were dissolved in high concentrations in chloroform-d, and the nuclear magnetic resonance (NMR) spectrum was recorded at a low temperature. The individual stereoisomers of α-tocopherol were assigned by spikes of the reference compounds. The method was also applied to six other representative examples.
© 2015 Wiley Periodicals, Inc.

Entities:  

Keywords:  Pirkle's alcohol; TFAE; diastereoisomers; enantiomers; vitamin E

Mesh:

Substances:

Year:  2015        PMID: 26385260     DOI: 10.1002/chir.22535

Source DB:  PubMed          Journal:  Chirality        ISSN: 0899-0042            Impact factor:   2.437


  2 in total

Review 1.  Recent Advances in Multinuclear NMR Spectroscopy for Chiral Recognition of Organic Compounds.

Authors:  Márcio S Silva
Journal:  Molecules       Date:  2017-02-07       Impact factor: 4.411

2.  One-Dimensional 13C NMR Is a Simple and Highly Quantitative Method for Enantiodiscrimination.

Authors:  Peter P Lankhorst; Jozef H J van Rijn; Alexander L L Duchateau
Journal:  Molecules       Date:  2018-07-20       Impact factor: 4.411

  2 in total

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