Literature DB >> 16358295

Towards the automatic analysis of NMR spectra: part 6. Confirmation of chemical structure employing both 1H and 13C NMR spectra.

Lee Griffiths1, Rob Horton.   

Abstract

A method of comparing predicted and experimental chemical shifts was used to confirm or refute postulated structures. 1H NMR spectra returned all true positives with a false positive rate of 4%. When an analogous procedure was adopted for 13C NMR spectra, the false positive rate dropped to 1%, whereas the more practical HSQC data yielded a false positive rate of 2%. If the HSQC results were combined with 1H results, a false positive rate of 1% resulted, 4 times more accurate than 1H alone. Copyright 2005 John Wiley & Sons, Ltd.

Entities:  

Year:  2006        PMID: 16358295     DOI: 10.1002/mrc.1736

Source DB:  PubMed          Journal:  Magn Reson Chem        ISSN: 0749-1581            Impact factor:   2.447


  1 in total

1.  Identification of organic molecules from a structure database using proton and carbon NMR analysis results.

Authors:  Reinhard Dunkel; Xinzi Wu
Journal:  J Magn Reson       Date:  2007-06-30       Impact factor: 2.229

  1 in total

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