Literature DB >> 6866719

Distinction between the tautomeric forms of sulfanilamide derivatives by 13C-NMR.

A Bult.   

Abstract

The application of 13C-NMR for the distinction between amido and imido tautomers of sulfanilamide derivatives in DMSO solution is described. The differentiation is based on delta delta, the change in chemical shift of a sulfanilamide from the neutral form (in DMSO solution) to the anion (in aqueous alkaline solution). The delta delta values of three C atoms (C1, C1', C4) are suitable for the differentiation between the tautomers. The conclusions confirm previous results.

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Year:  1983        PMID: 6866719     DOI: 10.1007/bf01960081

Source DB:  PubMed          Journal:  Pharm Weekbl Sci        ISSN: 0167-6555


  1 in total

1.  Carbon-13 magnetic resonance spectroscopy of drugs. Sulfonamides.

Authors:  C Chang; H G Floss; G E Peck
Journal:  J Med Chem       Date:  1975-05       Impact factor: 7.446

  1 in total
  1 in total

1.  Experimental Electron Density and Neutron Diffraction Studies on the Polymorphs of Sulfathiazole.

Authors:  Ioana Sovago; Matthias J Gutmann; J Grant Hill; Hans Martin Senn; Lynne H Thomas; Chick C Wilson; Louis J Farrugia
Journal:  Cryst Growth Des       Date:  2014-01-17       Impact factor: 4.076

  1 in total

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