NMR studies of the conformational behaviour and tautomerism of bis- And tris-saccharidoguanidines

Gábor Tóth, Tamás Gáti, István Pintér, József Kovács, Rainer Haessner

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4 Citations (Scopus)


The reaction of an acetyl-protected symmetrical sugar carbodiimide with amines yielded the corresponding trisubstituted guanidine derivatives 2-6 with two or three sugar units. Their tautomerism, isomerism and conformational behaviour were elucidated by application of one- and two-dimensional 1H and 13C NMR spectroscopy. The rate of tautomerisation was calculated from ROESY exchange measurements.

Original languageEnglish
Pages (from-to)283-287
Number of pages5
JournalMagnetic Resonance in Chemistry
Issue number5
Publication statusPublished - Jan 1 2001



  • Conformational analysis
  • Exchange
  • Guanidino sugars
  • NMR
  • Tautomerism
  • c nmr
  • h nmr

ASJC Scopus subject areas

  • Chemistry(all)
  • Materials Science(all)

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