Determination of the configuration of substituted 1,4

3,6‐dianhydrohexitols by 13C NMR spectroscopy

P. Sohár, G. Medgyes, J. Kuszmann

Research output: Contribution to journalArticle

9 Citations (Scopus)

Abstract

The configurations of 1,4:3,6‐dianhydro‐2,5‐di‐O‐mesyl‐D‐mannitol, 1,4:3,6‐dianhydro‐2,5‐di‐O‐mesyl‐D‐glucitol, 1,4:3,6‐dianhydro‐2,5‐di‐O‐mesyl‐L‐iditol, 1,4:3:6‐dianhtydro‐2‐deoxy‐2‐iodo‐5‐O‐mesyl‐D‐mannitol, 1,4:3:6‐dianhtydro‐2‐deoxy‐2‐iodo‐5‐O‐mesyl‐D‐glucitol, 1,4:3,6‐dianhydro‐2‐deoxy‐2‐iodo‐5‐O‐mesyl‐L‐iditol, 1,4:3,6‐dianhydro‐2,5‐dideoxy‐2,5‐diiodo‐D‐glucitol and 1,4:3,6‐dianhydro‐2,5‐dideoxy‐2,5‐diiodo‐L‐iditol were determined by 13C NMR spectroscopy, by invoking the field‐effect.

Original languageEnglish
Pages (from-to)357-359
Number of pages3
JournalOrganic Magnetic Resonance
Volume11
Issue number7
DOIs
Publication statusPublished - 1978

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Nuclear magnetic resonance spectroscopy

ASJC Scopus subject areas

  • Chemistry(all)
  • Materials Science(all)

Cite this

Determination of the configuration of substituted 1,4 : 3,6‐dianhydrohexitols by 13C NMR spectroscopy. / Sohár, P.; Medgyes, G.; Kuszmann, J.

In: Organic Magnetic Resonance, Vol. 11, No. 7, 1978, p. 357-359.

Research output: Contribution to journalArticle

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abstract = "The configurations of 1,4:3,6‐dianhydro‐2,5‐di‐O‐mesyl‐D‐mannitol, 1,4:3,6‐dianhydro‐2,5‐di‐O‐mesyl‐D‐glucitol, 1,4:3,6‐dianhydro‐2,5‐di‐O‐mesyl‐L‐iditol, 1,4:3:6‐dianhtydro‐2‐deoxy‐2‐iodo‐5‐O‐mesyl‐D‐mannitol, 1,4:3:6‐dianhtydro‐2‐deoxy‐2‐iodo‐5‐O‐mesyl‐D‐glucitol, 1,4:3,6‐dianhydro‐2‐deoxy‐2‐iodo‐5‐O‐mesyl‐L‐iditol, 1,4:3,6‐dianhydro‐2,5‐dideoxy‐2,5‐diiodo‐D‐glucitol and 1,4:3,6‐dianhydro‐2,5‐dideoxy‐2,5‐diiodo‐L‐iditol were determined by 13C NMR spectroscopy, by invoking the field‐effect.",
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