Structural elucidation of disubstituted nortricyclenes through vicinal 13C, 1H coupling constants

I. D. Gridnev, I. F. Leshcheva, N. M. Sergeyev, V. A. Chertkov

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10 Citations (Scopus)


Vicinal 13C, 1H coupling constants were used to establish the configuration of a 3,5‐disubstituted notricyclene. The assignment procedure is supported by independent measurements of 13C, 2H coupling constants in 3‐ deuterionortricyclene and confirmed by 1H, 1H NOE data for exo‐3‐N‐acetylamino‐exo‐5‐pivaloylnortricyclene.

Original languageEnglish
Pages (from-to)817-822
Number of pages6
JournalMagnetic Resonance in Chemistry
Issue number9
Publication statusPublished - 1992 Sep
Externally publishedYes


  • H coupling constants
  • Isotope effects
  • Vicinal C

ASJC Scopus subject areas

  • Chemistry(all)
  • Materials Science(all)

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