Carbon-13 Nuclear Magnetic Resonance Study of meso-Hexestrol and Its Derivatives

Taiko Oda, Tomoko Murai, Yoshihiro Sato

Research output: Contribution to journalArticlepeer-review

9 Citations (Scopus)


The carbon-13 nuclear magnetic resonance chemical shift assignments for meso-hexestrol (la), made on the basis of two-dimensional 13C-1H chemical shift correlation, long-range selective 1H decoupling experiment, and a reported two-dimensional Fourier-transform experiment for long-range proton-carbon-13 spin coupling constants, are reported. For measurement of carbon-proton coupling constants of meso-hexestrol derivatives (lb—e, 2a—d, 3a—c, and 4), the coupling information was detected by using a gated decoupling facility which permitted retention of the nuclear Overhauser enhancement and a long-range selective 1H decoupling experiment. The results showed that the aromatic carbon resonances are influenced by the structure (no double bond, or one or two double bond(s)) of the hexane framework in the central portion.

Original languageEnglish
Pages (from-to)1534-1539
Number of pages6
JournalChemical and Pharmaceutical Bulletin
Issue number4
Publication statusPublished - 1988 Jan 1


  • 13C-NMR
  • 1H-NMR meso-hexestrol
  • dienestrol
  • diethylstilbestrol
  • hexestrol derivative
  • isodienestrol

ASJC Scopus subject areas

  • General Chemistry
  • Drug Discovery


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