Stereochemical investigations on ( E )‐homoeburnane derivatives by  1 H and  13 C NMR spectroscopy | Zendy

Tóth Gábor | Zendy; Szántay Csaba | Zendy; Kardos Zsuzsa | Zendy; Incze Mária | Zendy; Sóti Ferenc | Zendy; Kotovych George | Zendy

AI Assistant Blog Pricing

Home ZAIA Blog

Premium

Stereochemical investigations on ( E )‐homoeburnane derivatives by 1 H and 13 C NMR spectroscopy

Author(s) -

Tóth Gábor,

Szántay Csaba,

Kardos Zsuzsa,

Incze Mária,

Sóti Ferenc,

Kotovych George

Publication year - 1986

Publication title -

magnetic resonance in chemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.483

H-Index - 72

eISSN - 1097-458X

pISSN - 0749-1581

DOI - 10.1002/mrc.1260240811

Subject(s) - chemistry , diastereomer , carbon 13 nmr satellite , nuclear magnetic resonance spectroscopy , spectroscopy , proton , transverse relaxation optimized spectroscopy , two dimensional nuclear magnetic resonance spectroscopy , nuclear overhauser effect , nmr spectra database , fluorine 19 nmr , spectral line , proton nmr , decoupling (probability) , stereochemistry , crystallography , nuclear physics , physics , astronomy , engineering , quantum mechanics , control engineering

Several 14‐hydroxy‐14a‐methyl‐( E )‐homoeburnane diastereoisomers have been synthesized and studied by 1 H and 13 C NMR spectroscopy. ID NOE difference experiments, together with proton‐proton correlation and decoupling measurements, have allowed the complete assignment of the 1 H and 13 C NMR spectra. The relative configurations and predominant conformations have been established.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here

Accelerating Research