Saturated 5‐membered ring conformation. 1— 1 H NMR study of protonated methyltetrahydrofurans in superacid medium | Zendy

Infarnet Y. | Zendy; Duplan J. C. | Zendy; Huet J. | Zendy

AI Assistant Blog Pricing

Home ZAIA Blog

Premium

Saturated 5‐membered ring conformation. 1— 1 H NMR study of protonated methyltetrahydrofurans in superacid medium

Author(s) -

Infarnet Y.,

Duplan J. C.,

Huet J.

Publication year - 1981

Publication title -

organic magnetic resonance

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.483

H-Index - 72

eISSN - 1097-458X

pISSN - 0030-4921

DOI - 10.1002/mrc.1270160119

Subject(s) - protonation , superacid , ring (chemistry) , chemistry , coupling constant , proton nmr , oxygen , crystallography , computational chemistry , stereochemistry , organic chemistry , physics , ion , catalysis , particle physics

Several methyltetrahydrofurans have been studied in HSO 3 FSbF 5 SO 2 solution. O ‐Protonation was observed from 1 H NMR measurements at low temperature, and the coupling constants between + OH and the CH protons α to oxygen were measured from the CH signals. A conformational interpretation could be carried out from these results.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here

Accelerating Research