Author:
Batterham TJ,Bell KH,Weiss U
Abstract
The nuclear magnetic resonance spectra of
codeine, isocodeine, pseudocodeine, allopseudocodeine, neopine, isoneopine, and
some of their derivatives have been studied and the patterns produced by the
protons on dl rings except the N-heterocyclic ring have been analysed by
first-order methods. Allylic, homoallylic, and other long-range couplings have
been observed. Differences in chemical shift between protons in different
isomers have been explained in terms of the anisotropy of the double bond or
the aromatic ring.
Cited by
49 articles.
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