Affordable Access

Publisher Website

Nuclear magnetic resonance study of aporphine alkaloids—II:The structure of rogersine

Authors
Journal
Tetrahedron
0040-4020
Publisher
Elsevier
Publication Date
Volume
21
Issue
8
Identifiers
DOI: 10.1016/s0040-4020(01)98351-6

Abstract

Abstract The influence of alkali on the nuclear magnetic resonance spectra of some phenolic aporphine alkaloids has been studied. It is shown that shifts of the aromatic proton resonances greatly facilitate the elucidation of unknown structures in this series. The identity of rogersine and N-methyl-laurotetanine (II) has been established by this method.

There are no comments yet on this publication. Be the first to share your thoughts.