z-logo
Premium
An NMR study of spatial arrangements in natural alkaloids—I: Indor spectra and conformations of pachycarpine ( d ‐sparteine), lupanine and 13‐hydroxylupanine
Author(s) -
Sadykov A. S.,
Kamayev F. G.,
Korenevsky V. A.,
Leon'ev V. B.,
Ustynyuk Yu. A.
Publication year - 1972
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.1270040608
Subject(s) - sparteine , quinolizidine , homonuclear molecule , stereochemistry , chemistry , nmr spectra database , spectral line , alkaloid , physics , molecule , organic chemistry , astronomy
The INDOR homonuclear PMR spectra of three quinolizidine alkaloids—pachycarpine ( d ‐sparteine), lupanine and 13‐hydroxylupanine—have been studied. The molecular conformations including the boat‐structure of the ring C have been established.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom