Natural Abundance Nitrogen-15 NMR: A Study About the Conformation and Protonation Site of Some Quinoline Alkaloids
作者:
J. Schripsema,
R. Verpoorte,
A.Baerheim Svendsen,
C. Erkelens,
期刊:
Spectroscopy Letters
(Taylor Available online 1987)
卷期:
Volume 20,
issue 10
页码: 777-783
ISSN:0038-7010
年代: 1987
DOI:10.1080/00387018708081586
出版商: Taylor & Francis Group
关键词: 15N-NMR;quinoline alkaloids.
数据来源: Taylor
摘要:
Natural abundance15N-NMR spectra were obtained from quinidine, quinine and epiquinidine. Correlation of the15N chemical shifts with X-ray studies and minimal energy conformer calculations, reported previously, enabled definite conclusions about the solution conformations of these alkaloids. Also the protonation of quinidine in CDCl3was studied. It was determined that the first protonation occurs on the quinuclidine nitrogen and not on the quinoline nitrogen as was reported by Yanuka et al.1
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