𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Stereochemical studies by mass spectrometry: C15Nuphar alkaloids

✍ Scribed by O. Bortolini; G. Fantin; O. Curcuruto; P. Traldi; A. Iwanow; J. T. Wróbel


Publisher
John Wiley and Sons
Year
1991
Tongue
English
Weight
307 KB
Volume
26
Category
Article
ISSN
1076-5174

No coin nor oath required. For personal study only.

✦ Synopsis


Representative C,, Nuphar alkaloids, containing the quinolizidine system, were studied by high-resolution mass spectrometry and metastable-ion decomposition analysis. The appearance with N-oxide species of ions at m/z 168, useful in ascertaining the stereochemistry of the quinolizidinic ring junction, are ako discussed.


📜 SIMILAR VOLUMES


Stereochemical study of anagyrine-type q
✍ Zimin Liu; Li Yang; Zhongjian Jia; Jihong Chen 📂 Article 📅 1992 🏛 John Wiley and Sons 🌐 English ⚖ 224 KB

## Abstract The configurations of anagyrine, thermopsine and two other anagyrine‐type quinolizidine alkaloids were revised using ^15^N and 2D NMR in a 400 MHz NMR study. Their ^1^H and ^13^C NMR chemical shifts are given in detail.