Konstitution und Reaktionen des (+)-Pronuciferins 3. Mitteilung über natürliche und synthetische Isochinolinderivate
✍ Scribed by Karl Bernauer
- Publisher
- John Wiley and Sons
- Year
- 1964
- Tongue
- German
- Weight
- 508 KB
- Volume
- 47
- Category
- Article
- ISSN
- 0018-019X
No coin nor oath required. For personal study only.
✦ Synopsis
First isolation of the isoquinolinedienone alkaloid Pronuciferine (I), and of the noraporphine alkaloid Anonaine (V), besides the aporphines Nuciferine (11) , Roemerine (III), and 5-Methoxy-6-hydroxy-aporphine (IV), from cotyledons of Nelzlmbo nucifeera GAERTN. (Asiatic Lotus) is described.
📜 SIMILAR VOLUMES
Bespriihen der PIatten rnit Kaliumjodoplatinat-Losung sichtbar gemacht. 6 , Aus Hongkong bezogen. 7) TOMITA u. Mitarb. [3] geben fur Nornuciferin den Smp. 195-196" und [ w ] g = -265" (c = 0,506. Chloroform) an.
## Abstract Synthesis and cardiovascular evaluation of ketones **10**, **11** and **12** and of their derivatives **14** to **35** are described.
## 1583 The results of the X-ray analysis of 1,1,5,5-tetramethylcyclodecane-8-carboxylic acid do not correspond to a reasonable molecular structure. When used as a startingpoint for a strain-energy minimization calculation based on semi-empirical potential functions, they lead to two new contormat
\4 1 2 3 a) Die Verbindungen 7-9 und 15-17 konnten nicht in kristallisierter Form gefasst werden. 8-10, 15 und 16 stellen hochstwahrscheinlich Diastereomerengemische dar.