## Abstract For Abstract see ChemInform Abstract in Full Text.
Synthesis of isoindoloisoquinoline alkaloids. A revision of the structure of (±)-nuevamine
✍ Scribed by Ricardo Alonso; Luis Castedo; Domingo Domínguez
- Book ID
- 104229025
- Publisher
- Elsevier Science
- Year
- 1985
- Tongue
- French
- Weight
- 183 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
An easy and efficient method for the synthesis of isoindoloisoquinolines, and the assignment of a new structure for the alkaloid (k)-nuevamine are reported. (f)-Nuevamine lc is an alkaloid recently isolated from Berberis darwinii Hook, 1and is the first isoindoloisoquinoline reported from natural sources. The novelty of its skeleton prompted us to seek a synthetic route to this type of isoquinoline alkaloids. To this end a strategy was designed which rests upon the construction of the C-C bond linking the C-13 position with the aromatic ring A.
📜 SIMILAR VOLUMES
On the basis of chemical evidence and PMR spectral data the structure I (empirical formula C21H29NOs) was ascribed to clivorine 1 , an alkaloid isolated 2 from Ligdaria cZivorum
## Abstract The previous structure of the __Rauwolfia__ alkaloid raucaffricine (vomilenine‐α‐D‐galactoside) has been revised to be vomilenine‐β‐D‐Glucoside by enzymatic and NMR studies.