| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5230192 | Tetrahedron | 2006 | 12 Pages |
Abstract
Seven new pentacyclic alkaloids sempervirine type have been synthesized via the AB-DE synthons obtainable by Fischer indolization of fused pyridines acetyl derivatives, which were formed in Diels-Alder reaction of 1,2,4-triazine precursor with cyclic enamines. New indolopyridocoline methoxy analogue has been obtained in the model synthesis from 2-acetylpyridine.
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Teodozja M. LipiÅska,
![First Page Preview: Total synthesis of new indolo[2,3-a]quinolizine alkaloids sempervirine type, potential pharmaceuticals Total synthesis of new indolo[2,3-a]quinolizine alkaloids sempervirine type, potential pharmaceuticals](/preview/png/5230192.png)