Photochemical synthesis of isoindolo[1,2-b] [3]benzazepine derivatives. Preparation of schőpf-schweickert amine VI
✍ Scribed by Heinz O. Bernhard; Victor Snieckus
- Book ID
- 104248438
- Publisher
- Elsevier Science
- Year
- 1971
- Tongue
- French
- Weight
- 225 KB
- Volume
- 12
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
In 1965, outstanding efforts by ?5anta$ and coworkers culminated in the structural elucidation of rhoeadine (la) which proved to be the first member of the significant and biosynthetically intriguing 3 Rhoeadine group of alkaloids belonging to the benzylisoquinoline 4 family . Until recently, the state of the synthetic art in this area appeared to lie in dormancy. In view of the abrupt awakening of interest 5,6,7 , we wish to report our different approach 8 to this group of alkaloids which involves a new and apparently general type of
📜 SIMILAR VOLUMES
pyridines have been prepared from 7-azaindole by lithiation followed by addition of various electrophiles. A 7-azaolivacine analogue and a pyrido[3'2':4,5]pyrrolo[ 1,2-c]pyrido [3,2-d]pyrimidine have also been prepared.