Abstract
In search of new lead structures for potent allosteric enhancers of antagonist binding to muscarinic M2 receptors, the first representative of a novel heterocyclic ring system, 6,7,14,15-tetrahydro[1,5]diazocino[1,2-a:6,5-a′]diindole, has been synthesized. The new pentacyclic ring skeleton is obtained from [3-(2-dibenzylaminoethyl)indol-2-yl]-acetic acid methyl ester in three steps.
| Original language | English |
|---|---|
| Pages (from-to) | 391-394 |
| Number of pages | 4 |
| Journal | Tetrahedron |
| Volume | 59 |
| Issue number | 3 |
| DOIs | |
| Publication status | Published - 13 Jan 2003 |
| Externally published | Yes |
Keywords
- 6,7,14,15-tetrahydro[1,5]diazocino[1,2-a:6,5-a′]diindole
- Dimerization of bromoethylindole
- Muscarinic active compounds
- Novel pentacyclic ring system
Fingerprint
Dive into the research topics of '6,7,14,15-Tetrahydro[1,5]diazocino[1,2-a:6,5-a′]diindole. Synthesis of a novel pentacyclic ring system'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver