Abstract
In search of new lead structures for potent allosteric enhancers of antagonist binding to muscarinic M2 receptors, a novel heterocyclic ring system, 6,7,14,15-tetrahydro-15aH-azocino[1,2-a:6,5-b′]diindole, has been synthesized. The new ring skeleton was obtained from indol-2-yl-acetic acid in three steps.
| Original language | English |
|---|---|
| Pages (from-to) | 7183-7186 |
| Number of pages | 4 |
| Journal | Tetrahedron Letters |
| Volume | 44 |
| Issue number | 38 |
| DOIs | |
| Publication status | Published - 15 Sept 2003 |
| Externally published | Yes |
Keywords
- 6,7,14,15-tetrahydro-15aH-azocino[1,2-a:6,5-b′]diindole
- Dimerization of 2-(indol-2-yl)-ethyl tosylate
- Ligands for the allosteric binding site of muscarinic M2 receptors
- Novel pentacyclic ring system
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