## Abstract For Abstract see ChemInform Abstract in Full Text.
Synthesis of a new conformationally defined serotonin homologue by intramolecular [4+2] cycloaddition
✍ Scribed by M. Herslöf; A.R. Martin*
- Publisher
- Elsevier Science
- Year
- 1987
- Tongue
- French
- Weight
- 219 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0040-4039
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📜 SIMILAR VOLUMES
A novel one-step construction of bicyclo[5.3.l]undecane skeleton via intramolecular cycloaddition of allenyl ethers is described.
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Thermolysis of the 1-v-azidoalkylindoles 4, bearing an electron attracting substituent at C-3 (CHO, COMe, COOMe, CN) provides imidazo[1,2-a]indoles (5, n=1), pyrimidino[1,2-a]indoles (5, n=2), and 1,3-diazepino[1,2-a]indoles (5, n=3).