Abstract
Novel 1-aza-6,11- and 1-aza-4,9-methnocyclopentacycloundecene ring systems were synthesized by the reaction of 3,8-methano[11]annulenone with N-(1-phenylvinylimino)triphenylphosphorane followed by dehydrogenation. These compounds are diatropic as 14pielectron vinylogues of 1-azaazulene.
| Original language | English |
|---|---|
| Pages (from-to) | 1291-1294 |
| Number of pages | 4 |
| Journal | Tetrahedron Letters |
| Volume | 31 |
| Issue number | 9 |
| DOIs | |
| Publication status | Published - 1990 |
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ASJC Scopus subject areas
- Biochemistry
- Drug Discovery
- Organic Chemistry
Cite this
Nitta, M., Kanomata, N., & Tada, M. (1990). Synthesis and spectroscopic properties of 1-azamkthanocyclopentacycloundecene ring systems. Tetrahedron Letters, 31(9), 1291-1294. https://doi.org/10.1016/S0040-4039(00)88788-2