Several 7a-substituted benzoylaminoalkyl-hexahydro-1 H-pyrrolizines were synthesized by acylations of 7a-aminoalkyl-hexahydro-1 H-pyrrolizines. All compounds synthesized were evaluated for their antiarrhythmic activities using the chloroform-mouse method, and some of them were found to have signific
Some chemical transformations of 7a-cyanohexahydro-1H-pyrrolizine into 7a-substituted hexahydro-1H-pyrrolizines
β Scribed by Seiji Miyano; Osamu Yamashita; Kunihiro Sumoto; Keiyu Shima; Mariko Hayashimatsu; Fumio Satoh
- Book ID
- 112128463
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 1987
- Tongue
- English
- Weight
- 228 KB
- Volume
- 24
- Category
- Article
- ISSN
- 0022-152X
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Synthesis of (1R,2R,3R,7R,7aR)-Hexahydro-3-(hydroxymethyl)-1Hpyrrolizine-1,2,7-triol: 7-Epiaustraline. -Title compound (VI) is synthesized from known nitronate (I), prepared via [4 + 2] cycloaddition, in order to establish [4 + 2]/[3 + 2] cycloaddition chemistry as a general strategy for the synthe
Single-crystal X-ray study T = 200 K Mean '(CΒ±C) = 0.003 A Γ R factor = 0.032 wR factor = 0.081 Data-to-parameter ratio = 9.4 For details of how these key indicators were automatically derived from the article, see http://journals.iucr.org/e.