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| | (6R,6aβ,13R,13aα)-Dodecahydro-6,13-methano-10H-pyrido[1,2-a]pyrrolo[1,2-e][1,5]diazocin-10-one Basic information |
| Product Name: | (6R,6aβ,13R,13aα)-Dodecahydro-6,13-methano-10H-pyrido[1,2-a]pyrrolo[1,2-e][1,5]diazocin-10-one | | Synonyms: | (-)-Camoensidine;(6R,6aβ,13R,13aα)-Dodecahydro-6,13-methano-10H-pyrido[1,2-a]pyrrolo[1,2-e][1,5]diazocin-10-one;Camoensidine;6,13-Methano-10H-pyrido[1,2-a]pyrrolo[1,2-e][1,5]diazocin-10-one, dodecahydro-, (6R,6aS,13R,13aR)- | | CAS: | 58845-84-4 | | MF: | C14H22N2O | | MW: | 234.34 | | EINECS: | | | Product Categories: | | | Mol File: | 58845-84-4.mol | ![(6R,6aβ,13R,13aα)-Dodecahydro-6,13-methano-10H-pyrido[1,2-a]pyrrolo[1,2-e][1,5]diazocin-10-one Structure](CAS/20180906/GIF/58845-84-4.gif) |
| | (6R,6aβ,13R,13aα)-Dodecahydro-6,13-methano-10H-pyrido[1,2-a]pyrrolo[1,2-e][1,5]diazocin-10-one Chemical Properties |
| | (6R,6aβ,13R,13aα)-Dodecahydro-6,13-methano-10H-pyrido[1,2-a]pyrrolo[1,2-e][1,5]diazocin-10-one Usage And Synthesis |
| Description | Camoensidine is one of two new alkaloids isolated with leontidine from Camoensia
maxima. The base has the fully reduced structure given which has been confirmed
by a partial synthesis from (±)-lupanine. | | References | Santamaria, Khuong Huu Laine, Phytochem., 14,2501 (1975) |
| | (6R,6aβ,13R,13aα)-Dodecahydro-6,13-methano-10H-pyrido[1,2-a]pyrrolo[1,2-e][1,5]diazocin-10-one Preparation Products And Raw materials |
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