Lythranidine
Appearance
![]() | |
Names | |
---|---|
Systematic IUPAC name
(9S,11R,15R,17S)-23-Methoxy-25-azatetracyclo[18.3.1.12,6.111,15]hexacosa-1(24),2,4,6(26),20,22-hexaene-3,9,17-triol | |
Identifiers | |
3D model (JSmol)
|
|
1555440 | |
ChEBI | |
ChemSpider | |
PubChem CID
|
|
| |
| |
Properties | |
C26H35NO4 | |
Molar mass | 425.569 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|
Lythranidine is a piperidine alkaloid that was first isolated from the plant Lythrum anceps.[1] It contains a 17-membered cyclophane ring.
Several laboratory syntheses have been reported.[2][3][4][5]
References
[edit]- ^ Fujita, E; Fuji, K (1971). "Lythraceous alkaloids. Part IV. Structure and absolute configuration of lythranine, lythranidine, and lythramine". Journal of the Chemical Society C: Organic: 1651. doi:10.1039/J39710001651.
- ^ Fuji, Kaoru; Ichikawa, Kohei; Fujita, Eiichi (1980). "Lythraceous alkaloids. Part 11. Total synthesis of (±)-lythranidine". J. Chem. Soc., Perkin Trans. 1: 1066–1069. doi:10.1039/P19800001066.
- ^ Carruthers, William; Coggins, Peter; Weston, John B (1991). "Nitrone cycloaddition: An approach to the cyclophane alkaloid (±)-lythranidine". J. Chem. Soc., Perkin Trans. 1 (3): 611–616. doi:10.1039/P19910000611.
- ^ Pinder, A. R (1992). "Azetidine, pyrrole, pyrrolidine, piperidine, and pyridine alkaloids". Natural Product Reports. 9 (5): 491. doi:10.1039/NP9920900491.
- ^ Gebauer, Konrad; Fürstner, Alois (2014). "Total Synthesis of the Biphenyl Alkaloid (−)-Lythranidine" (PDF). Angewandte Chemie International Edition. 53 (25): 6393–6396. doi:10.1002/anie.201402550. PMID 24821137.