| |
| Names | |
|---|---|
| IUPAC name
(1R,4R,6aR)-1,4-Bis(1,3-benzodioxol-5-yl)dihydro-1H,3H-furo[3,4-c]furan-1,6a(6H)-diol
| |
| Other names
(7β,7'α,8α,8'α)-3,4:3',4'-bis(methylenedioxy)-7,9':7',9-diepoxylignane-7,8-diol
| |
| Identifiers | |
3D model (JSmol)
|
|
| ChemSpider | |
PubChem CID
|
|
| |
| |
| Properties | |
| C20H18O8 | |
| Molar mass | 386.356 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
| |
Arboreol is an epoxylignan. Arboreol can be transformed by acid catalysis into gmelanone.[2]
References
- ^ Buckingham, John (2 December 1993). Dictionary of Natural Products. CRC Press. p. 481. ISBN 978-0-412-46620-5.
- ^ Ramachandra Row, L.; Ventkateswarlu, Reveru; Pelter, Andrew; Ward, Robert S. (1980). "Acid catalysed rearrangements of arboreol: A biomimetic synthesis of gmelanone". Tetrahedron Letters. 21 (30): 2919–2922. doi:10.1016/S0040-4039(00)78645-X.
External links
The dictionary definition of arboreol at Wiktionary
 | This article about an aromatic compound is a stub. You can help Wikipedia by expanding it. |
This page was last edited on 11 March 2024, at 17:36