Arboreol
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| 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 | |
| ChemSpider | 16737548 |
| Jmol interactive 3D | Image |
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| Properties | |
| C20H18O8 | |
| Molar mass | 386.35 g/mol |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Arboreol is an epoxylignan.
Arboreol can be transformed by acid catalysis into gmelanone.[1]
References
- ↑ Acid catalysed rearrangements of arboreol: A biomimetic synthesis of gmelanone. L. Ramachandra Row and Reveru Ventkateswarlu, Tetrahedron Letters, 1980, Volume 21, Issue 30, Pages 2919–2922, doi:10.1016/S0040-4039(00)78645-X
External links
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Look up arboreol in Wiktionary, the free dictionary. |
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