Gmelanone
 | |
| Names | |
|---|---|
| IUPAC name
(1R,2S,5S)-2,5-Bis(1,3-benzodioxol-5-yl)-3,6-dioxabicyclo[3.2.1]octan-8-one | |
| Identifiers | |
| 3D model (Jmol) | Interactive image |
| ChemSpider | 10308036 |
| |
| |
| Properties | |
| C20H16O7 | |
| Molar mass | 368.34 g·mol−1 |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Gmelanone is a lignan found in the heartwood of Gmelina arborea.[1] Arboreol can be transformed by acid catalysis into gmelanone.[2]
References
- ↑ Anjaneyulu, A.S.R.; Rao, A.Madhusudhana; Rao, V.Kameswara; Row, L.Ramachandra; Pelter, Andrew; Ward, Robert S. (1977). "Novel hydroxy lignans from the heartwood of gmelina arborea". Tetrahedron. 33: 133. doi:10.1016/0040-4020(77)80444-4.
- ↑ 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. doi:10.1016/S0040-4039(00)78645-X.
This article is issued from Wikipedia - version of the 11/28/2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.