| 词条 | Arboreol |
| 释义 |
| ImageFile = Arboreol acsv.svg | ImageSize = | IUPACName = (1R,4R,6aR)-1,4-Bis(1,3-benzodioxol-5-yl)dihydro-1H,3H-furo[3,4-c]furan-1,6a(6H)-diol | OtherNames = (7β,7'α,8α,8'α)-3,4:3',4'-bis(methylenedioxy)-7,9':7',9-diepoxylignane-7,8-diol |Section1={{Chembox Identifiers | CASNo_Ref = | CASNo = | ChemSpiderID = 16737548 | PubChem = 101277405 | KEGG_Ref = | KEGG = | ChEMBL_Ref = | ChEMBL = | SMILES = O[C@@]43CO[C@H](C4CO[C@]3(O)c1ccc2OCOc2c1)c5ccc6OCOc6c5 | InChI=1S/C20H18O8/c21-19-8-23-18(11-1-3-14-16(5-11)26-9-24-14)13(19)7-28-20(19,22)12-2-4-15-17(6-12)27-10-25-15/h1-6,13,18,21-22H,7-10H2/t13-,18-,19-,20+/m1/s1 | InChIKey = WQZHIPWFEKLEJM-AQWZQNETSA-N }} |Section2={{Chembox Properties | Formula = C20H18O8 | MolarMass = 386.35 g/mol | Appearance = | Density = | MeltingPt = | BoilingPt = | Solubility = |Section3={{Chembox Hazards | MainHazards = | FlashPt = | AutoignitionPt = }} Arboreol is an epoxylignan. Arboreol can be transformed by acid catalysis into gmelanone.[1] References1. ^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{{wiktionary}}{{lignan}}{{natural phenol-stub}} 3 : Lignans|Benzodioxoles|Chemical compounds found in |
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