Article ID Journal Published Year Pages File Type
5280140 Tetrahedron Letters 2005 4 Pages PDF
Abstract
A new resveratrol tetramer, shoreaketone, was isolated from the stem bark of Shorea uliginosa (Dipterocarpaceae). The structure has a novel framework of heptacyclic ring system including an α,β-unsaturated carbonyl group. In NMR spectra shoreaketone is observed as two different conformers due to rotational isomerism.
Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry
Authors
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