hongoquercin-a has been researched along with sclareol* in 1 studies
1 other study(ies) available for hongoquercin-a and sclareol
Article | Year |
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A short synthetic route towards merosesquiterpenes with a benzoxanthene skeleton.
A short synthetic sequence for the preparation of merosesquiterpenes with a benzoxanthene skeleton starting from commercial (-)-sclareol is reported. The D ring of the target compound is obtained through a Diels-Alder cycloaddition, involving a dienoldiether derived from a tricyclic α,β-enone synthesized in two steps from the starting diterpene. Utilizing this procedure, the preparation of (+)-hongoquercin A and the first synthesis of (+)-cyclospongiaquinone-1 were achieved. Topics: Antineoplastic Agents; Cycloaddition Reaction; Diterpenes; Sesquiterpenes; Stereoisomerism; Xanthenes | 2014 |