Publication | Closed Access
Total Synthesis of Propolisbenzofuran B
11
Citations
69
References
2017
Year
Medicinal ChemistryBioorganic ChemistryAlkene MetathesisNatural SciencesPropolisbenzofuran BOrganic ChemistryEfficient SynthesisChemistryHeterocycle ChemistryKey Cyclohexanone FrameworkPharmacologySynthetic ChemistryNatural Product Synthesis
An efficient synthesis of propolisbenzofuran B, which possesses promising anticancer activity, is reported. The key cyclohexanone framework of this tricyclic natural product has been constructed employing a Rh-catalyzed intramolecular olefin hydroacylation. The requisite key olefin intermediate was synthesized by using gold-catalyzed allenyl ether [1,3] O → C rearrangement.
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