A Biomimetic Strategy for the Synthesis of the Tricyclic Dibenzofuran-1,4-dione Core of Popolohuanone E
Author:
Affiliation:
1. School of Chemistry, University of Nottingham, Nottingham NG7 2RD, U.K.
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol047825o
Reference21 articles.
1. Popolohuanone E, a topoisomerase-II inhibitor with selective lung tumor cytotoxicity from the Pohnpei sponge Dysidea sp.
2. Arenarol and arenarone: sesquiterpenoids with rearranged drimane skeletons from the marine sponge Dysidea arenaria
3. Studies toward the synthesis of popolohuanone E: Synthesis of natural (+)-arenarol related to the proposed biogenetic precursor of popolohuanone E
4. Synthesis of various model compounds for the central tricyclic ring system of popolophuanone E
5. Application of the Nickel-Mediated Neopentyl Coupling in the Total Synthesis of the Marine Natural Product Arenarol
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