A concise synthetic approach to parvistemin A and (±)-diperezone

Literature Information

Publication Date 2017-04-27
DOI 10.1039/C7QO00216E
Impact Factor 5.281
Authors

Songsong Gao, Xiangdong Hu


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Abstract

A concise synthetic approach to symmetric biquinone skeletons has been developed through a new biomimetic oxidative phenolic coupling of 1,2,4-trihydroxyarenes using K3[Fe(CN)6] or FeCl3 as the oxidant under basic conditions. Merging with the ring expansion process of cyclobutenones, a synthetic strategy to biquinone natural products has been developed. And in the light of this strategy, total syntheses of parvistemin A and (±)-diperezone have been achieved.

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Organic Chemistry Frontiers

Organic Chemistry Frontiers
CiteScore: 7.8
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Organic Chemistry Frontiers publishes high-quality research from across organic chemistry. Emphases are placed on studies that make significant contributions to the field of organic chemistry by reporting either new or significantly improved protocols or methodologies. Topics include, but are not limited to the following: Organic synthesis Development of synthetic methodologies Catalysis Natural products Functional organic materials Supramolecular and macromolecular chemistry Physical and computational organic chemistry

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