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- W2951027085 abstract "[reaction: see text] The trimeric quinone framework of conocurvone is crucial for its potent anti-HIV activity. A new synthesis of trimeric quinones based on stepwise substitution of the halogens in 2,3-dihaloquinones by hydroxyquinone anions is described. Chlorinated biquinones are key intermediates that undergo regiospecific substitution reactions to yield trimeric quinone monomethyl ethers." @default.
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- W2951027085 date "2002-01-22" @default.
- W2951027085 modified "2023-09-24" @default.
- W2951027085 title "Regiocontrolled Synthesis of the Trimeric Quinone Framework of Conocurvone" @default.
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- W2951027085 doi "https://doi.org/10.1021/ol010272m" @default.
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