A synthesis of puraquinonic acid
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Soleiman Hisaindee; Derrick L.J Clive
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Article
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2001
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Elsevier Science
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French
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2-Methyl-1,4-benzenediol (10) was acylated with a-chloroisobutyroyl chloride and converted by treatment with AlCl 3 into the indanone derivative 12, which was elaborated into the substituted indane acid 24. Oxidation then afforded racemic puraquinonic acid.