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    Precursor 5 is then oxidized to 2-methyl- [1,4]benzoquinone (6). Finally, theobroxide (1) is 1 7 6 10 1802 Natural Product Communications Vol. 6 (12) 2011 Li et al. produced through epoxidization and reduction of both hydroxyl groups, and is converted to its carbonyldioxy derivative 2 by an unidentified mechanism.

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    Precursor 5 is then oxidized to 2-methyl- [1,4]benzoquinone (6). Finally, theobroxide (1) is 1 7 6 10 1802 Natural Product Communications Vol. 6 (12) 2011 Li et al. produced through epoxidization and reduction of both hydroxyl groups, and is converted to its carbonyldioxy derivative 2 by an unidentified mechanism.

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