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A hitherto undetected phenolic fraction in Anacardium occidentale(in the nut-shell liquid and not in the edible kernel) has been shown spectroscopically and chromatographically to comprise the saturated phenol 2-methyl-5-pentadecylresorcinol, its 2-methyl-5-[(8Z)-pentadec-8-enyl], 2-methyl-5-[(8Z,11Z)-pentadeca-8,11-dienyl], and 2-methyl-5-[(8Z,11Z)-pentadeca-8,11,14-trienyl] analogues, and small amounts of C17 components. The unsaturated members are converted by hydrogenation of the side-chain into the saturated phenol, which has been synthesised. The 4-methyl analogue is absent and occurrence of the novel phenol is an instance of specific C-methylation. We report C-demethylation and isomer formation during the syntheses of the 2- and the 4-methyl saturated phenols.
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John H. P. Tyman (1973) studied this question.
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