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- W2118959494 abstract "The key to successful coupling in the synthesis of (±)-quadrangularin A (1) was the introduction of tert-butyl groups in the precursor to block two reactive positions. Thus, the oxidative coupling of 3,5-di-(tert-butyl)resveratrol was carried out regioselectively in an efficient total synthesis of the natural product." @default.
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- W2118959494 date "2006-11-14" @default.
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- W2118959494 title "Total Synthesis of (±)-Quadrangularin A" @default.
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- W2118959494 doi "https://doi.org/10.1002/anie.200603097" @default.
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