Four-Step Total Synthesis of Selaginpulvilin D
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Sherburn, Michael
Sowden, Madison
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American Chemical Society
Abstract
An extremely concise total synthesis of a potent phosphodiesterase-4 inhibitory natural product, selaginpulvilin D, is reported. The synthesis features a one-pot, 3-fold electrophilic aromatic substitution sequence to assemble a 9,9-diarylfluorene core. The approach allows access to useful quantities of a selaginpulvilin natural product for the first time.
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Organic Letters
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Restricted until
2037-12-31