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- W2057261802 abstract "A biosynthetically inspired synthesis of (+)-liphagal has been achieved from (+)-sclareolide in 13 steps (9% overall yield). The key step is a biomimetic ring expansion of a highly stabilized benzylic carbocation, which generates the seven-membered ring and the benzofuran of the natural product in a single cascade reaction." @default.
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- W2057261802 date "2010-04-15" @default.
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- W2057261802 title "Enantiospecific, Biosynthetically Inspired Formal Total Synthesis of (+)-Liphagal" @default.
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- W2057261802 doi "https://doi.org/10.1021/ol100756z" @default.
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