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Studies directed toward the total synthesis of lancifodilactone G: An expeditious route to the ABC subunit

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卷 10, 期 11, 页码 2111-2113

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AMER CHEMICAL SOC
DOI: 10.1021/ol800418m

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An efficient entry to the ABC network of lancifodilactone G is outlined. The C ring is constructed by way of enyne ring-closing metathesis. The AB component is established via a base-mediated biomimetic oxy-Michael addition - lactonization sequence.

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