Studies Directed toward the Total Synthesis of Lancifodilactone G: An Expeditious Route to the ABC Subunit.

[摘要]：An efficient entry to the ABC network I of lancifodilactone G is outlined. The C ring is constructed by way of enyne ring-closing metathesis of II. The AB component is established via a base-mediated biomimetic oxy-Michael addn.-lactonization sequence of cycloheptane diol III.

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