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Synthesis of the Tetracyclic ABCD Ring Systems of Madangamines D鈥揊
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文摘
Synthesis of the tetracyclic cores of madangamines D鈥揊 was achieved, featuring a reductive radical process from an ethoxycarbonyldichloroacetamide to build the morphan nucleus, a Mitsunobu-type aminocyclization toward the common diazatricyclic intermediate, and ring-closing metathesis reactions for the macrocyclization step leading to the 13- to 15-membered rings.

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