【摘 要】
：
The common tricyclic intermediate of calyciphylline A subfamily daphniphyllum alkaloid was constructed by a gold-catalyzed 6-exo-dig alkyne-cyclization reaction[1] and a subsequent intramolecular Mich
【机 构】
：
State Key Laboratory of Bioorganic and Natural Products Chemistry,Shanghai Institute of Organic Chem
【出 处】
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The 24th International Society of Heterocyclic Chemistry Con
论文部分内容阅读
The common tricyclic intermediate of calyciphylline A subfamily daphniphyllum alkaloid was constructed by a gold-catalyzed 6-exo-dig alkyne-cyclization reaction[1] and a subsequent intramolecular Michael addition reaction.
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