【摘 要】
：
The first total synthesis of tubingensin A was finished starting from an advanced intermediate of anominine.The synthesis features a CuOTf-promoted 6π-electrocyclization/aromatization sequence to forg
【机 构】
：
State Key Laboratory of Bioorganic and Natural Products Chemistry,Shanghai Institute of Organic Chem
【出 处】
：
The 24th International Society of Heterocyclic Chemistry Con
论文部分内容阅读
The first total synthesis of tubingensin A was finished starting from an advanced intermediate of anominine.The synthesis features a CuOTf-promoted 6π-electrocyclization/aromatization sequence to forge the central region of the pentacyclic scaffold.
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