期刊
ORGANIC LETTERS
卷 12, 期 4, 页码 780-783出版社
AMER CHEMICAL SOC
DOI: 10.1021/ol902848k
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资金
- California Institute of Technology
Preparation of the polycyclic core of the cytotoxic natural product salvileucalin B is described. The key feature of this synthetic strategy is a copper-catalyzed intramolecular arene cyclopropanation to provide the central norcaradiene. These studies lay the foundation for continued investigations toward an enantioselective total synthesis of 1.
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