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• W2078635296 abstract "A concise synthesis of the tricyclic core of the marine diterpene natural products labiatin A and australin A has been accomplished. The key ring-forming transformation is a cascade reaction comprising generation of a copper carbenoid from a diazo ketone, intramolecular reaction of the carbenoid with a cyclic ether, and rearrangement of the resulting free oxonium ylide or its metal-bound equivalent with ring expansion of the original cyclic ether." @default.
• W2078635296 created "2016-06-24" @default.
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• W2078635296 date "2011-07-06" @default.
• W2078635296 modified "2023-10-09" @default.
• W2078635296 title "Synthesis of the Tricyclic Core of Labiatin A and Australin A" @default.
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• W2078635296 doi "https://doi.org/10.1021/ol201498g" @default.
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