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• W2009546256 abstract "An enantioselective total synthesis of zampanolide has been accomplished using a novel DDQ/Brønsted acid promoted cyclization as the key reaction. The synthesis features cross-metathesis to construct the trisubstituted olefin and a ring-closing metathesis to form the macrolactone. The final N-acyl aminal formation was stereoselectively accomplished by an organocatalytic reaction." @default.
• W2009546256 created "2016-06-24" @default.
• W2009546256 creator A5031892138 @default.
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• W2009546256 date "2011-08-05" @default.
• W2009546256 modified "2023-09-26" @default.
• W2009546256 title "Enantioselective Total Synthesis of (−)-Zampanolide, a Potent Microtubule-Stabilizing Agent" @default.
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• W2009546256 doi "https://doi.org/10.1021/ol201626h" @default.
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