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• W2133715622 endingPage "868" @default.
• W2133715622 startingPage "865" @default.
• W2133715622 abstract "Abstract An efficient synthetic route toward the highly congested [5‐6‐7] tricyclic core of calyciphylline A‐type alkaloids has been developed. This approach features a highly efficient intramolecular Diels–Alder cycloaddition to establish the aza‐five‐membered C ring as well as the C1 all‐carbon quaternary center, and a subsequent cyclopropanation together with a ring‐expansion reaction of the resulted adduct to construct the seven‐membered D ring." @default.
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• W2133715622 date "2014-11-05" @default.
• W2133715622 modified "2023-10-07" @default.
• W2133715622 title "Expedient Construction of the [5-6-7] Tricyclic Core of Calyciphylline A-Type Alkaloids" @default.
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• W2133715622 doi "https://doi.org/10.1002/asia.201403061" @default.
• W2133715622 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/25377776" @default.
• W2133715622 hasPublicationYear "2014" @default.
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