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• W2320565661 startingPage "4134" @default.
• W2320565661 abstract "The tetracyclic core of daphniglaucin C was prepared from the known 4-keto-N-Boc methyl-l-prolinate in 15 steps with a cumulative yield of 14.7%. The key steps toward this core motif feature a reductive double bond transposition from an unactivated tertiary allylic alcohol, a Pd-catalyzed Stille coupling, and Dieckmann cyclizations." @default.
• W2320565661 created "2016-06-24" @default.
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• W2320565661 date "2013-07-26" @default.
• W2320565661 modified "2023-10-03" @default.
• W2320565661 title "Concise and Stereocontrolled Synthesis of the Tetracyclic Core of Daphniglaucin C" @default.
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• W2320565661 doi "https://doi.org/10.1021/ol4018112" @default.
• W2320565661 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/23889206" @default.
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