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本文引用的文献
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Stereochemically versatile synthesis of the C1-C12 fragment of tedanolide C.
Org Lett. 2012 Mar 16;14(6):1452-5. doi: 10.1021/ol300194x. Epub 2012 Feb 29.
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A Kiyooka aldol approach for the synthesis of the C(14)-C(23) segment of the diastereomeric analog of tedanolide C.
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New candidaspongiolides, tedanolide analogues that selectively inhibit melanoma cell growth.
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Total synthesis of plakortide E and biomimetic synthesis of plakortone B.
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Enantioselective synthesis of alpha-methylene-beta-hydroxy carboxylic acid derivatives via a diastereoselective aldol/beta-elimination sequence: application to the C(15)-C(21) fragment of tedanolide C.
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The asymmetric total synthesis of (+)-cytotrienin a, an ansamycin-type anticancer drug.
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Inside cover: total synthesis and configurational assignment of pasteurestin a and B (Angew. Chem. Int. Ed. 48/2007).
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Mosher ester analysis for the determination of absolute configuration of stereogenic (chiral) carbinol carbons.
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Candidaspongiolides, distinctive analogues of tedanolide from sponges of the genus Candidaspongia.
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Tedanolide C: a potent new 18-membered-ring cytotoxic macrolide isolated from the Papua New Guinea marine sponge Ircinia sp.
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