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• W2334689386 endingPage "4643" @default.
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• W2334689386 abstract "A novel synthetic path to sequosempervirin A was established by employing a samarium diiodide promoted intramolecular Barbier-type reaction of the lactonic iodide, in which the key structural feature, a spiro[4.5]decane ring system, could be constructed by controlling the stereochemistry of the hydroxyl group at the 8-position. The absolute configuration of natural sequosempervirin A was revised to be 4S based on this synthesis." @default.
• W2334689386 created "2016-06-24" @default.
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• W2334689386 date "2011-08-01" @default.
• W2334689386 modified "2023-10-07" @default.
• W2334689386 title "Integral Stereocontrolled Synthesis of a Spiro-norlignan, Sequosempervirin A: Revision of Absolute Configuration" @default.
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• W2334689386 doi "https://doi.org/10.1021/ol2018533" @default.
• W2334689386 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/21805972" @default.
• W2334689386 hasPublicationYear "2011" @default.
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