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- W2951896065 abstract "A general stereocontrolled approach for entry into a family of highly biologically active 2,5-diaryl-3,4-disubstituted furano lignans has been developed. The key step involves a diastereoselective aldol-type condensation of an ester enolate having an α-chiral center with an aromatic aldehyde. The methodology has been illustrated with the total syntheses of (-)-talaumidin and (-)-virgatusin." @default.
- W2951896065 created "2019-06-27" @default.
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- W2951896065 date "2008-08-26" @default.
- W2951896065 modified "2023-09-25" @default.
- W2951896065 title "ChemInform Abstract: A Stereocontrolled Approach for the Synthesis of 2,5-Diaryl-3,4-disubstituted Furano Lignans Through a Highly Diastereoselective Aldol Condensation of an Ester Enolate with an α-Chiral Center: Total Syntheses of (-)-Talaumidin and (-)-Virgatusin." @default.
- W2951896065 cites W2117860604 @default.
- W2951896065 doi "https://doi.org/10.1002/chin.200835206" @default.
- W2951896065 hasPublicationYear "2008" @default.
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