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- W1566298733 abstract "A formal synthesis of the natural product (−)-flustramine B (3) is described, together with an easy and reliable approach for the absolute configuration assignment of a series of (3R,14S)- and (3S,14S)-oxindolylacetylphenyloxazolidinones 4, 6, 13a–c, and amides (+)- and (−)-14 by evaluation of the vibrational circular dichroism bisignated couplet resulting from the interaction of the C2 and C9 carbonyl groups. The absolute configuration assignment was validated by 1H NMR spectra and X-ray diffraction, and therefore (−)-flustramine B 3 was established as (3aS,8aR)-3." @default.
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- W1566298733 date "2015-07-01" @default.
- W1566298733 modified "2023-10-18" @default.
- W1566298733 title "Formal synthesis of (−)-flustramine B and its absolute configuration assignment by vibrational circular dichroism exciton chirality" @default.
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- W1566298733 doi "https://doi.org/10.1016/j.tetasy.2015.05.009" @default.
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