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- W2024496286 endingPage "S47" @default.
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- W2024496286 abstract "The properties of chiral spirochalcogenuranes acting as ligands in adducts with a chiral dirhodium tetracarboxylate complex is explored, and the individual adduct species are characterized by low-temperature NMR spectroscopy. Chiral recognition and the determination of enantiomeric composition of the chiral spirochalcogenuranes is easy by evaluating NMR signal dispersions both at low and at room- or slightly elevated temperatures. The uniformity in the signs of 1H dispersion effects and taking reference to the spiroselenurane with known absolute configuration [(S)-(–)-2] indicates that a convenient rule for the determination of absolute configuration in the spirochalcogenurane system can be established on the basis of 1H chemical shift dispersions. Chirality 17:S40–S47, 2005. © 2005 Wiley-Liss, Inc." @default.
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- W2024496286 date "2005-01-01" @default.
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- W2024496286 title "Effective enantiodifferentiation of spirochalcogenuranes by the dirhodium method: Towards the determination of absolute configurations?" @default.
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- W2024496286 doi "https://doi.org/10.1002/chir.20103" @default.
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