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- W2021083363 abstract "The regioisomers of bis- and tris[C(6)-O-sulfonylated] α-cyclodextrins were converted in satisfactory yields to the corresponding C(6)-pyridinio derivatives, which afforded the characteristic splitting patterns of 1H NMR signals available for a regioisomer determination. Electrostatic repulsive interactions between the positively charged pyridinio groups play an important role in the remarkable splitting of the 1H NMR signals observed for some regioisomers." @default.
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- W2021083363 date "1988-10-01" @default.
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- W2021083363 title "1H NMR Study of the Regioisomers of PrimaryO-Di- and Trisubstituted α-Cyclodextrins" @default.
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- W2021083363 doi "https://doi.org/10.1246/bcsj.61.3409" @default.
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