The stereochemical features of per-O-acetyl-cyclomaltoheptaose (-b-cyclodextrin) have been investigated in solution by NMR spectroscopy, and the deviation of functionalised glucopyranose rings from 4C1 chairs to skew-type conformations has been detected.
A conformational model of per-O-acetyl-cyclomaltoheptaose(-b-cyclodextrin) in solution: detection of partial inversion of glucopyranose units by NMR spectroscopy
UCCELLO BARRETTA, GLORIA;BALZANO, FEDERICA;SALVADORI, PIERO
2003-01-01
Abstract
The stereochemical features of per-O-acetyl-cyclomaltoheptaose (-b-cyclodextrin) have been investigated in solution by NMR spectroscopy, and the deviation of functionalised glucopyranose rings from 4C1 chairs to skew-type conformations has been detected.File in questo prodotto:
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