Title of article
A conformational model of per-O-acetyl-cyclomaltoheptaose (-β-cyclodextrin) in solution: detection of partial inversion of glucopyranose units by NMR spectroscopy Original Research Article
Author/Authors
Gloria Uccello Barretta، نويسنده , , Giuseppe Sicoli، نويسنده , , Federica Balzano، نويسنده , , Piero Salvadori، نويسنده ,
Issue Information
دوهفته نامه با شماره پیاپی سال 2003
Pages
5
From page
1103
To page
1107
Abstract
The stereochemical features of per-O-acetyl-cyclomaltoheptaose (-β-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.
Keywords
Cyclomaltooligosaccharides , Cyclodextrins , NMR , Stereochemistry , Conformational distortions
Journal title
Carbohydrate Research
Serial Year
2003
Journal title
Carbohydrate Research
Record number
963741
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