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NMR spectroscopy: a powerful tool for detecting the conformational features of symmetrical persubstituted mixed cyclomaltoheptaoses (beta-cyclodextrins).

作者信息

Uccello-Barretta Gloria, Sicoli Giuseppe, Balzano Federica, Salvadori Piero

机构信息

Dipartimento di Chimica e Chimica Industriale, Università di Pisa, via Risorgimento 35, 56126 Pisa, Italy.

出版信息

Carbohydr Res. 2005 Feb 7;340(2):271-81. doi: 10.1016/j.carres.2004.11.022.

Abstract

The conformation in solution of exhaustively derivatized mixed cyclomaltooligosaccharides (cyclodextrins) has been defined by NMR spectroscopy. Both tilting of glucopyranose units about the glycosidic linkages and ring deviations from the 4C1 chair conformation are detected, the entities of which are strongly dependent on the nature of the derivatizing groups.

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