Tools
Tools
Garcı́a-Aparicio, Vı́ctor, Fernández-Alonso, Marı́a Del Carmen, Angulo, Jesús 
ORCID: https://orcid.org/0000-0001-7250-5639, Asensio, Juan Luis, Cañada, Fco. Javier, Jiménez-Barbero, Jesús, Mootoo, David R. and Cheng, Xuhong
(2005)
The conformational behaviour of α,β-trehalose-like disaccharides and their C-glycosyl, imino-C-glycosyl and carbagalactose analogues depends on the chemical nature of the modification: an NMR investigation.
Tetrahedron: Asymmetry, 16 (2).
pp. 519-527.
ISSN 0957-4166
Abstract
The conformational behaviour of ß-O-Gal-(1?1)-a-Man 4 and the C-glycoside, carbaglycoside and aza-C-glycoside mimics 1–3 has been studied using J/NOE NMR data, molecular mechanics and molecular dynamics. It is shown that the population distributions around the glycosidic linkages of the different analogues depend on the chemical nature of the acetal or pseudoacetal residue.
| Item Type: | Article |
|---|---|
| Faculty \ School: | Faculty of Science > School of Pharmacy |
| Depositing User: | Pure Connector |
| Date Deposited: | 21 Oct 2013 19:36 |
| Last Modified: | 24 Oct 2022 04:49 |
| URI: | https://ueaeprints.uea.ac.uk/id/eprint/43765 |
| DOI: | 10.1016/j.tetasy.2004.11.072 |
Actions (login required)
 |
View Item |