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Miller, GJ and Gardiner, JM (2010) Adaptable Synthesis of C-Glycosidic Multivalent Carbohydrates and Succinamide-Linked Derivatization. Organic Letters, 12 (22). 5262 - 5265. ISSN 1523-7060
Full text not available from this repository.Abstract
A modular approach to the synthesis of trivalent C-glycosidic carbohydrates is described. The approach is illustrated employing carboxylate-terminated C-glycosidic d-mannose, d-glucose, and d-galactose derivatives with different length C1-linked spacer units and also core units with different length linker units attached. The central core scaffold is additionally functionalized via a succinamide-based, conjugatable linker unit, exemplified in an extended multivalent derivative [31] and a pyrene-bearing fluorsecent-labeled tris-C-mannosyl conjugate [33].
Item Type: | Article |
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Subjects: | Q Science > QD Chemistry |
Divisions: | Faculty of Natural Sciences > School of Physical and Geographical Sciences |
Related URLs: | |
Depositing User: | Symplectic |
Date Deposited: | 26 Nov 2015 10:48 |
Last Modified: | 12 Jun 2019 11:28 |
URI: | https://eprints.keele.ac.uk/id/eprint/1210 |