Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/4391
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Type: Journal article
Title: A versatile synthesis of linked cyclodextrins
Author: Easton, C.
van Eyk, S.
Lincoln, S.
May, B.
Papageorgiou, J.
Williams, M.
Citation: Australian Journal of Chemistry: an international journal for chemical science, 1997; 50(1):41883-
Publisher: C S I R O PUBLICATIONS
Issue Date: 1997
ISSN: 0004-9425
Statement of
Responsibility: 
Easton, Christopher J ; Eyk, Steven J. van ; Lincoln, Stephen F ; May, Bruce L ; Papageorgiou, John ; Williams, Michael L
Abstract: <jats:p> Reactions of amino-substituted cyclodextrins with bis(3-nitrophenyl) oxalate, malonate, succinate and glutarate, and with diphenyl carbonate, afford a range of linked cyclodextrins. These include α- and β-cyclodextrin dimers, joined by substitution at either C6 or C3, and asymmetric species with a β-cyclodextrin bonded to an a-cyclodextrin and a C3-substituted cyclodextrin attached to a C6-substituted moiety.</jats:p>
DOI: 10.1071/C96168
Published version: http://dx.doi.org/10.1071/c96168
Appears in Collections:Aurora harvest 2
Chemistry publications
Environment Institute publications

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