A versatile synthesis of linked cyclodextrins
Date
1997
Authors
Easton, C.
van Eyk, S.
Lincoln, S.
May, B.
Papageorgiou, J.
Williams, M.
Editors
Advisors
Journal Title
Journal ISSN
Volume Title
Type:
Journal article
Citation
Australian Journal of Chemistry, 1997; 50(1):41883-
Statement of Responsibility
Easton, Christopher J ; Eyk, Steven J. van ; Lincoln, Stephen F ; May, Bruce L ; Papageorgiou, John ; Williams, Michael L
Conference Name
DOI
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 a- and ß-cyclodextrin dimers, joined by substitution at either C6 or C3, and asymmetric species with a ß-cyclodextrin bonded to an a-cyclodextrin and a C3-substituted cyclodextrin attached to a C6-substituted moiety.</jats:p>