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dc.contributor.authorPham, D.en
dc.contributor.authorNgo, H.en
dc.contributor.authorLincoln, S.en
dc.contributor.authorMay, B.en
dc.contributor.authorEaston, C.en
dc.identifier.citationTetrahedron, 2010; 66(15):2895-2898en
dc.description.abstractThe syntheses of three new diamide-linked γ-cyclodextrin dimers joined by substitution at either a glucopyranose C6A or C3A carbon are reported. The syntheses involve the reaction of either C6A or C3A amino-substituted γ-cyclodextrin with bis(4-nitrophenyl)succinate to form succinamide linked γ-cyclodextrin dimers or reaction of C6A azide-substituted γ-cyclodextrin with carbon dioxide to form a urea linked γ-cyclodextrin dimer.en
dc.description.statementofresponsibilityDuc-Truc Phama, Huy Tien Ngo, Stephen F. Lincoln, Bruce L. May and Christopher J. Eastonen
dc.publisherPergamon-Elsevier Science Ltden
dc.rightsCopyright © 2010 Elsevier Ltd. All rights reserveden
dc.subjectGamma-Cyclodextrin; Dimer; Synthesisen
dc.titleSynthesis of C6A-to-C6A and C3A-to-C3A diamide linked γ-cyclodextrin dimersen
dc.title.alternativeSynthesis of C6A-to-C6A and C3A-to-C3A diamide linked gamma-cyclodextrin dimersen
dc.typeJournal articleen
pubs.library.collectionChemistry publicationsen
dc.identifier.orcidPham, D. [0000-0001-9383-6699]en
Appears in Collections:Chemistry publications
Environment Institute publications

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