Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/56310
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Type: Journal article
Title: Synthesis of C6A-to-C6A and C3A-to-C3A diamide linked γ-cyclodextrin dimers
Other Titles: Synthesis of C6A-to-C6A and C3A-to-C3A diamide linked gamma-cyclodextrin dimers
Author: Pham, D.T.
Ngo, H.
Lincoln, S.
May, B.
Easton, C.
Citation: Tetrahedron, 2010; 66(15):2895-2898
Publisher: Pergamon-Elsevier Science Ltd
Issue Date: 2010
ISSN: 0040-4020
Statement of
Responsibility: 
Duc-Truc Phama, Huy Tien Ngo, Stephen F. Lincoln, Bruce L. May and Christopher J. Easton
Abstract: The 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.
Keywords: Gamma-Cyclodextrin; Dimer; Synthesis
Rights: Copyright © 2010 Elsevier Ltd. All rights reserved
RMID: 0020095433
DOI: 10.1016/j.tet.2010.02.005
Appears in Collections:Chemistry publications
Environment Institute publications

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