Synthesis of C6 A -to-C6 A and C3 A -to-C3 A diamide linked γ-cyclodextrin dimers

dc.contributor.authorPham, Duc-Truc
dc.contributor.authorNgo, Huy Tien
dc.contributor.authorLincoln, Stephen F
dc.contributor.authorMay, Bruce L
dc.contributor.authorEaston, Christopher
dc.date.accessioned2015-12-07T22:46:36Z
dc.date.issued2010
dc.date.updated2016-02-24T09:51:31Z
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-nitrophe
dc.identifier.issn0040-4020
dc.identifier.urihttp://hdl.handle.net/1885/25847
dc.publisherElsevier
dc.sourceTetrahedron
dc.subjectKeywords: 2 (4 nitrophenyl)succinate; amide; benzene derivative; carbon; carbon dioxide; diamide; dimer; gamma cyclodextrin derivative; glucopyranose; glucose derivative; n,n' 2 (3a deoxy gamma cyclodextrin 3a yl)succinamide; n,n' 2 (6a deoxy gamma cyclodextrin 6a Dimer; Gamma-cyclodextrin; Synthesis
dc.titleSynthesis of C6 A -to-C6 A and C3 A -to-C3 A diamide linked γ-cyclodextrin dimers
dc.typeJournal article
local.bibliographicCitation.issue15
local.bibliographicCitation.lastpage2898
local.bibliographicCitation.startpage2895
local.contributor.affiliationPham, Duc-Truc, University of Adelaide
local.contributor.affiliationNgo, Huy Tien, University of Adelaide
local.contributor.affiliationLincoln, Stephen F, University of Adelaide
local.contributor.affiliationMay, Bruce L, University of Adelaide
local.contributor.affiliationEaston, Christopher, College of Physical and Mathematical Sciences, ANU
local.contributor.authoremailu9500570@anu.edu.au
local.contributor.authoruidEaston, Christopher, u9500570
local.description.embargo2037-12-31
local.description.notesImported from ARIES
local.identifier.absfor030502 - Natural Products Chemistry
local.identifier.absseo970103 - Expanding Knowledge in the Chemical Sciences
local.identifier.ariespublicationu2544221xPUB41
local.identifier.citationvolume66
local.identifier.doi10.1016/j.tet.2010.02.005
local.identifier.scopusID2-s2.0-77949275170
local.identifier.thomsonID000276490800015
local.identifier.uidSubmittedByu2544221
local.type.statusPublished Version

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