A cyclodextrin molecular reactor for the regioselective synthesis of 1,5-disubstituted-1,2,3-triazoles

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dc.contributor.authorBarr, Lorna
dc.contributor.authorLincoln, Stephen F
dc.contributor.authorEaston, Christopher
dc.date.accessioned2015-12-13T22:35:19Z
dc.date.issued2005
dc.date.updated2015-12-11T09:27:13Z
dc.description.abstract6A-Deoxy-6A-propynamido-β-cyclodextrin reacts with 4-tert-butylphenyl azide in aqueous solution, to form the 5-(aminocarbonyl)-substituted triazole in preference to the 4-(aminocarbonyl)- substituted analogue, in a ratio of 25:1. The cyclodextrin moiety
dc.identifier.issn1061-0278
dc.identifier.urihttp://hdl.handle.net/1885/76535
dc.publisherTaylor & Francis Group
dc.sourceSupramolecular Chemistry
dc.subjectKeywords: Cycloadditions; Cyclodextrins; Molecular reactors; Regio selectivity; Templates; Triazoles
dc.titleA cyclodextrin molecular reactor for the regioselective synthesis of 1,5-disubstituted-1,2,3-triazoles
dc.typeJournal article
local.bibliographicCitation.issue7
local.bibliographicCitation.lastpage555
local.bibliographicCitation.startpage547
local.contributor.affiliationBarr, Lorna, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationLincoln, Stephen F, University of Adelaide
local.contributor.affiliationEaston, Christopher, College of Physical and Mathematical Sciences, ANU
local.contributor.authoruidBarr, Lorna, u4013429
local.contributor.authoruidEaston, Christopher, u9500570
local.description.embargo2037-12-31
local.description.notesImported from ARIES
local.description.refereedYes
local.identifier.absfor030302 - Nanochemistry and Supramolecular Chemistry
local.identifier.ariespublicationMigratedxPub5349
local.identifier.citationvolume17
local.identifier.doi10.1080/10610270500329131
local.identifier.scopusID2-s2.0-30344441790
local.type.statusPublished Version

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