Deacylation of 4-nitrophenyl acetate by 6A-(w-aminoalkyl)amino-6A-deoxy-b-cyclodextrins

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dc.contributor.authorRedman, Kahlee
dc.contributor.authorMay, Bruce L
dc.contributor.authorKean, Suzanne Dawn
dc.contributor.authorClements, Philip
dc.contributor.authorEaston, Christopher
dc.contributor.authorLincoln, Stephen F
dc.date.accessioned2015-12-13T23:35:13Z
dc.date.available2015-12-13T23:35:13Z
dc.date.issued1999
dc.date.updated2015-12-12T09:39:08Z
dc.description.abstractThe deacylation of 4-nitrophenyl acetate (pNPA) in aqueous solution to give 4-nitrophenolate is significantly accelerated by the 6A-(ω-aminoalkyl)amino-6A-deoxy-β-cyclodextrins [βCDNH(CH2)nNH2] which are themselves acylated to give predominantly βCDNH
dc.identifier.issn1472-779X
dc.identifier.urihttp://hdl.handle.net/1885/93817
dc.publisherRoyal Society of Chemistry
dc.sourceJournal of the Chemical Society, Perkin Transactions 2
dc.titleDeacylation of 4-nitrophenyl acetate by 6A-(w-aminoalkyl)amino-6A-deoxy-b-cyclodextrins
dc.typeJournal article
local.bibliographicCitation.lastpage1717
local.bibliographicCitation.startpage1711
local.contributor.affiliationRedman, Kahlee, University of Adelaide
local.contributor.affiliationMay, Bruce L, University of Adelaide
local.contributor.affiliationKean, Suzanne Dawn, University of Adelaide
local.contributor.affiliationClements, Philip, University of Adelaide
local.contributor.affiliationEaston, Christopher, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationLincoln, Stephen F, University of Adelaide
local.contributor.authoruidEaston, Christopher, u9500570
local.description.notesImported from ARIES
local.description.refereedYes
local.identifier.absfor030503 - Organic Chemical Synthesis
local.identifier.ariespublicationMigratedxPub25232
local.identifier.scopusID2-s2.0-0000374205
local.type.statusPublished Version

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