Square pegs in round holes. Preparation and intramolecular complexation of cubyl substituted b-cyclodextrins and of an adamantane analog

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dc.contributor.authorMay, Bruce L
dc.contributor.authorClements, Philip
dc.contributor.authorTsanaktsidis, J
dc.contributor.authorEaston, Christopher
dc.contributor.authorLincoln, Stephen F
dc.date.accessioned2015-12-13T23:16:43Z
dc.date.available2015-12-13T23:16:43Z
dc.date.issued2000
dc.date.updated2015-12-12T08:49:20Z
dc.description.abstractThe reaction of either 1-methoxycarbonyl-4-(4-nitrophenoxycarbonyl)cubane or its dimethyl analogue, 2,3-dimethyl-1-methoxycarbonyl-4-(4-nitrophenoxycarbonyl)cubane, with the primary amine of 6A-(6-amino-hexyl)amino-6A-deoxy-β-cyclodextrin produces the fi
dc.identifier.issn1470-4358
dc.identifier.urihttp://hdl.handle.net/1885/89549
dc.publisherRoyal Society of Chemistry
dc.sourceJournal of the Chemical Society, Perkin Transactions 1
dc.subjectKeywords: Hydrophobicity; Molecular structure; Nuclear magnetic resonance; Organic compounds; Intermolecular complexation; Complexation
dc.titleSquare pegs in round holes. Preparation and intramolecular complexation of cubyl substituted b-cyclodextrins and of an adamantane analog
dc.typeJournal article
local.bibliographicCitation.lastpage469
local.bibliographicCitation.startpage463
local.contributor.affiliationMay, Bruce L, University of Adelaide
local.contributor.affiliationClements, Philip, University of Adelaide
local.contributor.affiliationTsanaktsidis, J, CSIRO Molecular Science
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.ariespublicationMigratedxPub19611
local.identifier.citationvolume3
local.identifier.scopusID2-s2.0-0034615216
local.type.statusPublished Version

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