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Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/48130
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dc.contributor.authorPfeffer, F.-
dc.contributor.authorRussell, R.-
dc.date.issued2002-
dc.identifier.citationOrganic and Biomolecular Chemistry, 2002; 1(23):2680-2685-
dc.identifier.issn1472-7781-
dc.identifier.issn1364-5463-
dc.identifier.urihttp://hdl.handle.net/2440/48130-
dc.descriptionFirst published online 05 Nov 2002-
dc.description.abstractPolynorbornanes with differing edge functionality have been synthesised from the appropriate cyclobutene epoxides substituted with two, unlike, electron withdrawing groups. These latter compounds were prepared by the monohydrolysis of symmetric cyclobutene diesters and subsequent elaboration of the resulting carboxylic acid.-
dc.description.statementofresponsibilityFrederick M. Pfeffer and Richard A. Russell-
dc.language.isoen-
dc.publisherRoyal Society of Chemistry-
dc.rights© The Royal Society of Chemistry 2002-
dc.source.urihttp://www.rsc.org/Publishing/Journals/P1/article.asp?doi=b206057d-
dc.titleSynthesis of [n]polynorbornanes with differing edge substitution: a new class of regioselectively addressable framework-
dc.typeJournal article-
dc.identifier.doi10.1039/b206057d-
pubs.publication-statusPublished-
Appears in Collections:Adelaide Graduate Centre publications
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