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Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/57161
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dc.contributor.authorAbell, A.-
dc.contributor.authorAlexander, N.-
dc.contributor.authorAitken, S.-
dc.contributor.authorChen, H.-
dc.contributor.authorCoxon, J.-
dc.contributor.authorJones, M.-
dc.contributor.authorMcNabb, S.-
dc.contributor.authorMuscroft-Taylor, A.-
dc.date.issued2009-
dc.identifier.citationJournal of Organic Chemistry, 2009; 74(11):4354-4356-
dc.identifier.issn0022-3263-
dc.identifier.issn1520-6904-
dc.identifier.urihttp://hdl.handle.net/2440/57161-
dc.description.abstractWe report the synthesis of macrocycles 1-6 via ring closing metathesis of dienes 7-12. Addition of chlorodicyclohexylborane to thermal and microwave assisted RCM of dienes 8 and 9 markedly improves the yield. The geometric isomers of macrocycles 1-3 and 5 have been assigned using X-ray crystallography and NMR.-
dc.description.statementofresponsibilityAndrew D. Abell, Nathan A. Alexander, Steven G. Aitken, Hongyuan Chen, James M. Coxon, Matthew A. Jones, Stephen B. McNabb and Andrew Muscroft-Taylor-
dc.language.isoen-
dc.publisherAmer Chemical Soc-
dc.rights© 2009 American Chemical Society-
dc.source.urihttp://dx.doi.org/10.1021/jo802723w-
dc.titleSynthesis of macrocyclic β-Strand memplates by ring closing metathesis-
dc.title.alternativeSynthesis of macrocyclic beta-Strand memplates by ring closing metathesis-
dc.typeJournal article-
dc.identifier.doi10.1021/jo802723w-
dc.relation.grantARC-
pubs.publication-statusPublished-
dc.identifier.orcidAbell, A. [0000-0002-0604-2629]-
Appears in Collections:Aurora harvest
Chemistry publications

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