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Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/4790
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dc.contributor.authorOnagi, H.-
dc.contributor.authorEaston, C.-
dc.contributor.authorLincoln, S.-
dc.date.issued2001-
dc.identifier.citationOrganic Letters, 2001; 3(7):1041-1044-
dc.identifier.issn1523-7060-
dc.identifier.issn1523-7052-
dc.identifier.urihttp://hdl.handle.net/2440/4790-
dc.descriptionCopyright © 2001 American Chemical Society-
dc.description.abstract(matrix presented) The pictured rotaxane is assembled in water by capping a substituted cyclodextrin composed of the wheel and axle components. The unusual dimeric structure of the rotaxane reflects the thermodynamics of the assembly process. In N,N-dimethylformamide, the corresponding monomer is the predominant product.-
dc.description.statementofresponsibilityHideki Onagi, Christopher J. Easton, and Stephen F. Lincoln-
dc.language.isoen-
dc.publisherAmer Chemical Soc-
dc.source.urihttp://dx.doi.org/10.1021/ol015607e-
dc.titleAn hermaphrodite [2]rotaxane: Preparation and analysis of structure-
dc.typeJournal article-
dc.identifier.doi10.1021/ol015607e-
pubs.publication-statusPublished-
Appears in Collections:Aurora harvest 6
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