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Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/4787
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dc.contributor.authorEaston, C.-
dc.contributor.authorHarper, J.-
dc.contributor.authorLincoln, S.-
dc.date.issued1998-
dc.identifier.citationNew Journal of Chemistry: a journal for new directions in chemistry, 1998; 22(11):1163-1165-
dc.identifier.issn1144-0546-
dc.identifier.issn1369-9261-
dc.identifier.urihttp://hdl.handle.net/2440/4787-
dc.description.abstractThe title cyclodextrin dimer biases competing reactions of indoxyl anion to give indirubin and indigo against the latter, due to the preferred geometry of alignment of the cyclodextrin annuli.-
dc.language.isoen-
dc.publisherGAUTHIER-VILLARS/EDITIONS ELSEVIER-
dc.source.urihttp://dx.doi.org/10.1039/a806486e-
dc.titleN,N'-Bis(6A-deoxy-b-cyclodextrin-6A-yl)urea as a molecular template in the formation of indigoid dyes-
dc.typeJournal article-
dc.identifier.doi10.1039/a806486e-
pubs.publication-statusPublished-
Appears in Collections:Aurora harvest 2
Chemistry publications
Environment Institute publications

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