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Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/86028
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dc.contributor.authorWarrener, R.N.-
dc.contributor.authorPitt, I.G.-
dc.contributor.authorRussell, R.A.-
dc.date.issued1982-
dc.identifier.citationJournal of the Chemical Society, Chemical Communications, 1982; (20):1195-1197-
dc.identifier.issn0022-4936-
dc.identifier.urihttp://hdl.handle.net/2440/86028-
dc.description.abstractIn aceptone solution u.v. irradiation of isobenzofuran at –60 °C forms an [8 + 8] dimer shown by lanthanide induced shift spectroscopy to have the anti-stereochemistry; in ether solution an [8 + 8] dimer is obtained together with a skeletally modified dimmer, the structure of which is confirmed by synthesis.-
dc.description.statementofresponsibilityRonald N. Warrener, Ian G. Pitt and Richard A. Russell-
dc.language.isoen-
dc.publisherRoyal Society of Chemistry-
dc.rightsCopyright status unknown-
dc.source.urihttp://dx.doi.org/10.1039/c39820001195-
dc.titlePhotodimers of isobenzofuran: a novel application of lanthanide induced shift spectroscopy to determine stereochemistry-
dc.typeJournal article-
dc.identifier.doi10.1039/c39820001195-
pubs.publication-statusPublished-
Appears in Collections:Aurora harvest 7
Chemistry publications

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