Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/86028
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dc.contributor.authorWarrener, R.N.en
dc.contributor.authorPitt, I.G.en
dc.contributor.authorRussell, R.A.en
dc.date.issued1982en
dc.identifier.citationJournal of the Chemical Society, Chemical Communications, 1982; (20):1195-1197en
dc.identifier.issn0022-4936en
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.en
dc.description.statementofresponsibilityRonald N. Warrener, Ian G. Pitt and Richard A. Russellen
dc.language.isoenen
dc.publisherRoyal Society of Chemistryen
dc.rightsCopyright status unknownen
dc.titlePhotodimers of isobenzofuran: a novel application of lanthanide induced shift spectroscopy to determine stereochemistryen
dc.typeJournal articleen
dc.identifier.rmid0030009197en
dc.identifier.doi10.1039/c39820001195en
dc.identifier.pubid102234-
pubs.library.collectionChemistry publicationsen
pubs.library.teamDS02en
pubs.verification-statusVerifieden
pubs.publication-statusPublisheden
Appears in Collections:Chemistry publications

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