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Article: Constitutional isomerism in bicyclic diacetals and the conformational behaviour of cis-fused 1,3,6,8-tetraoxabicyclo[5,3,0]decanes

TitleConstitutional isomerism in bicyclic diacetals and the conformational behaviour of cis-fused 1,3,6,8-tetraoxabicyclo[5,3,0]decanes
Authors
Issue Date1974
Citation
Journal of the Chemical Society, Chemical Communications, 1974, n. 21 How to Cite?
AbstractThe equilibrium proportions of the constitutional isomers (1)-(4) and the conformational behaviour of the cis-fused 1,3,6,8-tetraoxabicyclo[5,3,0]decanes (1a)-(4a) provide no evidence for the gauche arrangement of the vicinal oxygen substituents being a stabilising feature in these systems.
Persistent Identifierhttp://hdl.handle.net/10722/332824
ISSN

 

DC FieldValueLanguage
dc.contributor.authorBurden, Ian J.-
dc.contributor.authorStoddart, J. Fraser-
dc.date.accessioned2023-10-06T05:14:34Z-
dc.date.available2023-10-06T05:14:34Z-
dc.date.issued1974-
dc.identifier.citationJournal of the Chemical Society, Chemical Communications, 1974, n. 21-
dc.identifier.issn0022-4936-
dc.identifier.urihttp://hdl.handle.net/10722/332824-
dc.description.abstractThe equilibrium proportions of the constitutional isomers (1)-(4) and the conformational behaviour of the cis-fused 1,3,6,8-tetraoxabicyclo[5,3,0]decanes (1a)-(4a) provide no evidence for the gauche arrangement of the vicinal oxygen substituents being a stabilising feature in these systems.-
dc.languageeng-
dc.relation.ispartofJournal of the Chemical Society, Chemical Communications-
dc.titleConstitutional isomerism in bicyclic diacetals and the conformational behaviour of cis-fused 1,3,6,8-tetraoxabicyclo[5,3,0]decanes-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1039/C3974000863b-
dc.identifier.scopuseid_2-s2.0-37049142724-
dc.identifier.issue21-

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