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Article: Configurational equilibria in 2,4-disubstituted-γ-butyrolactones

TitleConfigurational equilibria in 2,4-disubstituted-γ-butyrolactones
Authors
Hussain, S. A.M.TayyebOllis, W. DavidSmith, ChristopherStoddart, J. Fraser
Issue Date1974
Citation
Journal of the Chemical Society, Chemical Communications, 1974, n. 21 How to Cite?
DOI: http://dx.doi.org/10.1039/C3974000873b
AbstractEquilibration studies on seven 2,4-disubstituted-γ-butyrolactones indicate that the cis-isomer is thermodynamically more stable than the trans-isomer in all cases.
Persistent Identifierhttp://hdl.handle.net/10722/332823
ISSN
0022-4936

 

DC FieldValueLanguage
dc.contributor.authorHussain, S. A.M.Tayyeb-
dc.contributor.authorOllis, W. David-
dc.contributor.authorSmith, Christopher-
dc.contributor.authorStoddart, J. Fraser-
dc.date.accessioned2023-10-06T05:14:33Z-
dc.date.available2023-10-06T05:14:33Z-
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/10722/332823-
dc.description.abstractEquilibration studies on seven 2,4-disubstituted-γ-butyrolactones indicate that the cis-isomer is thermodynamically more stable than the trans-isomer in all cases.-
dc.languageeng-
dc.relation.ispartofJournal of the Chemical Society, Chemical Communications-
dc.titleConfigurational equilibria in 2,4-disubstituted-γ-butyrolactones-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1039/C3974000873b-
dc.identifier.scopuseid_2-s2.0-37049139926-
dc.identifier.issue21-

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