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Article: Conformational behaviour of di-o-thymotide and di-o-carvocrotide

TitleConformational behaviour of di-o-thymotide and di-o-carvocrotide
Authors
Ollis, W. DavidStoddart, J. Fraser
Issue Date1973
Citation
Journal of the Chemical Society, Chemical Communications, 1973, n. 16, p. 571-572 How to Cite?
DOI: http://dx.doi.org/10.1039/C39730000571
AbstractThe temperature-dependent 1H n.m.r. spectra of suitably substituted disalicylides [(3) and (4)], related lactones [(8) and (9)], and bislactams [(10) and (11)], demonstrate their ring inversion (B ⇌ B*) between enantiomeric boat conformations.
Persistent Identifierhttp://hdl.handle.net/10722/332817
ISSN
0022-4936
ISI Accession Number ID
WOS:A1973Q489200011

 

DC FieldValueLanguage
dc.contributor.authorOllis, W. David-
dc.contributor.authorStoddart, J. Fraser-
dc.date.accessioned2023-10-06T05:14:31Z-
dc.date.available2023-10-06T05:14:31Z-
dc.date.issued1973-
dc.identifier.citationJournal of the Chemical Society, Chemical Communications, 1973, n. 16, p. 571-572-
dc.identifier.issn0022-4936-
dc.identifier.urihttp://hdl.handle.net/10722/332817-
dc.description.abstractThe temperature-dependent <sup>1</sup>H n.m.r. spectra of suitably substituted disalicylides [(3) and (4)], related lactones [(8) and (9)], and bislactams [(10) and (11)], demonstrate their ring inversion (B ⇌ B*) between enantiomeric boat conformations.-
dc.languageeng-
dc.relation.ispartofJournal of the Chemical Society, Chemical Communications-
dc.titleConformational behaviour of di-o-thymotide and di-o-carvocrotide-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1039/C39730000571-
dc.identifier.scopuseid_2-s2.0-37049129522-
dc.identifier.issue16-
dc.identifier.spage571-
dc.identifier.epage572-
dc.identifier.isiWOS:A1973Q489200011-

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