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Article: The conformational behaviour of 5,6,11,12,17,18-hexahydrotribenzo[a,e,i]- cyclododecaene and its derivatives

TitleThe conformational behaviour of 5,6,11,12,17,18-hexahydrotribenzo[a,e,i]- cyclododecaene and its derivatives
Authors
Brickwood, David J.Ollis, W. DavidStoddart, J. Fraser
Issue Date1973
Citation
Journal of the Chemical Society, Chemical Communications, 1973, n. 17, p. 638-640 How to Cite?
DOI: http://dx.doi.org/10.1039/C39730000638
AbstractThe temperature dependence of the 1H n.m.r. spectrum of 1,4,7,10,13,16-hexamethyl-5,6,11,12,17,18-hexahydrotribenzo[a,e,i] cyclododecaene (2) has been interpreted in terms of ring inversion between enantiomeric C2 conformations.
Persistent Identifierhttp://hdl.handle.net/10722/332818
ISSN
0022-4936
ISI Accession Number ID
WOS:A1973Q575500039

 

DC FieldValueLanguage
dc.contributor.authorBrickwood, David J.-
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. 17, p. 638-640-
dc.identifier.issn0022-4936-
dc.identifier.urihttp://hdl.handle.net/10722/332818-
dc.description.abstractThe temperature dependence of the <sup>1</sup>H n.m.r. spectrum of 1,4,7,10,13,16-hexamethyl-5,6,11,12,17,18-hexahydrotribenzo[a,e,i] cyclododecaene (2) has been interpreted in terms of ring inversion between enantiomeric C<inf>2</inf> conformations.-
dc.languageeng-
dc.relation.ispartofJournal of the Chemical Society, Chemical Communications-
dc.titleThe conformational behaviour of 5,6,11,12,17,18-hexahydrotribenzo[a,e,i]- cyclododecaene and its derivatives-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1039/C39730000638-
dc.identifier.scopuseid_2-s2.0-37049130998-
dc.identifier.issue17-
dc.identifier.spage638-
dc.identifier.epage640-
dc.identifier.isiWOS:A1973Q575500039-

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