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Article: Stereospecific synthesis of the trans-anti-trans- and trans-syn-trans- isomers of dicyclohexyl-18-crown-6

TitleStereospecific synthesis of the trans-anti-trans- and trans-syn-trans- isomers of dicyclohexyl-18-crown-6
Authors
Issue Date1974
Citation
Journal of the Chemical Society, Chemical Communications, 1974, n. 10, p. 390-391 How to Cite?
AbstractThe macrocyclic polyethers, (7) and (8), have been synthesised stereospecifically from the diastereoisomeric acyclic methylene acetals, (1) and (2), obtained from (±)-cyclohexane-trans-1,2-diol; both (7) and (8) form stable complexes with metal cations.
Persistent Identifierhttp://hdl.handle.net/10722/332813
ISSN
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorStoddart, J. Fraser-
dc.contributor.authorWheatley, Colin M.-
dc.date.accessioned2023-10-06T05:14:28Z-
dc.date.available2023-10-06T05:14:28Z-
dc.date.issued1974-
dc.identifier.citationJournal of the Chemical Society, Chemical Communications, 1974, n. 10, p. 390-391-
dc.identifier.issn0022-4936-
dc.identifier.urihttp://hdl.handle.net/10722/332813-
dc.description.abstractThe macrocyclic polyethers, (7) and (8), have been synthesised stereospecifically from the diastereoisomeric acyclic methylene acetals, (1) and (2), obtained from (±)-cyclohexane-trans-1,2-diol; both (7) and (8) form stable complexes with metal cations.-
dc.languageeng-
dc.relation.ispartofJournal of the Chemical Society, Chemical Communications-
dc.titleStereospecific synthesis of the trans-anti-trans- and trans-syn-trans- isomers of dicyclohexyl-18-crown-6-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1039/C39740000390-
dc.identifier.scopuseid_2-s2.0-37049114434-
dc.identifier.issue10-
dc.identifier.spage390-
dc.identifier.epage391-
dc.identifier.isiWOS:A1974T056800029-

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