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Article: 1,6,13,18,25,30-hexaoxa[6.6.6](1,3,5)cyclophane. attempted synthesis of a [4] cryptand

Title1,6,13,18,25,30-hexaoxa[6.6.6](1,3,5)cyclophane. attempted synthesis of a [4] cryptand
Authors
Issue Date1977
Citation
Journal of the Chemical Society, Perkin Transactions 1, 1977, p. 785-788 How to Cite?
AbstractThe hexaoxa[5.5.5] (1.3.5)cyclophane (12) has been synthesised from phloroglucinol and 1.4-dibromobutane by using a stepwise approach. All attempts to effect catalytic hydrogenation of both aromatic rings in the hexaoxa- [6.6.6] (1.3.5)cyclophane (12) to give the desired [4]cryptand (14) have proved unsuccessful. © 1977, Royal Society of Chemistry.
Persistent Identifierhttp://hdl.handle.net/10722/332798
ISSN
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorDavid Curtis, W.-
dc.contributor.authorStoddart, J. Fraser-
dc.contributor.authorJones, Graham H.-
dc.date.accessioned2023-10-06T05:14:22Z-
dc.date.available2023-10-06T05:14:22Z-
dc.date.issued1977-
dc.identifier.citationJournal of the Chemical Society, Perkin Transactions 1, 1977, p. 785-788-
dc.identifier.issn1470-4358-
dc.identifier.urihttp://hdl.handle.net/10722/332798-
dc.description.abstractThe hexaoxa[5.5.5] (1.3.5)cyclophane (12) has been synthesised from phloroglucinol and 1.4-dibromobutane by using a stepwise approach. All attempts to effect catalytic hydrogenation of both aromatic rings in the hexaoxa- [6.6.6] (1.3.5)cyclophane (12) to give the desired [4]cryptand (14) have proved unsuccessful. © 1977, Royal Society of Chemistry.-
dc.languageeng-
dc.relation.ispartofJournal of the Chemical Society, Perkin Transactions 1-
dc.title1,6,13,18,25,30-hexaoxa[6.6.6](1,3,5)cyclophane. attempted synthesis of a [4] cryptand-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1039/P19770000785-
dc.identifier.scopuseid_2-s2.0-37049102027-
dc.identifier.spage785-
dc.identifier.epage788-
dc.identifier.isiWOS:A1977DE17900014-

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