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Article: Acid-catalysed rearrangement of caryophyllene oxide

TitleAcid-catalysed rearrangement of caryophyllene oxide
Authors
Issue Date1996
PublisherRoyal Society of Chemistry. The Journal's web site is located at http://www.rsc.org/perkin1
Citation
Journal of Royal Chemical Society Perkin Transactions 1, 1996, v. 1, p. 2507-2509 How to Cite?
AbstractOne of the major products 2 from the reaction of caryophyllene oxide in sulfuric acid is shown to arise from rearrangement of the exocyclic double bond and 1,2-epoxide of the starting material to an endocyclic double bond and 1,4-epoxide system. A hydrated 1,5-epoxide was isolated as a minor component of the reaction.
Persistent Identifierhttp://hdl.handle.net/10722/225237
ISSN
2004 Impact Factor: 2.42

 

DC FieldValueLanguage
dc.contributor.authorTsui, W.Y.,-
dc.contributor.authorBrown, GD-
dc.date.accessioned2016-04-29T01:58:50Z-
dc.date.available2016-04-29T01:58:50Z-
dc.date.issued1996-
dc.identifier.citationJournal of Royal Chemical Society Perkin Transactions 1, 1996, v. 1, p. 2507-2509-
dc.identifier.issn1472-7781-
dc.identifier.urihttp://hdl.handle.net/10722/225237-
dc.description.abstractOne of the major products 2 from the reaction of caryophyllene oxide in sulfuric acid is shown to arise from rearrangement of the exocyclic double bond and 1,2-epoxide of the starting material to an endocyclic double bond and 1,4-epoxide system. A hydrated 1,5-epoxide was isolated as a minor component of the reaction.-
dc.languageeng-
dc.publisherRoyal Society of Chemistry. The Journal's web site is located at http://www.rsc.org/perkin1-
dc.relation.ispartofJournal of Royal Chemical Society Perkin Transactions 1-
dc.titleAcid-catalysed rearrangement of caryophyllene oxide-
dc.typeArticle-
dc.identifier.emailBrown, GD: gdbrown@hkucc.hku.hk-
dc.identifier.doi10.1039/P19960002507-
dc.identifier.hkuros21630-
dc.identifier.volume1-
dc.identifier.spage2507-
dc.identifier.epage2509-
dc.publisher.placeUnited Kingdom-

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