Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/85864
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dc.contributor.authorTan, R.Y.S.-
dc.contributor.authorRussell, R.A.-
dc.contributor.authorWarrener, R.N.-
dc.date.issued1981-
dc.identifier.citationAustralian Journal of Chemistry: an international journal for chemical science, 1981; 34(4):905-911-
dc.identifier.issn0004-9425-
dc.identifier.issn1445-0038-
dc.identifier.urihttp://hdl.handle.net/2440/85864-
dc.description.abstractReaction of the 7,8-dichlorobicyclo[4,2,0]octa-2,4-diene (9) with 2,3-dichloro-5,6-dicyano-1,4-benzoquinone yields the benzocyclobutene (10). Extension of this technique to the related bicyclo[4,2,0]octa-2,4,7-trienes (21) and (23), or 8-oxatricyclo[4,3,0,07,9]nona-2,4-diene (6) was unsuccessful. Manganese dioxide was equally unrewarding while o-chloranil reacted with these olefins to yield benzodioxins in a [4+2] cycloaddition reaction.-
dc.description.statementofresponsibilityRichard Y. S. Tan, Richard A. Russell and, Ronald N. Warrener-
dc.language.isoen-
dc.publisherCSIRO Publishing-
dc.rights© CSIRO 1981-
dc.titleAn investigation of the reaction of dehydrogenating agents with a stable 8-Oxatricyclo[4,3,0,0⁷,⁹]nona-2,4-diene and related Bicylo[4,2,0]octa-2,4-dienes as a potential route to isobenzofurans-
dc.title.alternativeAn investigation of the reaction of dehydrogenating agents with a stable 8-Oxatricyclo[4,3,0,0(7),(9)]nona-2,4-diene and related Bicylo[4,2,0]octa-2,4-dienes as a potential route to isobenzofurans-
dc.typeJournal article-
dc.identifier.doi10.1071/CH9810905-
pubs.publication-statusPublished-
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