Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/86625
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dc.contributor.authorAbell, A.D.-
dc.contributor.authorMassywestropp, R.A.-
dc.date.issued1985-
dc.identifier.citationAustralian Journal of Chemistry: an international journal for chemical science, 1985; 38(7):1031-1036-
dc.identifier.issn0004-9425-
dc.identifier.issn1445-0038-
dc.identifier.urihttp://hdl.handle.net/2440/86625-
dc.description.abstractThe reaction of methylmagnesium iodide with methyl (1R,3S,5R)-1-(furan- 3′-yl)-5-methyl-2,8-dioxabicyclo[3.2.1]octane-3-carboxylate (2) gives products arising from regioselective carbon-oxygen bond fission and intermolecular transfer of the methyl group of the Grignard reagent to the intermediate oxocarbonium ion, in addition to the usual tertiary alcohol.-
dc.description.statementofresponsibilityAD Abell and RA Massy-Westropp-
dc.language.isoen-
dc.publisherCSIRO Publishing-
dc.rights© CSIRO 1985-
dc.titleMechanism of acetal cleavage with methylmagnesium iodide-
dc.typeJournal article-
dc.identifier.doi10.1071/CH9851031-
pubs.publication-statusPublished-
dc.identifier.orcidAbell, A.D. [0000-0002-0604-2629]-
Appears in Collections:Aurora harvest 2
Chemistry publications

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