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Towards a synthesis of naphthalene derived natural products

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dc.contributor.authorMcCulloch, Malcolm
dc.contributor.authorBarrow, Russell
dc.date.accessioned2009-05-21T04:23:37Zen_US
dc.date.accessioned2010-12-20T06:05:02Z
dc.date.available2009-05-21T04:23:37Zen_US
dc.date.available2010-12-20T06:05:02Z
dc.date.issued2005-10-31en_US
dc.date.updated2015-12-12T07:46:04Z
dc.description.abstractDieckmann-type cyclization reactions have been employed in the synthesis of the alkyl substituted naphthoquinone 11 and the naphthalenes 10 and 12. Various conditions for the benzylic oxidation of these compounds have been investigated with a view towards the synthesis of some naphthalene based natural products.
dc.format7 pages
dc.identifier.citationMolecules 10.10 (2005): 1272-1278
dc.identifier.issn1420-3049en_US
dc.identifier.urihttp://hdl.handle.net/10440/296en_US
dc.identifier.urihttp://digitalcollections.anu.edu.au/handle/10440/296
dc.publisherMolecular Diversity Preservation International
dc.rightshttp://www.sherpa.ac.uk/romeo/search.php "Author can archive pre-print (ie pre-refereeing) … [and] post-print (ie final draft post-refereeing) …[and] publisher's version/PDF Published source must be acknowledged; Creative Commons Attribution License; Authors are encouraged to submit their published articles to institutional repositories" from SHERPA/RoMEO site (as as 01/04/10)
dc.sourceMolecules: a journal of synthetic organic and natural products
dc.source.urihttp://www.mdpi.com/1420-3049/10/10/1272/pdfen_US
dc.subjectNaphthalenes
dc.subjectbenzylic oxidation
dc.subjectnaphtho-γ-pyrone
dc.titleTowards a synthesis of naphthalene derived natural products
dc.typeJournal article
dcterms.dateAccepted2005-04-28en_US
local.bibliographicCitation.lastpage1278
local.bibliographicCitation.startpage1272
local.contributor.affiliationMcCulloch, Malcolm, Research School of Earth Sciencesen_US
local.contributor.affiliationBarrow, Russell, Faculty of Science, Department of Chemistryen_US
local.contributor.authoruidU7902024en_US
local.contributor.authoruidU9902002en_US
local.description.notesThis article belongs to the special issue 2004 RACI One-day Natural Products Group Symposium.en_US
local.description.refereedYes
local.identifier.absfor030503en_US
local.identifier.ariespublicationMigratedxPub13058en_US
local.identifier.citationvolume10
local.identifier.doi10.3390/10101272
local.identifier.scopusID2-s2.0-33644799520
local.type.statusPublished Versionen_US

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