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A metalation stratagy for the construction of functionalized naphthalenes: the first synthesis of guieranone A

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dc.contributor.authorMcCulloch, Malcolm
dc.contributor.authorBarrow, Russell
dc.date.accessioned2015-12-13T22:57:48Z
dc.date.issued2005
dc.date.updated2015-12-12T07:18:49Z
dc.description.abstractThe first synthesis of the natural product guieranone A is described, demonstrating a one-pot procedure for the synthesis of protected-1,3,6,8- tetraoxygenated naphthalenes and a subsequent directed metalation synthesis of 2-keto naphthalenes.
dc.identifier.issn0040-4039
dc.identifier.urihttp://hdl.handle.net/1885/83146
dc.publisherElsevier
dc.sourceTetrahedron Letters
dc.subjectKeywords: antifungal agent; guieranone a; naphthalene derivative; natural product; unclassified drug; article; chemical reaction; drug synthesis; oxygenation Dieckmann cyclization; Guieranone; Metalation; Naphthalenes; Natural product
dc.titleA metalation stratagy for the construction of functionalized naphthalenes: the first synthesis of guieranone A
dc.typeJournal article
local.bibliographicCitation.lastpage7621
local.bibliographicCitation.startpage7619
local.contributor.affiliationMcCulloch, Malcolm, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationBarrow, Russell, College of Physical and Mathematical Sciences, ANU
local.contributor.authoruidMcCulloch, Malcolm, u7902024
local.contributor.authoruidBarrow, Russell, u9902002
local.description.embargo2037-12-31
local.description.notesImported from ARIES
local.description.refereedYes
local.identifier.absfor030599 - Organic Chemistry not elsewhere classified
local.identifier.ariespublicationMigratedxPub11355
local.identifier.citationvolume46
local.identifier.doi10.1016/j.tetlet.2005.08.127
local.identifier.scopusID2-s2.0-26244468386
local.type.statusPublished Version

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