Base-promoted reactions of dichlorocarbene adducts of cyclic enamines: A new route to annulated pyrroles

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dc.contributor.authorBissember, Alexander
dc.contributor.authorPhillis, Andrew
dc.contributor.authorBanwell, Martin
dc.contributor.authorWillis, Anthony
dc.date.accessioned2015-12-10T21:56:47Z
dc.date.issued2007
dc.date.updated2015-12-09T07:41:07Z
dc.description.abstractTreatment of the gem-dihalogenocyclopropanes 1-5 with potassium tert-butoxide or LDA results in the formation of the corresponding and annulated pyrroles 13-17, respectively.
dc.identifier.issn1523-7060
dc.identifier.urihttp://hdl.handle.net/1885/39597
dc.publisherAmerican Chemical Society
dc.sourceOrganic Letters
dc.titleBase-promoted reactions of dichlorocarbene adducts of cyclic enamines: A new route to annulated pyrroles
dc.typeJournal article
local.bibliographicCitation.issue26
local.bibliographicCitation.lastpage5424
local.bibliographicCitation.startpage5421
local.contributor.affiliationBissember, Alexander, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationPhillis, Andrew, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationBanwell, Martin, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationWillis, Anthony, College of Physical and Mathematical Sciences, ANU
local.contributor.authoruidBissember, Alexander, u3951047
local.contributor.authoruidPhillis, Andrew, u4069769
local.contributor.authoruidBanwell, Martin, u9500594
local.contributor.authoruidWillis, Anthony, u8512028
local.description.embargo2037-12-31
local.description.notesImported from ARIES
local.identifier.absfor030503 - Organic Chemical Synthesis
local.identifier.ariespublicationu4005981xPUB180
local.identifier.citationvolume9
local.identifier.doi10.1021/ol7021774
local.identifier.scopusID2-s2.0-38349137465
local.type.statusPublished Version

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