Methyl cyanoformate (Mander's reagent)

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dc.contributor.authorBissember, Alexander
dc.date.accessioned2015-12-10T22:28:39Z
dc.date.issued2009
dc.date.updated2015-12-09T09:49:39Z
dc.description.abstract(A) Numerous syntheses of natural products and related compounds have featured the use of methyl cyanoformate to prepare β-keto esters. In the first total syntheses of (+)-lyconadin A and (-)-lyconadin B, Smith and co-workers10 employed Mander's reagent
dc.identifier.issn0936-5214
dc.identifier.urihttp://hdl.handle.net/1885/54551
dc.publisherGeorg Thieme Verlag
dc.sourceSynlett
dc.titleMethyl cyanoformate (Mander's reagent)
dc.typeJournal article
local.bibliographicCitation.issue4
local.bibliographicCitation.lastpage682
local.bibliographicCitation.startpage681
local.contributor.affiliationBissember, Alexander, College of Physical and Mathematical Sciences, ANU
local.contributor.authoruidBissember, Alexander, u3951047
local.description.embargo2037-12-31
local.description.notesImported from ARIES
local.identifier.absfor030503 - Organic Chemical Synthesis
local.identifier.ariespublicationu4005981xPUB304
local.identifier.citationvolume2009
local.identifier.doi10.1055/s-0028-1087716
local.identifier.scopusID2-s2.0-62249176980
local.type.statusPublished Version

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