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The synthetic versatility of alkoxycarbonyl- and hydroxymethyl-piperazine-2,5-diones

Chai, Christina; Driver, J; Huleatt, Paul

Description

Alkoxycarbonylpiperazine-2,5-diones are versatile precursors for the α-functionalisation of piperazine-2,5-diones. The alkoxycarbonyl group activates the α-carbon position to alkylation reactions and this provides a mild and selective method for the ext

dc.contributor.authorChai, Christina
dc.contributor.authorDriver, J
dc.contributor.authorHuleatt, Paul
dc.date.accessioned2015-12-13T23:02:22Z
dc.identifier.issn0040-4020
dc.identifier.urihttp://hdl.handle.net/1885/84857
dc.description.abstractAlkoxycarbonylpiperazine-2,5-diones are versatile precursors for the α-functionalisation of piperazine-2,5-diones. The alkoxycarbonyl group activates the α-carbon position to alkylation reactions and this provides a mild and selective method for the ext
dc.publisherElsevier
dc.sourceTetrahedron
dc.subjectKeywords: carbon; carboxyl group; functional group; imine; ion; piperazine derivative; piperazinedione; alkylation; article; atom; chemistry; precursor; priority journal; reaction analysis; stereochemistry; synthesis Alkylations; Amino acids and derivatives; N-Acyliminium ions; Trapping reactions
dc.titleThe synthetic versatility of alkoxycarbonyl- and hydroxymethyl-piperazine-2,5-diones
dc.typeJournal article
local.description.notesImported from ARIES
local.description.refereedYes
local.identifier.citationvolume61
dc.date.issued2005
local.identifier.absfor060310 - Plant Systematics and Taxonomy
local.identifier.ariespublicationMigratedxPub13089
local.type.statusPublished Version
local.contributor.affiliationChai, Christina, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationDriver, J, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationHuleatt, Paul, College of Physical and Mathematical Sciences, ANU
local.description.embargo2037-12-31
local.bibliographicCitation.issue36
local.bibliographicCitation.startpage8722
local.bibliographicCitation.lastpage8739
local.identifier.doi10.1016/j.tet.2005.06.084
dc.date.updated2015-12-12T07:46:33Z
local.identifier.scopusID2-s2.0-23444431603
CollectionsANU Research Publications

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