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Guidelines for stereocontrolled Diels-Alder reactions of chiral methylidene piperazine-2,5-diones with cyclopentadiene

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dc.contributor.authorBurkett, Brenden
dc.contributor.authorChai, Christina
dc.date.accessioned2015-12-13T23:27:20Z
dc.date.issued2001
dc.date.updated2015-12-12T09:49:56Z
dc.description.abstractThe reactivities and stereoselectivities of Diels-Alder cycloaddition reactions of methylidene piperazine-2,5-diones with cyclopentadiene can be manipulated by appropriate choice of N- and α-carbon substituents. Good to excellent exo/endo and facial sele
dc.identifier.issn0040-4039
dc.identifier.urihttp://hdl.handle.net/1885/93278
dc.publisherElsevier
dc.sourceTetrahedron Letters
dc.subjectKeywords: aliphatic compound; amino acid; amino acid derivative; bicyclo compound; carbon; cyclopentadiene derivative; methyl group; methylidene piperazine 2,5 dione derivative; nitrogen derivative; piperazinedione; unclassified drug; article; chemical reaction; ch Amino acids and derivatives; Bicyclic aliphatic compounds; Diels-Alder reactions
dc.titleGuidelines for stereocontrolled Diels-Alder reactions of chiral methylidene piperazine-2,5-diones with cyclopentadiene
dc.typeJournal article
local.bibliographicCitation.issue11
local.bibliographicCitation.lastpage2242
local.bibliographicCitation.startpage2239
local.contributor.affiliationBurkett, Brenden, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationChai, Christina, College of Physical and Mathematical Sciences, ANU
local.contributor.authoruidBurkett, Brenden, u9505013
local.contributor.authoruidChai, Christina, u8615775
local.description.embargo2037-12-31
local.description.notesImported from ARIES
local.description.refereedYes
local.identifier.absfor030503 - Organic Chemical Synthesis
local.identifier.ariespublicationMigratedxPub26681
local.identifier.citationvolume42
local.identifier.doi10.1016/S0040-4039(01)00151-4
local.identifier.scopusID2-s2.0-0035843445
local.type.statusPublished Version

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