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Asymmetric synthesis of N-aryl aziridines

dc.contributor.authorAires-de-Sousa, João
dc.contributor.authorPrabhakar, Sundaresan
dc.contributor.authorLobo, Ana M.
dc.contributor.authorRosa, Ana M.
dc.contributor.authorGomes, Mário
dc.contributor.authorCorvo, Marta C.
dc.contributor.authorWilliams, David J.
dc.contributor.authorWhite, Andrew J.
dc.date.accessioned2012-01-06T14:47:44Z
dc.date.available2012-01-06T14:47:44Z
dc.date.issued2001
dc.description.abstractThe reactions of a variety of N-arylhydroxamates as nitrogen transfer reagents to acryloyl derivatives of (−)-8-phenylmenthol, (−)-quinine and (−)-Oppolzer’s sultam acting as Michael acceptors was studied. Poor to modest diastereoselection was observed in the formation of aziridines. The absolute structure of one of the pure diastereomers secured from Oppolzer’s auxiliary was established by X-ray crystallography and hence the absolute configuration of the derived methyl-N-phenylaziridine-2-carboxylate could be assigned. Whilst only poor facial selectivity was observed for chiral hydroxamic acid prepared from dehydroabietic acid, moderate to good enantioselection of aziridines could be achieved with the chiral quaternary salts based on cinchona alkaloids, especially with that of cinchonine. A model is presented to explain the origin of enantioselection and a mechanism is proposed for the aziridination reaction.por
dc.identifier.citationAires-de-Sousa J, Prabhakar S, Lobo AM, Rosa AM, Gomes M, Corvo MC, Williams DJ, White AJ. Asymmetric synthesis of N-aryl aziridines. Tetrahedron Asymmetry. 2001;12:3349-65.por
dc.identifier.issn1362-511X
dc.identifier.urihttp://hdl.handle.net/10400.21/1017
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherPergamonpor
dc.relation.publisherversionhttp://www.ingentaconnect.com/content/els/09574166/2002/00000012/00000024/art00548por
dc.subjectChemistrypor
dc.subjectAziridinespor
dc.titleAsymmetric synthesis of N-aryl aziridinespor
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage3365por
oaire.citation.startPage3349por
oaire.citation.titleTetrahedron Asymmetrypor
rcaap.rightsrestrictedAccesspor
rcaap.typearticlepor

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