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dc.contributor.authorYoung, Daviden_US
dc.contributor.authorMcCluskey, A.en_US
dc.contributor.authorGarner, J.en_US
dc.contributor.authorCaballero, S.en_US
dc.date.accessioned2017-04-24T10:58:13Z
dc.date.available2017-04-24T10:58:13Z
dc.date.issued2000en_US
dc.identifier.issn00404039en_US
dc.identifier.doi10.1016/S0040-4039(00)01408-8en_US
dc.identifier.urihttp://hdl.handle.net/10072/3129
dc.description.abstractWe have explored the addition of tetraallylstannane (7) to a variety of N-protected Weinreb amides (N-phthalimido and N-benzyl). Reactions were conducted in methanol and the ionic liquid, butylmethylimidazole tetrafluoroborate (bmim[BF4]), yields of the corresponding N-protected allylketones were moderate to good. Allylation of the corresponding aminoaldehydes gave excellent yields of homoallylic alcohols (68-94%) and moderate to good diastereoselectivities (50-86%).en_US
dc.description.peerreviewedYesen_US
dc.description.publicationstatusYesen_US
dc.languageEnglishen_US
dc.language.isoen_US
dc.publisherPergamonen_US
dc.publisher.placeUKen_US
dc.relation.ispartofpagefrom8147en_US
dc.relation.ispartofpageto8151en_US
dc.relation.ispartofjournalTetrahedron Lettersen_US
dc.relation.ispartofvolume41en_US
dc.subject.fieldofresearchHISTORY AND ARCHAEOLOGYen_US
dc.subject.fieldofresearchcode210000en_US
dc.titleTetraallylstannane and Weinreb amides: a simple ‘green’ route to N-protected homoallylic alcohols and allyl ketonesen_US
dc.typeJournal articleen_US
dc.type.descriptionC1 - Peer Reviewed (HERDC)en_US
dc.type.codeC - Journal Articlesen_US
gro.facultyGriffith Sciences, School of Natural Sciencesen_US
gro.date.issued2015-05-11T00:46:21Z
gro.hasfulltextNo Full Text


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