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dc.contributor.authorYoung, David
dc.contributor.authorMcCluskey, A.
dc.contributor.authorGarner, J.
dc.contributor.authorCaballero, S.
dc.date.accessioned2017-05-03T13:46:29Z
dc.date.available2017-05-03T13:46:29Z
dc.date.issued2000
dc.identifier.issn00404039
dc.identifier.doi10.1016/S0040-4039(00)01408-8
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%).
dc.description.peerreviewedYes
dc.description.publicationstatusYes
dc.languageEnglish
dc.language.isoeng
dc.publisherPergamon
dc.publisher.placeUK
dc.relation.ispartofpagefrom8147
dc.relation.ispartofpageto8151
dc.relation.ispartofjournalTetrahedron Letters
dc.relation.ispartofvolume41
dc.subject.fieldofresearchHistory and Archaeology
dc.subject.fieldofresearchMedicinal and Biomolecular Chemistry
dc.subject.fieldofresearchOrganic Chemistry
dc.subject.fieldofresearchcode21
dc.subject.fieldofresearchcode0304
dc.subject.fieldofresearchcode0305
dc.titleTetraallylstannane and Weinreb amides: a simple ‘green’ route to N-protected homoallylic alcohols and allyl ketones
dc.typeJournal article
dc.type.descriptionC1 - Articles
dc.type.codeC - Journal Articles
gro.facultyGriffith Sciences, School of Natural Sciences
gro.date.issued2015-05-11T00:46:21Z
gro.hasfulltextNo Full Text
gro.griffith.authorYoung, David


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