dc.contributor.author | Young, David | |
dc.contributor.author | McCluskey, A. | |
dc.contributor.author | Garner, J. | |
dc.contributor.author | Caballero, S. | |
dc.date.accessioned | 2017-05-03T13:46:29Z | |
dc.date.available | 2017-05-03T13:46:29Z | |
dc.date.issued | 2000 | |
dc.identifier.issn | 00404039 | |
dc.identifier.doi | 10.1016/S0040-4039(00)01408-8 | |
dc.identifier.uri | http://hdl.handle.net/10072/3129 | |
dc.description.abstract | We 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.peerreviewed | Yes | |
dc.description.publicationstatus | Yes | |
dc.language | English | |
dc.language.iso | eng | |
dc.publisher | Pergamon | |
dc.publisher.place | UK | |
dc.relation.ispartofpagefrom | 8147 | |
dc.relation.ispartofpageto | 8151 | |
dc.relation.ispartofjournal | Tetrahedron Letters | |
dc.relation.ispartofvolume | 41 | |
dc.subject.fieldofresearch | History and Archaeology | |
dc.subject.fieldofresearch | Medicinal and Biomolecular Chemistry | |
dc.subject.fieldofresearch | Organic Chemistry | |
dc.subject.fieldofresearchcode | 21 | |
dc.subject.fieldofresearchcode | 0304 | |
dc.subject.fieldofresearchcode | 0305 | |
dc.title | Tetraallylstannane and Weinreb amides: a simple ‘green’ route to N-protected homoallylic alcohols and allyl ketones | |
dc.type | Journal article | |
dc.type.description | C1 - Articles | |
dc.type.code | C - Journal Articles | |
gro.faculty | Griffith Sciences, School of Natural Sciences | |
gro.date.issued | 2015-05-11T00:46:21Z | |
gro.hasfulltext | No Full Text | |
gro.griffith.author | Young, David | |