Allylation of β-ketoaldehydes and functionalized imines by diallyltin dibromide: Formation of skipped and conjugated dienes

dc.contributor.author Kumaraswamy, Sudha
dc.contributor.author Nagabrahmanandachari, S.
dc.contributor.author Swamy, K. C.Kumara
dc.date.accessioned 2022-03-27T09:58:06Z
dc.date.available 2022-03-27T09:58:06Z
dc.date.issued 1996-01-01
dc.description.abstract Diallyltin dibromide reacts with β-ketoaldehydes possessing no aromatic side groups and with (hydroxy) aryl imines to afford the expected homoallyl alcohols or amines respectively. With β-ketoaldehydes having aromatic side groups, skipped or conjugated dienes are obtained depending on whether or not an aqueous work up procedure is used.
dc.identifier.citation Synthetic Communications. v.26(4)
dc.identifier.issn 00397911
dc.identifier.uri 10.1080/00397919608086748
dc.identifier.uri http://www.tandfonline.com/doi/abs/10.1080/00397919608086748
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/13483
dc.title Allylation of β-ketoaldehydes and functionalized imines by diallyltin dibromide: Formation of skipped and conjugated dienes
dc.type Journal. Article
dspace.entity.type
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