Iodine induced transfer of dialkylvinylboranes produced by the hydridation of dialkylhaloboranes in the presence of 1-alkynes. Generalization of the zweifel cis- alkene synthesis

dc.contributor.author Kulkarni, Urendra U.
dc.contributor.author Basavaiah, D.
dc.contributor.author Brown, Herbert C.
dc.date.accessioned 2022-03-27T09:05:58Z
dc.date.available 2022-03-27T09:05:58Z
dc.date.issued 1982-02-01
dc.description.abstract Dialkylvinylboranes, prepared conveniently via the hydridation of dialkylhaloboranes in the presence of terminal alkynes, react with iodine in the presence of a base at reduced temperatures to form the corresponding cis-disubstituted alkenes. This development greatly increases the generality of the elegant weifel cis-olefin synthesis. © 1982.
dc.identifier.citation Journal of Organometallic Chemistry. v.225(1)
dc.identifier.issn 0022328X
dc.identifier.uri 10.1016/S0022-328X(00)86837-0
dc.identifier.uri https://www.sciencedirect.com/science/article/abs/pii/S0022328X00868370
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/12412
dc.title Iodine induced transfer of dialkylvinylboranes produced by the hydridation of dialkylhaloboranes in the presence of 1-alkynes. Generalization of the zweifel cis- alkene synthesis
dc.type Journal. Article
dspace.entity.type
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