Unusual reactivity of selenoboranes towards epoxides: New selective routes to beta- hydroxyselenides and allylalcohols

Please use this identifier to cite or link to this item: http://hdl.handle.net/10400.1/6162

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DC Field	Value	Language
dc.contributor.author	Cravador, A.	-
dc.contributor.author	Krief, A.	-
dc.date.accessioned	2015-06-15T09:15:56Z	-
dc.date.available	2015-06-15T09:15:56Z	-
dc.date.issued	1981	-
dc.identifier.issn	0040-4039	-
dc.identifier.other	AUT: ACR00659;	-
dc.identifier.uri	http://hdl.handle.net/10400.1/6162	-
dc.description.abstract	Selenoboranes react with terminal, α, β-di- and trisubstituted epoxides to produce β-hydroxyselenides (or olefins) in the two first cases and allyl alcohols in the last one. A very high stereodescrimination has been observed for α, β-bisubstituted epoxides: the cis epoxide being much more reactive.	pt_PT
dc.language.iso	eng	-
dc.publisher	Pergamon- Elsevier Science, Ltd	-
dc.relation.isbasedon	P-009-32Z	-
dc.rights	restrictedAccess	-
dc.title	Unusual reactivity of selenoboranes towards epoxides: New selective routes to beta- hydroxyselenides and allylalcohols	-
dc.type	article	-
degois.publication.firstPage	2491	-
degois.publication.lastPage	2494	-
degois.publication.title	Tetrahedron Letters	-
dc.peerreviewed	yes	-
degois.publication.volume	22	-
dc.identifier.doi	https://dx.doi.org/10.1016/S0040-4039(01)92941-7	-
Appears in Collections:	FCT2-Artigos (em revistas ou actas indexadas)

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