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Article: Ambient arylmagnesiation of alkynes catalysed by ligandless nickel(ii)

TitleAmbient arylmagnesiation of alkynes catalysed by ligandless nickel(ii)
Authors
Issue Date2013
Citation
Chemical Communications, 2013, v. 49, n. 86, p. 10121-10123 How to Cite?
AbstractA simple and efficient catalytic arylmagnesiation of diarylacetylenes and aryl(alkyl)acetylenes is accomplished by NiCl2·6H2O at r.t. in the absence of stabilising ligands. The corresponding tetra-substituted alkenes can be obtained in good yields by subsequent treatment with different electrophiles. © The Royal Society of Chemistry 2013.
Persistent Identifierhttp://hdl.handle.net/10722/219719
ISSN
2015 Impact Factor: 6.567
2015 SCImago Journal Rankings: 2.771

 

DC FieldValueLanguage
dc.contributor.authorXue, Fei-
dc.contributor.authorZhao, Jin-
dc.contributor.authorHor, T. S Andy-
dc.date.accessioned2015-09-23T02:57:48Z-
dc.date.available2015-09-23T02:57:48Z-
dc.date.issued2013-
dc.identifier.citationChemical Communications, 2013, v. 49, n. 86, p. 10121-10123-
dc.identifier.issn1359-7345-
dc.identifier.urihttp://hdl.handle.net/10722/219719-
dc.description.abstractA simple and efficient catalytic arylmagnesiation of diarylacetylenes and aryl(alkyl)acetylenes is accomplished by NiCl2·6H2O at r.t. in the absence of stabilising ligands. The corresponding tetra-substituted alkenes can be obtained in good yields by subsequent treatment with different electrophiles. © The Royal Society of Chemistry 2013.-
dc.languageeng-
dc.relation.ispartofChemical Communications-
dc.titleAmbient arylmagnesiation of alkynes catalysed by ligandless nickel(ii)-
dc.typeArticle-
dc.description.natureLink_to_subscribed_fulltext-
dc.identifier.doi10.1039/c3cc45202f-
dc.identifier.scopuseid_2-s2.0-84885091489-
dc.identifier.volume49-
dc.identifier.issue86-
dc.identifier.spage10121-
dc.identifier.epage10123-
dc.identifier.eissn1364-548X-

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