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Article: 1,1′-P/O-ferrocenyl ligands in palladium-catalyzed Suzuki coupling of aryl chlorides

Title1,1′-P/O-ferrocenyl ligands in palladium-catalyzed Suzuki coupling of aryl chlorides
Authors
Issue Date2006
Citation
Organometallics, 2006, v. 25, n. 5, p. 1199-1205 How to Cite?
AbstractSeveral new P/O-functionalized ferrocenyl ligands have been synthesized. They react with Pd2(dba)3 to promote the Suzuki cross-couplings of a range of arylboronic acids and aryl chlorides to give the desired biaryl products in high isolated yields. Different oxidative addition products were isolated and crystallographically identified. Their roles in the catalytic pathways are discussed. © 2006 American Chemical Society.
Persistent Identifierhttp://hdl.handle.net/10722/219505
ISSN
2021 Impact Factor: 3.837
2020 SCImago Journal Rankings: 1.231
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorTeo, Shihui-
dc.contributor.authorWeng, Zhiqiang-
dc.contributor.authorHor, T. S Andy-
dc.date.accessioned2015-09-23T02:57:15Z-
dc.date.available2015-09-23T02:57:15Z-
dc.date.issued2006-
dc.identifier.citationOrganometallics, 2006, v. 25, n. 5, p. 1199-1205-
dc.identifier.issn0276-7333-
dc.identifier.urihttp://hdl.handle.net/10722/219505-
dc.description.abstractSeveral new P/O-functionalized ferrocenyl ligands have been synthesized. They react with Pd2(dba)3 to promote the Suzuki cross-couplings of a range of arylboronic acids and aryl chlorides to give the desired biaryl products in high isolated yields. Different oxidative addition products were isolated and crystallographically identified. Their roles in the catalytic pathways are discussed. © 2006 American Chemical Society.-
dc.languageeng-
dc.relation.ispartofOrganometallics-
dc.title1,1′-P/O-ferrocenyl ligands in palladium-catalyzed Suzuki coupling of aryl chlorides-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1021/om050791j-
dc.identifier.scopuseid_2-s2.0-33644899667-
dc.identifier.volume25-
dc.identifier.issue5-
dc.identifier.spage1199-
dc.identifier.epage1205-
dc.identifier.isiWOS:000235691500016-
dc.identifier.issnl0276-7333-

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