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Authordc.contributor.authorGuimet, Eugeni 
Authordc.contributor.authorParada Aliste, José es_CL
Authordc.contributor.authorDiéguez, Montserrat es_CL
Authordc.contributor.authorRuiz, Aurora es_CL
Authordc.contributor.authorClaver, Carmen es_CL
Admission datedc.date.accessioned2007-05-17T14:56:16Z
Available datedc.date.available2007-05-17T14:56:16Z
Publication datedc.date.issued2005-03-30
Cita de ítemdc.identifier.citationAPPLIED CATALYSIS A-GENERAL 282 (1-2): 215-220 MAR 30 2005en
Identifierdc.identifier.issn0926-860X
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/120408
Abstractdc.description.abstractDiphosphinite ligands 2 and 3, easily prepared from inexpensive D(+)-xylose in few steps, were tested in the Rh-catalyzed asymmetric hydroformylation of several vinyl arenes. High regio-selectivities in branched aldehyde (up to 99%) and moderate enantio-selectivity (up to 63%) were found (20-40 degrees C, 30-60 bar of syn gas). For the first time, the structure in solution of the species formed under hydroformylation conditions with diphosphinite ligands was determineden
Lenguagedc.language.isoenen
Keywordsdc.subjectENANTIOSELECTIVE HYDROFORMYLATIONen
Títulodc.titleAsymmetric hydroformylation of vinyl arenes catalyzed by furanoside diphosphinites-Rh(I) complexesen
Document typedc.typeArtículo de revista


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