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Authordc.contributor.authorGrau, Fanny 
Authordc.contributor.authorBayón, J. 
Authordc.contributor.authorAguirre, Pedro 
Authordc.contributor.authorParella, Teodor 
Authordc.contributor.authorDuñach, Elisabet 
Admission datedc.date.accessioned2018-12-20T15:10:04Z
Available datedc.date.available2018-12-20T15:10:04Z
Publication datedc.date.issued2008
Cita de ítemdc.identifier.citationEur. J. Org. Chem. 2008, 1214–1223
Identifierdc.identifier.issn1434193X
Identifierdc.identifier.issn10990690
Identifierdc.identifier.other10.1002/ejoc.200700881
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/158128
Abstractdc.description.abstractThe Rh-catalysed hydroformylation of isopropylidenecyclohexane derivatives obtained by intramolecular diene cyclisations affords the corresponding aldehydes in good yields and in a completely chemo- and regioselective manner. Diastereoselectivities of ca. 90%were achieved for all substrates when a bulky phosphite was used as the Rh ligand. The stereochemical outcomes of the hydroformylation reactions were established by detailed NMR studies. The olfactory evaluation of the different aldehydes is also presented.
Lenguagedc.language.isoen
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
Sourcedc.sourceEuropean Journal of Organic Chemistry
Keywordsdc.subjectAldehydes
Keywordsdc.subjectHydroformylation
Keywordsdc.subjectIsopropylidenecyclohexane
Keywordsdc.subjectNMR spectroscopy
Keywordsdc.subjectStereochemistry
Títulodc.titleNew aldehydes by catalytic diene cycloisomerisations
Document typedc.typeArtículo de revista
Catalogueruchile.catalogadorrvh
Indexationuchile.indexArtículo de publicación SCOPUS
uchile.cosechauchile.cosechaSI


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Attribution-NonCommercial-NoDerivs 3.0 Chile
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Chile