Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12779/3542
DC FieldValueLanguage
dc.contributor.authorNesi, A.en_us
dc.contributor.authorRicci, A.en_us
dc.contributor.authorTaddei, Maurizioen_us
dc.contributor.authorTedeschi, P.en_us
dc.contributor.authorSeconi, G.en_us
dc.date.accessioned2021-03-30T14:34:22Z-
dc.date.available2021-03-30T14:34:22Z-
dc.date.issued1980-
dc.identifier.issn0022-328Xen_US
dc.identifier.urihttp://hdl.handle.net/20.500.12779/3542-
dc.description49273en_US
dc.description.abstractSeveral new organomettalic isoxazoles, silylated and stannylated in the heterocyclic ring or in a side chain have been made. Their 13C NMR spectra are consistent with the previous conclusions on the electronic effects of MR3 and CH2MR3 (M = Si, Sn) groups, and indicate the importance of the pπ-dπ and σ-π mechanisms in the various ring positionsen_US
dc.language.isoenen_US
dc.relationNoneen_US
dc.relation.ispartofJOURNAL OF ORGANOMETALLIC CHEMISTRYen_US
dc.titleGroup IVB organometallic derivatives: Synthesis and 13C NMR spectra of new silyl and stannyl isoxazolesen_US
dc.typeArticleen_US
dc.identifier.scopus2-s2.0-0001164851en_US
dc.relation.volume195en_US
dc.description.firstpage275en_US
dc.description.lastpage283en_US
dc.description.thirdmissionNot applicableen_US
item.cerifentitytypePublications-
item.grantfulltextnone-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeArticle-
item.fulltextNo Fulltext-
crisitem.author.orcid0000-0001-8660-7580-
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