Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12779/3701
DC FieldValueLanguage
dc.contributor.authorGaggelli, Elenaen_us
dc.contributor.authorMarchettini, Nadiaen_us
dc.contributor.authorValensin, Giannien_us
dc.date.accessioned2021-03-30T14:35:21Z-
dc.date.available2021-03-30T14:35:21Z-
dc.date.issued1987-
dc.identifier.issn0749-1581en_US
dc.identifier.urihttp://hdl.handle.net/20.500.12779/3701-
dc.description50100en_US
dc.description.abstract13C and 1H NMR parameters were measured for isoproterenol in solution. Spin-lattice relaxation rates were considered and C-H and H-H J couplings were determined. The t rotamer was shown to occur in a much greater abundance than the two g rotamers. Dynamics in solution were interpreted in terms of a nearly isotropic motion of the α-hydroxyphenethyl moiety and of a high degree of flexibility of the isopropyl moiety, Relevant distances and dipolar connectivities were measured and used to build up a Dreiding model of the most probable conformation.en_US
dc.language.isoenen_US
dc.relationNoneen_US
dc.relation.ispartofMAGNETIC RESONANCE IN CHEMISTRYen_US
dc.title1H and 13C NMR conformational analysis in solution of isoproterenol a pure β-agonist drugen_US
dc.typeArticleen_US
dc.identifier.doi10.1002/mrc.1260251109en_US
dc.identifier.scopus2-s2.0-84989625506en_US
dc.identifier.isiWOS:A1987K958100008en_US
dc.relation.volume25en_US
dc.relation.issue11en_US
dc.description.firstpage970en_US
dc.description.lastpage974en_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.orcid9810-
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