Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12779/6581
DC FieldValueLanguage
dc.contributor.authorBianchi, Laraen_us
dc.contributor.authorGiorgi, Gianlucaen_us
dc.contributor.authorMaccagno, Massimoen_us
dc.contributor.authorPetrillo, Giovannien_us
dc.contributor.authorScapolla, Carloen_us
dc.contributor.authorTavani, Cinziaen_us
dc.date.accessioned2021-03-30T16:04:19Z-
dc.date.available2021-03-30T16:04:19Z-
dc.date.issued2016-
dc.identifier.issn0040-4020en_US
dc.identifier.urihttp://hdl.handle.net/20.500.12779/6581-
dc.description206126en_US
dc.language.isoenen_US
dc.relationNoneen_US
dc.relation.ispartofTETRAHEDRONen_US
dc.subjectMichael additions; Nitrobutadienes; Nitrogen heterocycles; Pyrroles; Vinylic nucleophilic substitutions; Biochemistry; Drug Discovery3003 Pharmaceutical Science; Organic Chemistryen_US
dc.titleOn the behavior of bis(sulfonyl)nitrobutadienes towards primary amines: a convenient access to 1-alkyl-2-aryl-4-(phenylsulfonyl)pyrrolesen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.tet.2016.09.044en_US
dc.identifier.scopus2-s2.0-84990866278en_US
dc.identifier.isiWOS:000386404600020en_US
dc.identifier.urlhttp://www.journals.elsevier.com/tetrahedron/en_US
dc.relation.volume72en_US
dc.relation.issue44en_US
dc.description.firstpage7050en_US
dc.description.lastpage7058en_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.orcid0000-0002-8817-7745-
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