Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/107440
DC FieldValueLanguage
dc.contributor.authorBrandão, Pedro-
dc.contributor.authorMarques, Carolina S.-
dc.contributor.authorCarreiro, Elisabete P.-
dc.contributor.authorPineiro, Marta-
dc.contributor.authorBurke, Anthony J.-
dc.date.accessioned2023-07-12T09:18:02Z-
dc.date.available2023-07-12T09:18:02Z-
dc.date.issued2021-04-
dc.identifier.issn1527-8999pt
dc.identifier.issn1528-0691pt
dc.identifier.urihttps://hdl.handle.net/10316/107440-
dc.description.abstractMulticomponent reactions (MCRs) are a valuable tool in diversity-oriented synthesis. Its application to privileged structures is gaining relevance in the fields of organic and medicinal chemistry. Isatin, due to its unique reactivity, can undergo different MCRs, affording multiple interesting scaffolds, namely oxindole-derivatives (including spirooxindoles, bis-oxindoles and 3,3-disubstituted oxindoles) and even, under certain conditions, ring-opening reactions occur that leads to other heterocyclic compounds. Over the past few years, new methodologies have been described for the application of this important and easily available starting material in MCRs. In this review, we explore these novelties, displaying them according to the structure of the final products obtained.pt
dc.language.isoengpt
dc.publisherWiley Online Librarypt
dc.relationinfo:eu-repo/grantAgreement/FCT/POR_CENTRO/PD/BD/128490/2017/PT/Sustainable Asymmetric Catalytic Synthesis of Novel Oxindole Hybrids with Potential Biological Activitypt
dc.relationinfo:eu-repo/grantAgreement/FCT/UIDB/00313/2020pt
dc.relationinfo:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDB/50006/2020/PT/Associated Laboratory for Green Chemistry - Clean Technologies and Processespt
dc.rightsembargoedAccesspt
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/pt
dc.subjectisatinpt
dc.subjectmulticomponent reactionspt
dc.subjectspiroxindolespt
dc.subjectbis-oxindolespt
dc.subject3,3-disubstituted oxindolespt
dc.subjectoxindolept
dc.subjectsustainabilitypt
dc.subjectcatalysispt
dc.subjectnanocatalystspt
dc.subjectdiversity oriented synthesispt
dc.titleEngaging Isatins in Multicomponent Reactions (MCRs) - Easy Access to Structural Diversitypt
dc.typearticle-
degois.publication.firstPage924pt
degois.publication.lastPage1037pt
degois.publication.issue4pt
degois.publication.titleThe Chemical Recordpt
dc.peerreviewedyespt
dc.identifier.doi10.1002/tcr.202000167pt
degois.publication.volume21pt
dc.date.embargo2022-04-01*
uc.date.periodoEmbargo365pt
item.cerifentitytypePublications-
item.languageiso639-1en-
item.fulltextCom Texto completo-
item.grantfulltextopen-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypearticle-
crisitem.author.researchunitCQC - Coimbra Chemistry Centre-
crisitem.author.researchunitCQC - Coimbra Chemistry Centre-
crisitem.author.parentresearchunitFaculty of Sciences and Technology-
crisitem.author.parentresearchunitFaculty of Sciences and Technology-
crisitem.author.orcid0000-0002-1455-7470-
crisitem.author.orcid0000-0002-7460-3758-
Appears in Collections:I&D CQC - Artigos em Revistas Internacionais
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