Engaging Isatins in Multicomponent Reactions (MCRs) – Easy Access to Structural Diversity

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.accessioned2022-03-23T16:16:40Z
dc.date.available2022-03-23T16:16:40Z
dc.date.issued2021-02-14
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.por
dc.identifier.authoremailnd
dc.identifier.authoremailcarolsmarq@uevora.pt
dc.identifier.authoremailbetepc@uevora.pt
dc.identifier.authoremailnd
dc.identifier.authoremailajb@uevora.pt
dc.identifier.doi10.1002/tcr.202000167por
dc.identifier.scientificarea307por
dc.identifier.urihttps://onlinelibrary.wiley.com/doi/10.1002/tcr.202000167
dc.identifier.urihttp://hdl.handle.net/10174/31433
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherThe Chemical Society of Japan & Wiley-VCH GmbHpor
dc.rightsopenAccesspor
dc.subjectisatinpor
dc.subjectspirooxindolespor
dc.subjectmulticomponent reactionspor
dc.subjectsustainabilitypor
dc.subjectcatalysispor
dc.subjectoxindolepor
dc.titleEngaging Isatins in Multicomponent Reactions (MCRs) – Easy Access to Structural Diversitypor
dc.typearticle

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