Analogy of the Reactions of Aromatic and Aliphatic π-Electrophiles with Nucleophiles

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dc.contributor.authorBarbasiewicz, Michał
dc.contributor.authorFedoryński, Michał
dc.contributor.authorLoska, Rafał
dc.contributor.authorMąkosza, Mieczysław
dc.contributor.organizationFaculty of Chemistry, University of Warsawen
dc.contributor.organizationFaculty of Chemistry, Warsaw University of Technologyen
dc.contributor.organizationInstitute of Organic Chemistry, Polish Academy of Sciencesen
dc.date.accessioned2023-11-29T15:24:18Z
dc.date.available2023-11-29T15:24:18Z
dc.date.issued2023
dc.description.abstractThe aim of this essay is to disclose the similarity of a great variety of reactions that proceed between nucleophiles and pi-electrophiles—both aromatic and aliphatic. These reactions proceed via initial reversible addition, followed by a variety of transformations that are common for the adducts of both aliphatic and aromatic electrophiles. We hope that understanding of this analogy should help to expand the scope of the known reactions and inspire the search for new reactions that were overlooked.en
dc.identifier.citationMolecules 2023, 28(10), 4015 ; https://doi.org/10.3390/molecules28104015en
dc.identifier.doi10.3390/molecules28104015
dc.identifier.issn1420-3049
dc.identifier.urihttps://open.icm.edu.pl/handle/123456789/23234
dc.language.isoen
dc.publisherMDPIen
dc.rightsUznanie autorstwa 4.0 Międzynarodowe*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectnucleophilic substitutionen
dc.subjectnucleophilic additionen
dc.subjectnucleophilesen
dc.subjectelectrophilesen
dc.subjecteliminationen
dc.subjectnitroarenesen
dc.subjectreaction mechanismsen
dc.titleAnalogy of the Reactions of Aromatic and Aliphatic π-Electrophiles with Nucleophilesen
dc.typearticleen
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