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dc.contributor.authorWen, Min-
dc.contributor.authorErb, William-
dc.contributor.authorMongin, Florence-
dc.contributor.authorHalauko, Yury S.-
dc.contributor.authorIvashkevich, Oleg A.-
dc.contributor.authorMatulis, Vadim E.-
dc.contributor.authorRoisnel, Thierry-
dc.contributor.authorDorcet, Vincent-
dc.date.accessioned2022-11-17T11:16:32Z-
dc.date.available2022-11-17T11:16:32Z-
dc.date.issued2021-
dc.identifier.citationOrganometallics 2021;40(8):1129-1147.ru
dc.identifier.urihttps://elib.bsu.by/handle/123456789/289407-
dc.description.abstractDespite the well-established pharmacological properties of aromatic sulfonamides and the interest of introducing ferrocene into drugs, ferrocene sulfonamides have scarcely been studied. General synthetic methods using lithium bases to perform sulfonamide-directed deprotolithiation or the "halogen dance"reaction are here reported for the functionalization of N,N-dialkylferrocenesulfonamides toward various polysubstituted derivatives. Postfunctionalization of the ferrocenyl iodides by cross-coupling and lithium/iodine exchange reactions were also considered. Finally, the ligand behavior of new ferrocene phosphines in palladium-catalyzed coupling reactions was studied, and the reaction outcomes are viewed in light of DFT calculations.ru
dc.description.sponsorshipThis work was supported by the Agence Nationale de la Recherche (Ferrodance project) and the Université de Rennes 1. We also thank Rennes Métropole. We acknowledge the Fonds Européen de Développement Régional (FEDER; D8 VENTURE Bruker AXS diffractometer) and Thermofisher (generous gift of 2,2,6,6-tetramethylpiperidine). Dedicated to Professor Victor Snieckus in recognition of his stimulating work on ortho-deprotometalation and ferrocene functionalization.ru
dc.language.isoenru
dc.publisherAmerican Chemical Societyru
dc.rightsinfo:eu-repo/semantics/openAccessru
dc.subjectЭБ БГУ::ЕСТЕСТВЕННЫЕ И ТОЧНЫЕ НАУКИ::Физикаru
dc.subjectЭБ БГУ::ЕСТЕСТВЕННЫЕ И ТОЧНЫЕ НАУКИ::Химияru
dc.titleFunctionalization of N, N-Dialkylferrocenesulfonamides toward Substituted Derivativesru
dc.typearticleru
dc.rights.licenseCC BY 4.0ru
dc.identifier.DOI10.1021/acs.organomet.1c00091-
dc.identifier.scopus85105084708-
Располагается в коллекциях:Статьи сотрудников НИИ ФХП

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