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Please use this identifier to cite or link to this item: https://elib.bsu.by/handle/123456789/289407
Title: Functionalization of N, N-Dialkylferrocenesulfonamides toward Substituted Derivatives
Authors: Wen, Min
Erb, William
Mongin, Florence
Halauko, Yury S.
Ivashkevich, Oleg A.
Matulis, Vadim E.
Roisnel, Thierry
Dorcet, Vincent
Keywords: ЭБ БГУ::ЕСТЕСТВЕННЫЕ И ТОЧНЫЕ НАУКИ::Физика
ЭБ БГУ::ЕСТЕСТВЕННЫЕ И ТОЧНЫЕ НАУКИ::Химия
Issue Date: 2021
Publisher: American Chemical Society
Citation: Organometallics 2021;40(8):1129-1147.
Abstract: Despite 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.
URI: https://elib.bsu.by/handle/123456789/289407
DOI: 10.1021/acs.organomet.1c00091
Scopus: 85105084708
Sponsorship: This 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.
Licence: info:eu-repo/semantics/openAccess
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