Environmentally Benign Strategy for Arylation of Nitronyl Nitroxide Using a Non-Transition Metal Nucleophile

We have developed a method for the arylation of nitronyl nitroxide without using its transition metal complex as a nucleophile. Various nitronyl nitroxide-substituted π-electronic compounds can be obtained from the parent nitronyl nitroxide and the corresponding aryl iodides using a combination of z...

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Veröffentlicht in:Organic letters 2020-02, Vol.22 (4), p.1350-1354
Hauptverfasser: Suzuki, Shuichi, Nakamura, Fumiya, Naota, Takeshi
Format: Artikel
Sprache:eng
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Zusammenfassung:We have developed a method for the arylation of nitronyl nitroxide without using its transition metal complex as a nucleophile. Various nitronyl nitroxide-substituted π-electronic compounds can be obtained from the parent nitronyl nitroxide and the corresponding aryl iodides using a combination of zero-valent palladium catalysts and a 2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl ligand in the presence of sodium tert-butoxide. The utility of the method has been demonstrated by the direct synthesis of open-shell compounds with giant π-electronic systems, such as 10P.
ISSN:1523-7060
1523-7052
DOI:10.1021/acs.orglett.9b04655