Substituent-Determined Intramolecular Hydrogen Transfer for Photopromoted Intermolecular Cycloaddition of Anthraquinones with Aryl Olefins

The formation of intramolecular hydrogen bonds in anthraquinones makes them inert to photoinduced reactions; therefore, it is a great challenge to phototransform these compounds. Herein, we reported a formal visible-light-induced [4 + 2] cycloaddition of both 1-hydroxyanthraquinones and 1-aminoanthr...

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Veröffentlicht in:Organic letters 2023-11, Vol.25 (46), p.8308-8313
Hauptverfasser: Yang, Fanyuanhang, Lin, Ping, Xu, Biping, Gao, Yuzhen, Su, Weiping
Format: Artikel
Sprache:eng
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Zusammenfassung:The formation of intramolecular hydrogen bonds in anthraquinones makes them inert to photoinduced reactions; therefore, it is a great challenge to phototransform these compounds. Herein, we reported a formal visible-light-induced [4 + 2] cycloaddition of both 1-hydroxyanthraquinones and 1-aminoanthraquinones with olefins under external photocatalyst-free conditions with high regioselectivity. More than 60 substrates are disclosed, demonstrating the reliability of this protocol to construct diverse functionalized anthraquinone derivatives.
ISSN:1523-7060
1523-7052
DOI:10.1021/acs.orglett.3c03354