Visible-light-promoted acyl radical cascade reaction for accessing acylated isoquinoline-1,3(2,4)-dione derivatives

A visible-light-promoted decarboxylative acyl radical acylation/cyclization cascade reaction of N -methacryloylbenzamides for accessing acylated isoquinoline-1,3(2 H ,4 H )-dione derivatives was described. In this report, α-keto acids were used for generating acyl radicals and inducing radical acyla...

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Veröffentlicht in:Organic & biomolecular chemistry 2020-03, Vol.18 (1), p.194-1948
Hauptverfasser: Su, Yingpeng, Zhang, Rong, Xue, Wenxuan, Liu, Xuan, Zhao, Yanan, Wang, Ke-Hu, Huang, Danfeng, Huo, Congde, Hu, Yulai
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Sprache:eng
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Zusammenfassung:A visible-light-promoted decarboxylative acyl radical acylation/cyclization cascade reaction of N -methacryloylbenzamides for accessing acylated isoquinoline-1,3(2 H ,4 H )-dione derivatives was described. In this report, α-keto acids were used for generating acyl radicals and inducing radical acylations. This protocol features mild reaction conditions, operational practicality and a broad substrate scope. A visible-light-promoted radical acylation/cyclization cascade reaction of N -methacryloylbenzamides with α-keto acids was developed to construct acylated isoquinoline-dione derivatives.
ISSN:1477-0520
1477-0539
DOI:10.1039/d0ob00086h