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 |
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Hauptverfasser: | , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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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. |
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ISSN: | 1477-0520 1477-0539 |
DOI: | 10.1039/d0ob00086h |