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Photoinduced Electron Transfer Oxygenations of 4-Arylmethylene-1,3(2H,4H)-Isoquinolinediones Via Their Anion Radical Intermediates

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Photoinduced Electron Transfer Oxygenations of 4-Arylmethylene-1,3(2H,4H)-isoquinolinediones afforded oxiranes (5a-5c, 6a-6c, 7) and 1, 3, 4-isoquinolinetriones (8 and 9) as major products in high yields in the presence of triethylamine (TEA). These oxygenation reactions are initiated by single electron transfer between photoexcited 4-Arylmethylene-1,3(2H,4H)-isoquinolinediones and TEA, and proceeded via the anion radicals of the substrates.

Affiliations: 1: Department of Chemistry, Nanjing University, Nanjing 210093, P. R. CHINA

10.1163/156856700X00606
/content/journals/10.1163/156856700x00606
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/content/journals/10.1163/156856700x00606
2017-11-24

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