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A novel C–C radical–radical coupling reaction promoted by visible light: facile synthesis of 6-substituted N-methyl 5,6-dihydrobenzophenanthridine alkaloids

机译:通过可见光促进的新型C-C自由基偶联反应:容易合成6-取代的N-甲基5,6-二羟基苯蒽蒽生物碱

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A novel photoredox-mediated direct intermolecular C–H functionalization of N -methyl 5,6-dihydrobenzophenanthridine is developed utilizing the visible light-induced reductive quenching pathway of photocatalyst Ir(ppy) _(3) . In the proposed coupling mechanism, an α-amino C-radical is generated at the 6-position of N -methyl 5,6-dihydrobenzophenanthridine which is capable of coupling with α-EWG (electron withdrawing group) substituted C-radicals. The utility of this methodology has been demonstrated via rapid access to the analogue of natural 6-substituted N -methyl 5,6-dihydrobenzophenanthridine alkaloids.
机译:使用可见光诱导的光催化剂IR(PPY)_(3)的可见光诱导的还原猝灭途径开发了一种新型的光致毒介导的N-二氢苯蒽蒽醌的直肠分子间C-H官能化。在所提出的偶联机构中,在α-氨基C-基团的α-氨基C-基团处产生,其能够与α-EWG(电子取出基团)取代的C-基团偶联。通过快速进入自然6取代的N-二甲基蒽蒽生物碱的类似物质的快速进入来证明该方法的效用。

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