2018
DOI: 10.1002/bkcs.11530
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Photocatalyst‐free Photoredox Arylation of Quinoxalin‐2(1H)‐Ones with Aryldiazo Sulfones

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Cited by 30 publications
(13 citation statements)
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“…As part of the research program investigating the redox reactions of aromatics and alkene derivatives, 5k‐5s,9 we recently reported the radical‐mediated functionalization of aromatics and alkenes by anodic oxidation 10 . In this communications, we wish to report the electrochemical oxidative arylsulfonylation/1,2‐alkyl shift sequences of alkenyl cyclobutanols.…”
Section: Methodsmentioning
confidence: 99%
“…As part of the research program investigating the redox reactions of aromatics and alkene derivatives, 5k‐5s,9 we recently reported the radical‐mediated functionalization of aromatics and alkenes by anodic oxidation 10 . In this communications, we wish to report the electrochemical oxidative arylsulfonylation/1,2‐alkyl shift sequences of alkenyl cyclobutanols.…”
Section: Methodsmentioning
confidence: 99%
“…近年来, 特别是 3 位取代喹喔啉酮 吸引人们的广泛合成兴趣 [24] . 2018 年, Kim 教授课题 组 [25] 发展了可见光诱导下芳基偶氮砜与喹喔啉酮 C(3) 2019 年, 邱頔课题组 [27] 亚砜是极有价值的含硫有机化合物, 它不仅大量存 在于天然产物和药理活性化合物中, 而且还常常用于构 建各种重要药物分子. 其传统合成方法主要依赖于硫醚 的氧化, 涉及使用金属试剂和化学计量的高价碘或过氧 化物氧化剂.…”
Section: 芳基偶氮砜参与的芳基化反应unclassified
“…In the same year, Kim and coworkers also developed successfully a photocatalyst-free photoredox arylation of quinoxalin-2(1H)-ones with aryldiazo sulfones (Scheme 16). [38] The reaction was completed without any other metal, oxidant, or additives. The proposal protocol was a facile way for the synthesis of 3-arylquinoxalin-2(1H)-one derivatives with a wide range of functional group tolerance.…”
Section: Scheme 15 Visible-light-induced 3-arylation Of Quinoxalin-2(1h)-ones With Aryl Diazonium Saltsmentioning
confidence: 99%