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I-2 catalyzed tandem protocol for synthesis of quinoxalines via sp(3), sp(2) and sp C-H functionalization

机译:I-2催化串联串联方案,用于通过SP(3),SP(2)和SP C-H官能化合成喹喔啉

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摘要

One-pot, atom-economic synthesis of quinoxalines has been achieved through generation of arylglyoxal from easily available ethylarenes, ethylenearenes and ethynearenes, and subsequent condensation with o-phenylenediamines. Catalytic I-2 with TBHP as an oxidant in DMSO is the system of choice for this domino reaction involving C-H functionalization/oxidative cyclization. This metal-free, mechanistically distinct and functional group tolerant tandem approach could be a powerful complement to traditional approaches for the synthesis of quinoxalines.
机译:通过从易于获得的乙烯基,乙烯烯烯烯烃,乙烯烯烃,乙基烯酮和乙炔化的芳基甘油甘油甘油甘油氧,以及随后用O-苯二胺的缩合来实现喹喔啉的一锅。 具有TBHP作为DMSO中氧化剂的催化I-2是该多米诺反应的选择系统,涉及C-H官能化/氧化环化。 这种无金属,机械主义鲜明和官能团的耐受性串联方法可能是对合成喹喔啉的传统方法的强大补充。

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