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首页> 外文期刊>Bulletin of the Korean Chemical Society >Synthesis of 3,4,5-Trisubstituted Isoxazoles through Gold-Catalyzed Cascade Cyclization−Oxidative Alkynylation and Cyclization-Fluorination of 2-Alkynone O-Methyloximes
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Synthesis of 3,4,5-Trisubstituted Isoxazoles through Gold-Catalyzed Cascade Cyclization−Oxidative Alkynylation and Cyclization-Fluorination of 2-Alkynone O-Methyloximes

机译:金催化级联环氧化-氧化炔基和2-炔酮 O -甲基肟的环化-氟合成3,4,5-三取代异恶唑

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摘要

Gold-catalyzed tandem cyclization−oxidative alkynylation and cyclization-fluorination reactions of 2- alkynone O-methyloximes are described. The reactions proceed smoothly at room temperature in the presence of 10 mol % of (PPh3)AuNTf2, 2.5 equivalents of selectfluor, and 2 equivalents of K3PO4. 2-Alkynone Omethyloximes undergo intramolecular oxyauration/cyclization and ensuing oxidative cross-coupling and fluorination process to afford the corresponding 3,4,5-trisubstituted isoxazoles in a cascade manner.
机译:描述了金催化的2-炔基O-甲基肟的串联环化-氧化炔基化和环化-氟化反应。反应在室温下在10摩尔%(PPh3)AuNTf2、2.5当量的selectfluor和2当量的K3PO4的存在下平稳进行。 2-炔酮O甲基肟经历分子内的氧修饰/环化,并随后进行氧化交叉偶联和氟化过程,从而以级联方式提供相应的3,4,5-三取代的异恶唑。

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