首页> 外文期刊>The Journal of Organic Chemistry >Iodine-Catalyzed 1,3-Dipolar Cycloaddition/Oxidation/Aromatization Cascade with Hydrogen Peroxide as the Terminal Oxidant: General Route to Pyrrolo[2,1-a]isoquinolines
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Iodine-Catalyzed 1,3-Dipolar Cycloaddition/Oxidation/Aromatization Cascade with Hydrogen Peroxide as the Terminal Oxidant: General Route to Pyrrolo[2,1-a]isoquinolines

机译:以过氧化氢为末端氧化剂的碘催化的1,3-偶极环加成/氧化/芳构化级联反应:通向吡咯并[2,1-a]异喹啉的一般路线

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摘要

We report a novel molecular iodine-catalyzed 1,3-dipolar cycloaddition/oxidation/aromatization cascade process with hydrogen peroxide as the terminal oxidant for the construction of pyrrolo[2,1-a]isoquinolines. The product pyrrolo[2,1-a]- isoquinolines were obtained from reactions between simple, readily available dipolarophiles and tetrahydroisoquinolines in moderate to excellent yields without the need for a metal catalyst.
机译:我们报告了一种新型的分子碘催化的过氧化氢作为吡咯并[2,1-a]异喹啉结构的末端氧化剂的1,3-偶极环加成/氧化/芳香化级联过程。吡咯并[2,1-a]-异喹啉产品是由简单易得的双极性亲和剂与四氢异喹啉之间的反应获得的,其收率中等至优异,而无需金属催化剂。

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