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首页> 外文期刊>Tetrahedron >Synthesis of 1-azaxanthones by condensation of 1,3-bis(trimethylsilyloxy)-1,3-butadienes with 3-(cyano)benzopyrylium triflates and subsequent domino 'retro-Michaelitrile-addition/heterocyclization' reaction
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Synthesis of 1-azaxanthones by condensation of 1,3-bis(trimethylsilyloxy)-1,3-butadienes with 3-(cyano)benzopyrylium triflates and subsequent domino 'retro-Michaelitrile-addition/heterocyclization' reaction

机译:通过1,3-双(三甲基甲硅烷氧基)-1,3-丁二烯与3-(氰基)苯并吡啶三氟甲磺酸酯的缩合反应和随后的多米诺骨牌反应(``迈克尔-还原/腈加成/杂环化''反应)合成1-氮杂蒽酮

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摘要

Functionalized 1-azaxanthones (5-oxo-5H-[1]-benzopyrano[2,3-b]pyridines) were prepared by TMSOTf-mediated condensation of 1,3-bis(trimethylsilyloxy)-1,3-butadienes with 3-cyanochromones and subsequent base-mediated domino 'retro-Michaelitrile-addition/heterocyclization' reaction. (C) 2008 Elsevier Ltd. All rights reserved.
机译:通过TMSOTf介导的1,3-双(三甲基甲硅烷氧基)-1,3-丁二烯与3-的缩合制备功能化的1-氮杂黄嘌呤(5-oxo-5H- [1]-苯并吡喃并[2,3-b]吡啶)氰基色酮和随后的碱基介导的多米诺骨牌“复古迈克尔/腈加成/杂环化”反应。 (C)2008 Elsevier Ltd.保留所有权利。

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