首页> 外文期刊>Bulletin of the Korean Chemical Society >Synthesis of 2,4-Diaryl-4H-Chromenes via Becarboxylative Alkylation of β-Keto Acids to ortho-Quinone Methides as Eeactive Intermediates
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Synthesis of 2,4-Diaryl-4H-Chromenes via Becarboxylative Alkylation of β-Keto Acids to ortho-Quinone Methides as Eeactive Intermediates

机译:作为邻醌甲基氨基甲基氨基甲基的二烷基化烷基化作为可重复中间体的合成2,4-二芳基-4h-铬化合物

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摘要

4H-Chromenes are ubiquitous in natural products and pharmaceuticals with a variety of physiological and biological activities.1 In particular, 2,4-diaryl-4H-chromene moiety forms the core structure of biologically active compounds such as enzyme inhibitors against a variety of targets.2
机译:4H-色度普遍存在于天然产物和药物,具有各种生理和生物学活性.1,特别是2,4-二芳基-4H-铬部分,形成生物活性化合物的核心结构,例如酶抑制剂对各种靶标 .2

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