首页> 外文期刊>The Journal of Organic Chemistry >Reaction of polyhaloalkyl-substituted chromones, pyrones, and furanones with salicylaldehydes as a direct route to fused 2H-chromenes
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Reaction of polyhaloalkyl-substituted chromones, pyrones, and furanones with salicylaldehydes as a direct route to fused 2H-chromenes

机译:聚卤代烷基取代的色酮,吡喃酮和呋喃酮与水杨醛的反应是直接合成2H-色烯的途径

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摘要

Polyhaloalkyl-substituted chromones, gamma-pyrones, and beta-furanones react with salicylaldehydes in the presence of piperidine to give a wide variety of fused 2H-chromenes in good yields. This novel annulation reaction presumably proceeds by a tandem intermolecular oxa-Michael addition and subsequent intramolecular Mannich condensation.
机译:在哌啶存在下,多卤代烷基取代的色酮,γ-吡喃酮和β-呋喃酮与水杨醛反应,以高收率得到各种稠合的2H-色烯。这种新颖的环化反应大概是通过串联分子间的氧杂-迈克尔加成反应以及随后的分子内曼尼希缩合进行的。

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