首页> 外文期刊>Synthesis: International Journal of Methods in Synthetic Organic Chemistry >An Expedient Synthesis of Bis-Fused Benzofuran and a Two-Directional Ring-Closing Metathesis for the Synthesis of Bisbenzoxepines and Bisbenzoxocines
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An Expedient Synthesis of Bis-Fused Benzofuran and a Two-Directional Ring-Closing Metathesis for the Synthesis of Bisbenzoxepines and Bisbenzoxocines

机译:双融合苯并呋喃的简便合成方法和双向闭合环复分解法,用于合成双苯并二氢吡啶和双苯并benzo

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摘要

Synthesis of bis-fused benzofuran derivatives by the implementation of palladium-mediated intramolecular cyclization is described. To our knowledge, this is the first report of the synthesis of bis-fused benzofuran by this protocol. Bisbenzoxepine and bis-benzoxocine derivatives were also synthesized by the application of two-directional ring-closing metathesis.As a part of our continuing study concerning the carbon-carbon bond-forming reactions utilizing the palladium-mediated intramolecular cyclization strategy, we have reported variously functionalized medium-sized hetero-cycles with a possible evaluation of the potentially bioac-tive moieties. We have also developed an important synthetic methodology for the construction of medium-sized heterocyclic compounds from the unactivated allyl-ic system via the C-H activation method by the application of intramolecular Heck reaction sequence.
机译:描述了通过钯介导的分子内环化的合成双稠合苯并呋喃衍生物。据我们所知,这是该方案合成双稠合苯并呋喃的首次报道。还通过应用双向闭环复分解反应合成了双苯并xepine和双苯并xoxine衍生物。作为我们关于利用钯介导的分子内环化策略进行碳-碳键形成反应的持续研究的一部分,我们进行了各种报道功能化的中型杂环,并可能评估其潜在的生物活性部分。我们还开发了一种重要的合成方法,可通过应用分子内Heck反应序列,通过C-H活化方法,从未活化的烯丙基体系构建中等尺寸的杂环化合物。

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