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Base-catalyzed bicyclization of dialkyl glutaconates with cinnamoylacetamides: a synthetic strategy for isoquinolinedione derivatives

机译:肉桂酸乙酰胺对谷氨酸二烷基酯的碱催化双环化:异喹啉二酮衍生物的合成策略

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摘要

We report here that polysubstituted dihydroisoquinolones and isoquinotones can be constructed by the one-pot reaction of the readily available acyclic α,β-unsaturated carbonyl precursors and dialkyl glutaconates under mild basic conditions (1-45 min for the former vs. 1-6 h for the latter) via the domino process involving [3+3] annulation/intramolecular aza-cyclization.
机译:我们在这里报告说,在温和的碱性条件下(前者为1-45分钟,而前者为1-6小时),可通过一锅反应容易获得的无环α,β-不饱和羰基前体和戊二酸二烷基酯来构建多取代的二氢异喹啉酮和异喹啉酮。后者)通过涉及[3 + 3]环空/分子内氮杂环化的多米诺骨工艺。

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  • 来源
    《Chemical Communications》 |2014年第49期|6458-6460|共3页
  • 作者单位

    Department of Chemistry, Northeast Normal University, Changchun, 130024, P. R. China;

    Department of Chemistry, Northeast Normal University, Changchun, 130024, P. R. China;

    Department of Chemistry, Northeast Normal University, Changchun, 130024, P. R. China;

    Department of Chemistry, Northeast Normal University, Changchun, 130024, P. R. China;

    Department of Chemistry, Northeast Normal University, Changchun, 130024, P. R. China;

    Department of Chemistry, Northeast Normal University, Changchun, 130024, P. R. China;

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  • 入库时间 2022-08-17 13:15:53

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