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Biconcave and Convex–Concave Tribenzotriquinacene Dimers

机译:Biconcave和凸凹二苯并二苯胺二聚体

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摘要

A new chiral tribenzotriquinacene bearing an ortho -bromoaniline nucleus was synthesized and optically resolved. The individual enantiomers, the absolute configuration of which was confirmed by single-crystal X-ray structure analysis, were stereoselectively converted into the same pyrazine-fused syn -bis-TBTQ derivative by chirality-assisted Buchwald–Hartwig amination. The corresponding diastereomeric anti -dimer was obtained alongside the syn -dimer from the racemic sample under similar reaction conditions. X-ray structure analysis of the dimers confirmed the mutual biconcave and convex–concave configuration of their TBTQ moieties and the preservation of the orthogonal orientation of the indane wings within each of them.
机译:轴承轴承轴承的新的手性二苯并二碳茚(官核核,合成并光学分辨。 单晶X射线结构分析证实的个体对映体,通过手性辅助Buchwald-Hartwig胺化将立体选择性地转化为相同的吡嗪融合的吡嗪融合的衍生物。 在类似的反应条件下,与从外消旋样品一起获得的相应的非对映异构体抗-dimer。 二聚体的X射线结构分析证实了它们的TBTQ部分的相互双合并和凸凹构造,并保存了它们中的每一个内的吲哚翅膀的正交取向。

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  • 来源
    《The Journal of Organic Chemistry》 |2018年第7期|共8页
  • 作者单位

    State Key Laboratory of Applied Organic Chemistry and College of Chemistry and Chemical Engineering Lanzhou University Lanzhou P.R. China;

    State Key Laboratory of Applied Organic Chemistry and College of Chemistry and Chemical Engineering Lanzhou University Lanzhou P.R. China;

    State Key Laboratory of Applied Organic Chemistry and College of Chemistry and Chemical Engineering Lanzhou University Lanzhou P.R. China;

    Department of Chemistry and Center of Novel Functional Molecules The Chinese University of Hong Kong Shatin Hong Kong SAR;

    Department of Chemistry and Center for Molecular Materials (CM2) Bielefeld University 33615 Bielefeld Germany;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 有机化学;
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