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Type-Itemized Enumeration of [2.2]Paracyclophane Derivatives for Recasting the Concept of Stereogenic Planes by Fujita's Stereoisogram Approach

机译:[2.2]统治统称的序列枚举,用于通过富士塔的立体图方法重铸整个立体飞机概念的衍生物

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摘要

Planar chirality of [2.2]Paracyclophane derivatives has been treated by applying Fujita's stereoisogram approach (Fujita, S. Mathematical Stereochemistry, De-Gruyter, 2015). By means of stereoisograms, three kinds of symmetries (chirality, RS-stereogenicity and sclerality) have been integrated into RS-stereoisomerism, which are classified into five types. Fujita's proligand method for 3D structure (Fujita, S. Symmetry and Combinatorial Enumeration in Chemistry, Springer-Verlag, 1991; Fujita, S. Combinatorial Enumeration of Graphs, Three-Dimensional Structures, and Chemical Compounds, University of Kragujevac, Faculty of Science: Kragujevac, 2013) has been extended to meet the requirement due to RS-stereoisomers and applied to the symmetry-itemized and type-itemized enumerations of [2.2]paracyclophane derivatives. The enumeration results are depicted by means of isomer-classification diagrams, which demonstrate isomerism of [2.2]paracyclophane derivatives.
机译:通过应用藤田的立体图方法(藤胶,S.数学立体化学,De-Gruyter,2015)来处理[2.2]截晶烷衍生物的平面手平性。 通过立体图,已经将三种对称性(手性,RS-Tereeogy和Sclerality)集成到RS-Stereoomerism中,分为五种类型。 富士塔的3D结构的贪婪方法(富士塔,S.对称和化学中的组合枚举,Springer-Verlag,1991;富士塔,S. Combinatorial枚举科学学院Kragujevac大学的图形,三维结构和化学化合物: Kragujevac,2013年)已经扩展到满足Rs-Stereoisomers引起的要求,并应用于[2.2]截谱衍生物的对称性和典型的序列。 枚举结果通过异构体分类图描绘,其示出了[2.2]截谱衍生物的异构性。

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  • 来源
    《Match》 |2019年第1期|共42页
  • 作者

    Fujita Shinsaku;

  • 作者单位

    Shonan Inst Chemoinformat &

    Math Chem Kaneko 479-7 Ooimachi Fujisawa Kanagawa 2580019 Japan;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
  • 关键词

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