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3,3'-di-phenanthren-9-yl-biphenyl-2,2'-diol

中文名称
——
中文别名
——
英文名称
3,3'-di-phenanthren-9-yl-biphenyl-2,2'-diol
英文别名
3,3'-di-9-phenanthryl biphenyl-2,2'-diol;2-(2-Hydroxy-3-phenanthren-9-ylphenyl)-6-phenanthren-9-ylphenol
3,3'-di-phenanthren-9-yl-biphenyl-2,2'-diol化学式
CAS
——
化学式
C40H26O2
mdl
——
分子量
538.645
InChiKey
FSCIRSDDUJIKKD-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    11.1
  • 重原子数:
    42
  • 可旋转键数:
    3
  • 环数:
    8.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    40.5
  • 氢给体数:
    2
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    3,3'-di-phenanthren-9-yl-biphenyl-2,2'-diol吡啶三氯氧磷 作用下, 以82 %的产率得到6-hydroxy-4,8-di(phenanthren-9-yl)dibenzo[d,f][1,3,2]dioxaphosphepine 6-oxide
    参考文献:
    名称:
    α-取代环酮的直接区域选择性脱氢
    摘要:
    描述了在 2,3-二氯苯并-5,6-二氰基-1,4-苯醌存在下,α-取代环酮的高度区域选择性一步脱氢。该反应通过基于磷酸的烯醇催化进行,并提供多种 α-芳基和 α-烷基取代的 α,β-不饱和酮。
    DOI:
    10.1002/anie.202307081
  • 作为产物:
    描述:
    9-溴菲盐酸正丁基锂 作用下, 以 四氢呋喃甲醇正己烷二氯甲烷 为溶剂, 反应 99.0h, 生成 3,3'-di-phenanthren-9-yl-biphenyl-2,2'-diol
    参考文献:
    名称:
    Macroscopic Expression of the Chirality of Amino Alcohols by a Double Amplification Mechanism in Liquid Crystalline Media
    摘要:
    The central chirality of simple amino alcohols was amplified by binding to a dynamically axially chiral biphenol receptor and expressed as supramolecular chirality by effecting a change from a nematic to a cholesteric liquid crystalline phase.
    DOI:
    10.1021/ja054352n
  • 作为试剂:
    描述:
    氰基甲酸乙酯2-biphenyl-4-ylmethylene-malonic acid diethyl ester3,3'-di-phenanthren-9-yl-biphenyl-2,2'-dioltitanium(IV) isopropylate9-表-辛可宁异丙醇 作用下, 反应 72.5h, 以99%的产率得到ethyl 2-carbethoxy-3-cyano-3-(4-biphenyl)propionate
    参考文献:
    名称:
    Asymmetric Cyanation of Activated Olefins with Ethyl Cyanoformate Catalyzed by a Modular Titanium Catalyst
    摘要:
    Asymmetric cyanation of a class of easily available olefins with a favorable cyanide source ethyl cyanoformate (CNCOOEt) was realized by an interesting modular catalyst. High yields and ee values were obtained for a range of substrates under solvent-free and mild reaction conditions. The products obtained could be easily transformed to the enantioenriched useful intermediates 5, 6, and pharmaceutically important gamma-aminobutyric acid 7.
    DOI:
    10.1021/ol100169r
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文献信息

  • Macroscopic Expression of the Chirality of Amino Alcohols by a Double Amplification Mechanism in Liquid Crystalline Media
    作者:Rienk Eelkema、Ben L. Feringa
    DOI:10.1021/ja054352n
    日期:2005.10.1
    The central chirality of simple amino alcohols was amplified by binding to a dynamically axially chiral biphenol receptor and expressed as supramolecular chirality by effecting a change from a nematic to a cholesteric liquid crystalline phase.
  • Direct Regioselective Dehydrogenation of α‐Substituted Cyclic Ketones
    作者:Sebastian Armin Schwengers、Gabriela Guillermina Gerosa、Tynchtyk Amatov、Naoki Yasukawa、Sebastian Brunen、Markus Leutzsch、Benjamin Mitschke、Grigory André Shevchenko、Benjamin List
    DOI:10.1002/anie.202307081
    日期:2023.8.28
    A highly regioselective, one-step dehydrogenation of α-substituted cyclic ketones in the presence of 2,3-dichlorobenzo-5,6-dicyano-1,4-benzoquinone is described. The reaction proceeds via phosphoric acid-based enol catalysis and provides access to several α-aryl and α-alkyl substituted α,β-unsaturated ketones.
    描述了在 2,3-二氯苯并-5,6-二氰基-1,4-苯醌存在下,α-取代环酮的高度区域选择性一步脱氢。该反应通过基于磷酸的烯醇催化进行,并提供多种 α-芳基和 α-烷基取代的 α,β-不饱和酮。
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