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1-[[4-[4-[(3-Formylindol-1-yl)methyl]phenyl]phenyl]methyl]indole-3-carbaldehyde | 754991-00-9

中文名称
——
中文别名
——
英文名称
1-[[4-[4-[(3-Formylindol-1-yl)methyl]phenyl]phenyl]methyl]indole-3-carbaldehyde
英文别名
1-[[4-[4-[(3-formylindol-1-yl)methyl]phenyl]phenyl]methyl]indole-3-carbaldehyde
1-[[4-[4-[(3-Formylindol-1-yl)methyl]phenyl]phenyl]methyl]indole-3-carbaldehyde化学式
CAS
754991-00-9
化学式
C32H24N2O2
mdl
——
分子量
468.555
InChiKey
JWJHIVWDXZIEGT-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):
    5.8
  • 重原子数:
    36
  • 可旋转键数:
    7
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.06
  • 拓扑面积:
    44
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    1-[[4-[4-[(3-Formylindol-1-yl)methyl]phenyl]phenyl]methyl]indole-3-carbaldehyde四氯化钛 作用下, 以 四氢呋喃 为溶剂, 以18%的产率得到7,24,35,52-tetrazatridecacyclo[52.2.2.22,5.226,29.230,33.17,14.117,24.135,42.145,52.08,13.018,23.036,41.046,51]octahexaconta-1(57),2(68),3,5(67),8,10,12,14(66),15,17(65),18,20,22,26,28,30(62),31,33(61),36,38,40,42(60),43,45(59),46,48,50,54(58),55,63-triacontaene
    参考文献:
    名称:
    Synthesis, complexation studies and biological applications of some novel stilbenophanes, indolophanes and bisindolostilbenophanes via McMurry coupling
    摘要:
    Various types of stilbenophanes, indolophanes and bisindolostilbenophanes were synthesized by intra-, inter- and tandem intra-, intermolecular McMurry coupling. Some of the indolophanes and bisindolostilbenophanes exhibited significant activity against the growth of various bacteria. Complexation of some of the cyclophanes with TCNQ has also been studied. (c) 2006 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2006.09.078
  • 作为产物:
    参考文献:
    名称:
    The use of McMurry coupling for the synthesis of indolophanes and cis-stilbenophanes
    摘要:
    Treatment of 2 equiv of indole-3-aidehyde with o, m, p-xylyl, 2,5-dimethoxy-p-xylyl dibromides and 4,4'-bis(bromomethyl)-1,1'-biphenyl gave the bisalkylated products, which underwent McMurry coupling with low valent titanium to give indolophanes. Various cis-stilbenophanes with m-terphenyl building blocks were also synthesized by application of the McMurry coupling technique. (C) 2004 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2004.06.020
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文献信息

  • The use of McMurry coupling for the synthesis of indolophanes and cis-stilbenophanes
    作者:Perumal Rajakumar、Merikapudi Gayatri Swaroop
    DOI:10.1016/j.tetlet.2004.06.020
    日期:2004.8
    Treatment of 2 equiv of indole-3-aidehyde with o, m, p-xylyl, 2,5-dimethoxy-p-xylyl dibromides and 4,4'-bis(bromomethyl)-1,1'-biphenyl gave the bisalkylated products, which underwent McMurry coupling with low valent titanium to give indolophanes. Various cis-stilbenophanes with m-terphenyl building blocks were also synthesized by application of the McMurry coupling technique. (C) 2004 Elsevier Ltd. All rights reserved.
  • Synthesis, complexation studies and biological applications of some novel stilbenophanes, indolophanes and bisindolostilbenophanes via McMurry coupling
    作者:Perumal Rajakumar、Merikapudi Gayatri Swaroop、S. Jayavelu、K. Murugesan
    DOI:10.1016/j.tet.2006.09.078
    日期:2006.12
    Various types of stilbenophanes, indolophanes and bisindolostilbenophanes were synthesized by intra-, inter- and tandem intra-, intermolecular McMurry coupling. Some of the indolophanes and bisindolostilbenophanes exhibited significant activity against the growth of various bacteria. Complexation of some of the cyclophanes with TCNQ has also been studied. (c) 2006 Elsevier Ltd. All rights reserved.
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