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4,5-ethano-4,5-dihydropyrene | 143889-70-7

中文名称
——
中文别名
——
英文名称
4,5-ethano-4,5-dihydropyrene
英文别名
Pentacyclo[8.6.2.02,5.06,18.013,17]octadeca-1(16),6,8,10(18),11,13(17),14-heptaene
4,5-ethano-4,5-dihydropyrene化学式
CAS
143889-70-7
化学式
C18H14
mdl
——
分子量
230.309
InChiKey
KLFXQTKNPOWUSM-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):
    5.2
  • 重原子数:
    18
  • 可旋转键数:
    0
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.22
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Synthesis and properties of dihydrocyclobuta[e]pyrene and tetrahydrodicyclobuta[e,l]pyrene
    摘要:
    Dihydrocyclobuta[e]pyrene and tetrahydrodicyclobuta[e,l]pyrene were prepared by the sequence of photo-cycloaddition of stryene derivatives, transannulation, and aromatization through lithiation. They reacted with dienophiles at 180-degrees-C to afford Diels-Alder adducts in excellent yields.
    DOI:
    10.1021/jo00048a031
  • 作为产物:
    描述:
    4,5-ethano-4,5,9,10-tetrahydropyrene 在 2,3-二氯-5,6-二氰基-1,4-苯醌 作用下, 以 为溶剂, 反应 3.0h, 以87%的产率得到4,5-ethano-4,5-dihydropyrene
    参考文献:
    名称:
    Synthesis and properties of dihydrocyclobuta[e]pyrene and tetrahydrodicyclobuta[e,l]pyrene
    摘要:
    Dihydrocyclobuta[e]pyrene and tetrahydrodicyclobuta[e,l]pyrene were prepared by the sequence of photo-cycloaddition of stryene derivatives, transannulation, and aromatization through lithiation. They reacted with dienophiles at 180-degrees-C to afford Diels-Alder adducts in excellent yields.
    DOI:
    10.1021/jo00048a031
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文献信息

  • Synthesis and properties of dihydrocyclobuta[e]pyrene and tetrahydrodicyclobuta[e,l]pyrene
    作者:Yasuhiro Wada、Tetsuya Tago、Katsuyuki Sugata、Jun Nishimura
    DOI:10.1021/jo00048a031
    日期:1992.10
    Dihydrocyclobuta[e]pyrene and tetrahydrodicyclobuta[e,l]pyrene were prepared by the sequence of photo-cycloaddition of stryene derivatives, transannulation, and aromatization through lithiation. They reacted with dienophiles at 180-degrees-C to afford Diels-Alder adducts in excellent yields.
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