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3,7-exo-syn-Hexacyclo<12.2.1.12,8.19,12.03,7.011,15>nonadeca-1(17),5,9(18)-triene-4,10,16-trione | 136984-01-5

中文名称
——
中文别名
——
英文名称
3,7-exo-syn-Hexacyclo<12.2.1.12,8.19,12.03,7.011,15>nonadeca-1(17),5,9(18)-triene-4,10,16-trione
英文别名
3,7-exo-syn-Hexacyclo<12.2.1.12,8.19,12.03,7.011,15>nonadeca-1(17),5,9(18)-triene-4,10,16-trione;3,7-exo-syn-Hexacyclo[12.2.1.12,8.19,12.03,7.011,15]nonadeca-1(17),5,9(18)-triene-4,10,16-trione
3,7-exo-syn-Hexacyclo<12.2.1.12,8.19,12.03,7.011,15>nonadeca-1(17),5,9(18)-triene-4,10,16-trione化学式
CAS
136984-01-5
化学式
C19H16O3
mdl
——
分子量
292.334
InChiKey
ODSMPUOXCLAOKL-UZHYYUPUSA-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):
    1.89
  • 重原子数:
    22.0
  • 可旋转键数:
    0.0
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.53
  • 拓扑面积:
    51.21
  • 氢给体数:
    0.0
  • 氢受体数:
    3.0

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    13,17-exo-syn-Octacyclo<10.5.1.15,8.02,6.02,11.04,9.07,11.013,17>nonadec-15-ene-3,10,14-trione 650.0 ℃ 、26.66 Pa 条件下, 以36%的产率得到3,7-exo-syn-Hexacyclo<12.2.1.12,8.19,12.03,7.011,15>nonadeca-1(17),5,9(18)-triene-4,10,16-trione
    参考文献:
    名称:
    Roofed polyquinanes: synthesis and electronic structure
    摘要:
    Starting from readily available norbornenobenzoquinone 7 and employing a photothermal metathesis reaction as the main strategy, novel "roofed" polyquinane bisenones 3 and 13 have been synthesized. Among these, the former is potentially serviceable for further elaboration to dodecahedrane 1. Catalytic hydrogenation of 3 provided the dione 12, which fully inscribes the circumference of dodecahedrane sphere. The "roofed" C-16-bisenone 3 has been successfully annulated to C19-bisenone 24 and C19-trisenone 26 by employing the Greene methodology and Pauson-Khand reaction, respectively. The molecular structures of 3 and 13 were computed using molecular mechanics and semiempirical MO methods. The nonbonded distances between the double bonds vary strongly with the method employed. The interactions between the pi-MO's were, therefore, probed by means of photoelectron (PE) spectroscopy. Comparison with the PE spectra of a series of model systems with increasing complexity enabled an unambiguous assignment of the observed peaks. The symmetric and antisymmetric combinations of the pi-MO's of the enone moieties of 3 and 13 show large splittings, characteristic of propano-bridged systems in which through-space and through-bond effects act in concert.
    DOI:
    10.1021/jo00025a019
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