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methyl 7-oxotetracyclo[4.3.2.22,5.01,6]trideca-3,8,10,12-tetraene-3-carboxylate | 131236-20-9

中文名称
——
中文别名
——
英文名称
methyl 7-oxotetracyclo[4.3.2.22,5.01,6]trideca-3,8,10,12-tetraene-3-carboxylate
英文别名
——
methyl 7-oxotetracyclo[4.3.2.22,5.01,6]trideca-3,8,10,12-tetraene-3-carboxylate化学式
CAS
131236-20-9
化学式
C15H12O3
mdl
——
分子量
240.258
InChiKey
ZGTFPVYEPUIKJX-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):
    1.58
  • 重原子数:
    18.0
  • 可旋转键数:
    1.0
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    43.37
  • 氢给体数:
    0.0
  • 氢受体数:
    3.0

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    methyl 7-oxotetracyclo[4.3.2.22,5.01,6]trideca-3,8,10,12-tetraene-3-carboxylate 在 potassium diazodicarboxylate 、 溶剂黄146 作用下, 以 乙腈 为溶剂, 以8%的产率得到methyl 7-oxotetracyclo[4.3.2.22,5.01,6]trideca-3,8-diene-3-carboxylate
    参考文献:
    名称:
    .pi.-Facial selectivity in Diels-Alder reactions of [4.3.2]propella-2,4,8,10-tetraen-7-one and its derivatives. Synthesis of 2,5-etheno[4.3.2]propella-3,8,10-trien-7-ones
    摘要:
    The Diels-Alder additions of dimethyl acetylenedicarboxylate, methyl propiolate, and maleic anhydride to [4.3.2]propella-2,4,8,10-tetraen-7-one (1), and its 8,9- and 10,11-dihydro derivatives, 2 and 3, and [4.3.2]propella-2,4,7,10-tetraene (4) occur steroselectively at the face of cyclohexadiene ring syn to five-membered ring. The-pi-facial selectivity of the additions is rationalized in terms of difference in dihedral angles between the cyclohexadiene and two flanking rings. Treatment of the adduct of maleic anhydride to 1 with Ni(PPh3)2(CO)2 gives 2,5-etheno[4.3.2]propella-3,8,10-trien-7-one (5a). The electronic absorption spectrum of 5a exhibits characteristic longer wave absorptions compared with the corresponding partly saturated derivatives, suggesting the existence of longicyclic interaction among its four-pi-bonds. Irradiation of 5a results in transannular [2 + 2] cycloaddition rather than cleavage into antiaromatic bicyclo[3.2.0]heptatrienone and benzene.
    DOI:
    10.1021/jo00003a020
  • 作为产物:
    描述:
    参考文献:
    名称:
    TSUJI, TAKASHI;OHKITA, MASAKAZU;NISHIDA, SHINYA, J. ORG. CHEM., 56,(1991) N, C. 997-1003
    摘要:
    DOI:
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