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dimethyl 2,3,6,7,8,8a-hexahydro-7-oxa-1H-3a,6-epoxyazulene-4,5-dicarboxylate | 126252-67-3

中文名称
——
中文别名
——
英文名称
dimethyl 2,3,6,7,8,8a-hexahydro-7-oxa-1H-3a,6-epoxyazulene-4,5-dicarboxylate
英文别名
4,5-dicarbomethoxy-2,3,6,7,8,8a-hexahydro-7-oxa-1H-3a,b-epoxyazulene;Dimethyl 7-oxo-11-oxatricyclo[6.2.1.01,5]undec-9-ene-9,10-dicarboxylate
dimethyl 2,3,6,7,8,8a-hexahydro-7-oxa-1H-3a,6-epoxyazulene-4,5-dicarboxylate化学式
CAS
126252-67-3
化学式
C14H16O6
mdl
——
分子量
280.277
InChiKey
FZFOABJUWXMCBN-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):
    0.2
  • 重原子数:
    20
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.64
  • 拓扑面积:
    78.9
  • 氢给体数:
    0
  • 氢受体数:
    6

反应信息

  • 作为反应物:
    描述:
    dimethyl 2,3,6,7,8,8a-hexahydro-7-oxa-1H-3a,6-epoxyazulene-4,5-dicarboxylate乙腈 为溶剂, 反应 2.0h, 以96%的产率得到dimethyl 3a,4,5a,6,7,8-hexahydro-4-oxa-5H-pentaleno<6a,1-b>furan-3,3a-dicarboxylate
    参考文献:
    名称:
    Studies dealing with the excited-state behavior of substituted 8-oxabicyclo[3.2.1]oct-6-en-2-ones
    摘要:
    A series of 8-oxabicyclo [3.2.1]oct-6-en-2-ones was prepared by the rhodium(II)-catalyzed cyclization-cycloaddition reaction of alpha-diazopentanedione with various alkynes. The photochemical behavior of these oxabicyclic enones was investigated. Both direct and sensitized photolysis cleanly results in a 1,3-acyl shift. A slower, secondary photoprocess involving intramolecular hydrogen atom transfer and intramolecular cycloaddition of the resulting ketene was also uncovered. The photobehavior of the closely related 9-oxabenzocycloheptene system was also examined. The initially formed 1,3-sigmatropic rearranged product was found to undergo a novel 1,4-methoxyl migration on extended photolysis. The photochemistry of the homologous 7-oxabicyclo[2.2.1]hepten-2-one was studied. The results obtained can be interpreted in terms of an initial Norrish type I cleavage. The resulting diradical either couples to give the 1,3-acyl shift product or undergoes bond fragmentation, giving products derived from a stepwise retro-Diels-Alder reaction.
    DOI:
    10.1021/jo00003a032
  • 作为产物:
    描述:
    在 dirhodium tetraacetate 、 丁炔二酸二甲酯 作用下, 以 乙醚 为溶剂, 反应 12.0h, 生成 dimethyl 2,3,6,7,8,8a-hexahydro-7-oxa-1H-3a,6-epoxyazulene-4,5-dicarboxylate
    参考文献:
    名称:
    铑卡宾的串联环化-环加成反应。过程的范围和机械细节
    摘要:
    Reactions de diazo-1 pentanediones-2,5 avec des carboxyates de rhodium(II) qui Fourtnissent desylures cycliques reactifs
    DOI:
    10.1021/ja00164a034
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文献信息

  • Photochemical rearrangement of 8-oxabicyclo[3.2.1]oct-6-en-2-ones
    作者:Albert Padwa、Glen E. Fryxell、Lin Zhi、Susan F. Hornbuckle
    DOI:10.1016/s0040-4039(00)88467-1
    日期:1988.1
  • PADWA, ALBERT;FRYXELL, GLEN E.;ZHI, LIN, J. AMER. CHEM. SOC., 112,(1990) N, C. 3100-3109
    作者:PADWA, ALBERT、FRYXELL, GLEN E.、ZHI, LIN
    DOI:——
    日期:——
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