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2,2-cyclohexyl-5-[(E)-2-(4-methoxyphenyl)-4-oxo-6-phenylhex-5-enyl]-1,3-dioxane-4,6-dione | 1089672-19-4

中文名称
——
中文别名
——
英文名称
2,2-cyclohexyl-5-[(E)-2-(4-methoxyphenyl)-4-oxo-6-phenylhex-5-enyl]-1,3-dioxane-4,6-dione
英文别名
3-[(E)-2-(4-methoxyphenyl)-4-oxo-6-phenylhex-5-enyl]-1,5-dioxaspiro[5.5]undecane-2,4-dione
2,2-cyclohexyl-5-[(E)-2-(4-methoxyphenyl)-4-oxo-6-phenylhex-5-enyl]-1,3-dioxane-4,6-dione化学式
CAS
1089672-19-4
化学式
C28H30O6
mdl
——
分子量
462.543
InChiKey
QFZWVRSKDWJITE-JLHYYAGUSA-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):
    5.5
  • 重原子数:
    34
  • 可旋转键数:
    8
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.39
  • 拓扑面积:
    78.9
  • 氢给体数:
    0
  • 氢受体数:
    6

反应信息

  • 作为产物:
    描述:
    {(1E)-3-[(trimethylsilyl)oxy]buta-1,3-dien-1-yl}benzenescandium tris(trifluoromethanesulfonate) 作用下, 以 二氯甲烷 为溶剂, 以54%的产率得到2,2-cyclohexyl-5-[(E)-2-(4-methoxyphenyl)-4-oxo-6-phenylhex-5-enyl]-1,3-dioxane-4,6-dione
    参考文献:
    名称:
    Sc(OTf)3-catalyzed smooth tandem [3+2] cycloaddition/ring opening of donor–acceptor cyclopropane 1,1-diesters with enol silyl ethers
    摘要:
    Catalyzed by Lewis acids, donor-acceptor cyclopropane 1,1-diesters reacted with enol silyl ethers to afford 1,6-dicarbonyl compounds in moderate to excellent yields. This supplied a mild carbon-carbon bond-forming method from the ring opening of cyclopropanes. A smooth tandem [3+2] cycloaddition/ring opening process has been clearly proved by an independent experiment. (C) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2008.09.028
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文献信息

  • Sc(OTf)3-catalyzed smooth tandem [3+2] cycloaddition/ring opening of donor–acceptor cyclopropane 1,1-diesters with enol silyl ethers
    作者:Jie Fang、Jun Ren、Zhongwen Wang
    DOI:10.1016/j.tetlet.2008.09.028
    日期:2008.11
    Catalyzed by Lewis acids, donor-acceptor cyclopropane 1,1-diesters reacted with enol silyl ethers to afford 1,6-dicarbonyl compounds in moderate to excellent yields. This supplied a mild carbon-carbon bond-forming method from the ring opening of cyclopropanes. A smooth tandem [3+2] cycloaddition/ring opening process has been clearly proved by an independent experiment. (C) 2008 Elsevier Ltd. All rights reserved.
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