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Methyl 2-<2-(1-bromo-2-oxopropyl)cyclopentyl>ethanoate | 136202-55-6

中文名称
——
中文别名
——
英文名称
Methyl 2-<2-(1-bromo-2-oxopropyl)cyclopentyl>ethanoate
英文别名
——
Methyl 2-<2-(1-bromo-2-oxopropyl)cyclopentyl>ethanoate化学式
CAS
136202-55-6;136314-80-2
化学式
C11H17BrO3
mdl
——
分子量
277.158
InChiKey
QNGRCMFJCARWJR-VFXVZZSQSA-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):
    2.32
  • 重原子数:
    15.0
  • 可旋转键数:
    4.0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.82
  • 拓扑面积:
    43.37
  • 氢给体数:
    0.0
  • 氢受体数:
    3.0

反应信息

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文献信息

  • Cyclization Reactions of Allylic O-Stannyl Ketyls
    作者:Eric J. Enholm、Kevin S. Kinter
    DOI:10.1021/jo00120a031
    日期:1995.7
    This is a summary of an investigation of the tributyltin hydride-induced cyclization reactions of unsaturated ketones with electronically deficient olefins. This reaction was initiated by an O-stannyl ketyl formed by the addition of a tributyltin radical to a carbonyl, which has both anionic and radical character. The intramolecular coupling produced functionalized cyclopentanes, bearing two synthetically useful carbon appendages. An activating or electron-withdrawing function on the alkene was essential to the cyclization. A dilution study revealed that excellent anti stereoselectivities (>50:1) could be achieved, and this was attributed to a reversible cyclization. Another goal of this study was to separate the radical reactivity from the anionic reactivity of the O-stannyl ketyl by the participation of labile functional groups and external electrophiles. The presence of minor products and enolate-trapping studies demonstrated that the anionic character of the ketyl could be utilized in the form of a tin enolate. This work represents the first free radical- and reagent-based approach to the study of the intramolecular hydrodimerization of activated alkenes.
  • Enholm, Eric J.; Kinter, Kevin S., Journal of the American Chemical Society, 1991, vol. 113, # 20, p. 7784 - 7785
    作者:Enholm, Eric J.、Kinter, Kevin S.
    DOI:——
    日期:——
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