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diethyl 2--3-methylbutanedioate | 141527-60-8

中文名称
——
中文别名
——
英文名称
diethyl 2--3-methylbutanedioate
英文别名
diethyl 2-(tris(trimethylsilyl)silyl)-3-methylbutanedioate;diethyl (2R,3S)-2-methyl-3-tris(trimethylsilyl)silylbutanedioate
diethyl 2-<tris(trimethylsilyl)silyl>-3-methylbutanedioate化学式
CAS
141527-60-8
化学式
C18H42O4Si4
mdl
——
分子量
434.871
InChiKey
KLJQFCACPBPQIS-HOTGVXAUSA-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):
    4.82
  • 重原子数:
    26
  • 可旋转键数:
    11
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.89
  • 拓扑面积:
    52.6
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    三(三甲基硅基)硅烷二乙基(2E)-2-甲基-2-丁烯二酸酯偶氮二异丁腈 作用下, 以 甲苯 为溶剂, 反应 1.0h, 生成 diethyl 2--3-methylbutanedioate 、 diethyl 2--3-methylbutanedioate
    参考文献:
    名称:
    Tris(trimethylsilyl)silane: an efficient hydrosilylating agent of alkenes and alkynes
    摘要:
    Tris(trimethylsilyl)silane adds across the double bond of a variety of mono-, di-, and trisubstituted olefins under free-radical conditions in good yields. The reaction, which proceeds via a free-radical chain mechanism, is highly regioselective (anti-Markovnikov). Addition to prochiral olefins bearing an ester group is highly stereoselective. The factors that control the stereochemistry have been discussed terms of preferred conformations of the intermediate carbon-centered radicals and are thought to be of steric origin.
    DOI:
    10.1021/jo00040a048
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文献信息

  • Tris(trimethylsilyl)silane: an efficient hydrosilylating agent of alkenes and alkynes
    作者:B. Kopping、C. Chatgilialoglu、M. Zehnder、B. Giese
    DOI:10.1021/jo00040a048
    日期:1992.7
    Tris(trimethylsilyl)silane adds across the double bond of a variety of mono-, di-, and trisubstituted olefins under free-radical conditions in good yields. The reaction, which proceeds via a free-radical chain mechanism, is highly regioselective (anti-Markovnikov). Addition to prochiral olefins bearing an ester group is highly stereoselective. The factors that control the stereochemistry have been discussed terms of preferred conformations of the intermediate carbon-centered radicals and are thought to be of steric origin.
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