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Te-Butyl (phenylthio)ethanetelluroate | 160463-35-4

中文名称
——
中文别名
——
英文名称
Te-Butyl (phenylthio)ethanetelluroate
英文别名
Te-butyl 2-phenylsulfanylethanetelluroate
Te-Butyl (phenylthio)ethanetelluroate化学式
CAS
160463-35-4
化学式
C12H16OSTe
mdl
——
分子量
335.924
InChiKey
SJVVDLDQUZTTJD-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):
    3.23
  • 重原子数:
    15
  • 可旋转键数:
    7
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.42
  • 拓扑面积:
    42.4
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

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文献信息

  • Conversion of Tellurol Esters to Enol Silyl Ethers of Acylsilanes
    作者:Toru Inoue、Nobuaki Kambe、Ilhyong Ryu、Noboru Sonoda
    DOI:10.1021/jo00105a044
    日期:1994.12
    Tellurol esters having an anion stabilizing group at the position alpha to the carbonyl, such as aryl-, (phenylthio)-, and (benzyloxy)ethenetelluroates, gave enol silyl ethers of the corresponding acylsilanes in good to excellent yields upon treatment with 2 equiv of (n)BuLi in the presence of chlorosilanes. This reaction was stereoselective, and Z-isomers were obtained as sole or major products from a variety of chlorosilanes, such as trimethyl-, triethyl-, dimethylphenyl-, and tert-butyldimethylsilyl chlorides. Control experiments revealed that the reaction comprises the following consecutive processes: (i) alpha-proton abstraction, (ii) chlorosilane-trapping, (iii) lithium-tellurium exchange, (iv) 1,2-silyl migration, and (v) chlorosilane-trapping. Intramolecular rearrangement of (alpha-siloxyvinyl)lithiums to lithium enolates (step iv) was very fast even at -105 degrees C, and the former could not be trapped intermolecularly either with acetic acid or with coexisting trimethylsilyl chloride.
  • Inoue Toru, Kambe Nobuaki, Ryu Ilhyong, Sonoda Noboru, J. Org. Chem, 59 (1994) N 26, S 8209-8214
    作者:Inoue Toru, Kambe Nobuaki, Ryu Ilhyong, Sonoda Noboru
    DOI:——
    日期:——
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