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(Z)-3-tributylstannyl-1-ethoxy-4-trimethylsilylbut-1-ene | 161980-09-2

中文名称
——
中文别名
——
英文名称
(Z)-3-tributylstannyl-1-ethoxy-4-trimethylsilylbut-1-ene
英文别名
[(Z)-4-ethoxy-2-tributylstannylbut-3-enyl]-trimethylsilane
(Z)-3-tributylstannyl-1-ethoxy-4-trimethylsilylbut-1-ene化学式
CAS
161980-09-2
化学式
C21H46OSiSn
mdl
——
分子量
461.391
InChiKey
ZEJKFWOCRICLGL-SKAPHXEVSA-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

物化性质

  • 沸点:
    440.6±55.0 °C(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    8.09
  • 重原子数:
    24
  • 可旋转键数:
    15
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.9
  • 拓扑面积:
    9.2
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

  • 作为反应物:
    描述:
    3-甲基-2-丁烯醛(Z)-3-tributylstannyl-1-ethoxy-4-trimethylsilylbut-1-ene三氟化硼乙醚 作用下, 以 二氯甲烷 为溶剂, 反应 1.0h, 生成 (E)-(4S,5R)-5-Ethoxy-2-methyl-8-trimethylsilanyl-octa-2,6-dien-4-ol 、 (E)-(4R,5R)-5-Ethoxy-2-methyl-8-trimethylsilanyl-octa-2,6-dien-4-ol
    参考文献:
    名称:
    Addition of α-Substituted (γ-Alkoxyallyl)tins on Aldehydes:  The Dramatic Influence of the Size of the α-Substituent on the Diastereoselection
    摘要:
    DOI:
    10.1021/jo9708203
  • 作为产物:
    描述:
    参考文献:
    名称:
    Watrelot Sandrine, Parrain Jean-Luc, Quintard Jean-Paul, J. Org. Chem, 59 (1994) N 26, S 7959- 7961
    摘要:
    DOI:
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文献信息

  • Preparation of α-substituted γ-alkoxyallylstannanes from β-tributylstannyl acrolein acetals: scope of the method and primary rationalization of the obtained results
    作者:Florian Fliegel、Isabelle Beaudet、Sandrine Watrelot-Bourdeau、Nicolas Cornet、Jean-Paul Quintard
    DOI:10.1016/j.jorganchem.2004.10.022
    日期:2005.1
    alpha-Substituted gamma-alkoxyallylstannanes were obtained from beta-tributylstannyl acrolein acetals when reacted with lower order magnesium cyanocuprates in the presence of boron trifluoride at low temperature. In the case of n-alkylcyanocuprates an anti S(N)2' substitution on a cisoid conformation appears to be the main reaction pathway. However, subtle competitions with other mechanisms may occur depending on the experimental conditions, on the reagents or on the substrates. These drawbacks constitute limitations for the use of the method especially when enantioenriched alpha-substituted gamma-alkoxyallylstannanes are desired. (C) 2004 Elsevier B.V. All rights reserved.
  • Watrelot Sandrine, Parrain Jean-Luc, Quintard Jean-Paul, J. Org. Chem, 59 (1994) N 26, S 7959- 7961
    作者:Watrelot Sandrine, Parrain Jean-Luc, Quintard Jean-Paul
    DOI:——
    日期:——
  • Addition of α-Substituted (γ-Alkoxyallyl)tins on Aldehydes:  The Dramatic Influence of the Size of the α-Substituent on the Diastereoselection
    作者:Sandrine Watrelot-Bourdeau、Jean-Luc Parrain、Jean-Paul Quintard
    DOI:10.1021/jo9708203
    日期:1997.11.1
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