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methyl 6-(3-triethylsilyloxy-2-((E)-4-triethylsilyloxy-4-methyloct-1-enyl)-5-oxocyclopentyl)hexanoate | 1184962-04-6

中文名称
——
中文别名
——
英文名称
methyl 6-(3-triethylsilyloxy-2-((E)-4-triethylsilyloxy-4-methyloct-1-enyl)-5-oxocyclopentyl)hexanoate
英文别名
methyl 6-[2-[(E)-4-methyl-4-triethylsilyloxyoct-1-enyl]-5-oxo-3-triethylsilyloxycyclopentyl]hexanoate
methyl 6-(3-triethylsilyloxy-2-((E)-4-triethylsilyloxy-4-methyloct-1-enyl)-5-oxocyclopentyl)hexanoate化学式
CAS
1184962-04-6
化学式
C33H64O5Si2
mdl
——
分子量
597.039
InChiKey
ZVOJCNAKXMIOPJ-XTQSDGFTSA-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):
    9.62
  • 重原子数:
    40
  • 可旋转键数:
    23
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.88
  • 拓扑面积:
    61.8
  • 氢给体数:
    0
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    描述:
    methyl 6-(3-triethylsilyloxy-2-((E)-4-triethylsilyloxy-4-methyloct-1-enyl)-5-oxocyclopentyl)hexanoate2,3-二氯-5,6-二氰基-1,4-苯醌 作用下, 以 乙腈 为溶剂, 反应 4.0h, 以60%的产率得到methyl 6-(3-hydroxy-2-((E)-4-hydroxy-4-methyloct-1-enyl)-5-oxocyclopentyl)hexanoate
    参考文献:
    名称:
    Synthesis of 2-Normisoprostol, Methyl 6-(3-Hydroxy-2-((E)-4-hydroxy-4-methyloct-1-enyl)-5-oxocyclopentyl)hexanoate
    摘要:
    Synthesis of 2-normisoprostol, methyl 6-(3-hydroxy-2-((E)-4-hydroxy-4-methyloct-1-enyl)-5-oxocyclopentyl)hexanoate (3), employing two-component coupling strategy based on 1,4-addition followed by DDQ-mediated triethyl silyl deprotection is reported. Desired key intermediates, methyl 6-(3-triethyl silyloxy-5-oxocyclopent-1-enyl)hexanoate (4) and (E)-1-(tributylstannyl)-4-methyloct-1-en-4-yloxy)triethylsilane (5), were prepared from commercially available cycloheptanone and propargyl bromide, and the intermediates were coupled to obtain 3 in a convergent approach.
    DOI:
    10.1080/00397910802664228
  • 作为产物:
    描述:
    methyl 6-(3-triethylsilyloxy-5-oxocyclopent-1-enyl)hexanoate4-Methyl-1-octin-4(RS)-ol-triethylsilylether偶氮二异丁腈三正丁基氢锡甲基锂copper(l) cyanide 作用下, 以 四氢呋喃 为溶剂, 反应 3.0h, 以3.8 g的产率得到methyl 6-(3-triethylsilyloxy-2-((E)-4-triethylsilyloxy-4-methyloct-1-enyl)-5-oxocyclopentyl)hexanoate
    参考文献:
    名称:
    Synthesis of 2-Normisoprostol, Methyl 6-(3-Hydroxy-2-((E)-4-hydroxy-4-methyloct-1-enyl)-5-oxocyclopentyl)hexanoate
    摘要:
    Synthesis of 2-normisoprostol, methyl 6-(3-hydroxy-2-((E)-4-hydroxy-4-methyloct-1-enyl)-5-oxocyclopentyl)hexanoate (3), employing two-component coupling strategy based on 1,4-addition followed by DDQ-mediated triethyl silyl deprotection is reported. Desired key intermediates, methyl 6-(3-triethyl silyloxy-5-oxocyclopent-1-enyl)hexanoate (4) and (E)-1-(tributylstannyl)-4-methyloct-1-en-4-yloxy)triethylsilane (5), were prepared from commercially available cycloheptanone and propargyl bromide, and the intermediates were coupled to obtain 3 in a convergent approach.
    DOI:
    10.1080/00397910802664228
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文献信息

  • Synthesis of 2-Normisoprostol, Methyl 6-(3-Hydroxy-2-((<i>E</i>)-4-hydroxy-4-methyloct-1-enyl)-5-oxocyclopentyl)hexanoate
    作者:M. Harikrishna、H. Rama Mohan、P. K. Dubey、Gottumukkala V. Subbaraju
    DOI:10.1080/00397910802664228
    日期:2009.7.7
    Synthesis of 2-normisoprostol, methyl 6-(3-hydroxy-2-((E)-4-hydroxy-4-methyloct-1-enyl)-5-oxocyclopentyl)hexanoate (3), employing two-component coupling strategy based on 1,4-addition followed by DDQ-mediated triethyl silyl deprotection is reported. Desired key intermediates, methyl 6-(3-triethyl silyloxy-5-oxocyclopent-1-enyl)hexanoate (4) and (E)-1-(tributylstannyl)-4-methyloct-1-en-4-yloxy)triethylsilane (5), were prepared from commercially available cycloheptanone and propargyl bromide, and the intermediates were coupled to obtain 3 in a convergent approach.
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