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1-Cyclopropylocta-1,7-diyn-3-ol | 1427329-96-1

中文名称
——
中文别名
——
英文名称
1-Cyclopropylocta-1,7-diyn-3-ol
英文别名
1-cyclopropylocta-1,7-diyn-3-ol
1-Cyclopropylocta-1,7-diyn-3-ol化学式
CAS
1427329-96-1
化学式
C11H14O
mdl
——
分子量
162.232
InChiKey
JIWDXEPIZDMVJY-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):
    2
  • 重原子数:
    12
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.64
  • 拓扑面积:
    20.2
  • 氢给体数:
    1
  • 氢受体数:
    1

反应信息

  • 作为反应物:
    描述:
    1-Cyclopropylocta-1,7-diyn-3-ol三苯基膦偶氮二甲酸二乙酯 、 o-nitrobenzylsulfonylhydrazine 作用下, 以 四氢呋喃 为溶剂, 生成 1-(octa-1,2-dien-7-yn-1-yl)cyclopropane
    参考文献:
    名称:
    Application of In Situ-Generated Rh-Bound Trimethylenemethane Variants to the Synthesis of 3,4-Fused Pyrroles
    摘要:
    Rh-bound trimethylenemethane variants generated from the interaction of a Rh-carbenoid with an allene have been applied to the synthesis of substituted 3,4-fused pyrroles. The pyrrole products are useful starting points for the syntheses of various dipyrromethene ligands. Furthermore, the methodology has been applied to a synthesis of the natural product cycloprodigiosin, which demonstrates antitumor and immunosuppressor activity.
    DOI:
    10.1021/ja401380d
  • 作为产物:
    参考文献:
    名称:
    Application of In Situ-Generated Rh-Bound Trimethylenemethane Variants to the Synthesis of 3,4-Fused Pyrroles
    摘要:
    Rh-bound trimethylenemethane variants generated from the interaction of a Rh-carbenoid with an allene have been applied to the synthesis of substituted 3,4-fused pyrroles. The pyrrole products are useful starting points for the syntheses of various dipyrromethene ligands. Furthermore, the methodology has been applied to a synthesis of the natural product cycloprodigiosin, which demonstrates antitumor and immunosuppressor activity.
    DOI:
    10.1021/ja401380d
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文献信息

  • Application of In Situ-Generated Rh-Bound Trimethylenemethane Variants to the Synthesis of 3,4-Fused Pyrroles
    作者:Erica E. Schultz、Richmond Sarpong
    DOI:10.1021/ja401380d
    日期:2013.3.27
    Rh-bound trimethylenemethane variants generated from the interaction of a Rh-carbenoid with an allene have been applied to the synthesis of substituted 3,4-fused pyrroles. The pyrrole products are useful starting points for the syntheses of various dipyrromethene ligands. Furthermore, the methodology has been applied to a synthesis of the natural product cycloprodigiosin, which demonstrates antitumor and immunosuppressor activity.
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