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ethyl (Z)-3-(2-hexyl-4-methyl-5-tributylstannylphenyl)prop-2-enoate | 820964-98-5

中文名称
——
中文别名
——
英文名称
ethyl (Z)-3-(2-hexyl-4-methyl-5-tributylstannylphenyl)prop-2-enoate
英文别名
——
ethyl (Z)-3-(2-hexyl-4-methyl-5-tributylstannylphenyl)prop-2-enoate化学式
CAS
820964-98-5
化学式
C30H52O2Sn
mdl
——
分子量
563.452
InChiKey
DFQWTIZOFWFDCN-XXXTXXBHSA-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:
    562.4±60.0 °C(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    8.75
  • 重原子数:
    33.0
  • 可旋转键数:
    18.0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.7
  • 拓扑面积:
    26.3
  • 氢给体数:
    0.0
  • 氢受体数:
    2.0

SDS

SDS:06bc8184f92495ce78f282bec2e0c864
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反应信息

  • 作为产物:
    描述:
    三丁基氧化锡2-甲基-1-丁烯-3-炔ethyl (Z)-undec-2-en-4-ynoate马来酸酐N-[2-(二苯基膦)苯亚甲基]环己胺 作用下, 以 四氢呋喃 为溶剂, 以89%的产率得到ethyl (Z)-3-(2-hexyl-4-methyl-5-tributylstannylphenyl)prop-2-enoate
    参考文献:
    名称:
    Stannylative Cycloaddition of Enynes Catalyzed by Palladium−Iminophosphine
    摘要:
    Palladium-iminophosphine complex catalyzes stannylative cycloaddition of conjugated enynes using hexabutyldistannoxane as a stannylating agent to afford highly substituted 3-alkenylphenylstannanes regioselectively. Stannylative cross-cycloaddition reactions between different enynes or between enynes and diynes are also achieved. The reaction is successfully applied to a concise synthesis of alcyopterosin N, which has been isolated recently from sub-Antarctic soft coral, Alcyonium paessleri.
    DOI:
    10.1021/ja044429s
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文献信息

  • Stannylative Cycloaddition of Enynes Catalyzed by Palladium−Iminophosphine
    作者:Yoshiaki Nakao、Yasuhiro Hirata、Shinjiro Ishihara、Shinichi Oda、Tomoya Yukawa、Eiji Shirakawa、Tamejiro Hiyama
    DOI:10.1021/ja044429s
    日期:2004.12.1
    Palladium-iminophosphine complex catalyzes stannylative cycloaddition of conjugated enynes using hexabutyldistannoxane as a stannylating agent to afford highly substituted 3-alkenylphenylstannanes regioselectively. Stannylative cross-cycloaddition reactions between different enynes or between enynes and diynes are also achieved. The reaction is successfully applied to a concise synthesis of alcyopterosin N, which has been isolated recently from sub-Antarctic soft coral, Alcyonium paessleri.
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