摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

anti-CH3O2CC(Sn(C4H9)3)C(CO2CH3)C4H3O | 1011497-79-2

中文名称
——
中文别名
——
英文名称
anti-CH3O2CC(Sn(C4H9)3)C(CO2CH3)C4H3O
英文别名
——
anti-CH3O2CC(Sn(C4H9)3)C(CO2CH3)C4H3O化学式
CAS
1011497-79-2
化学式
C22H36O5Sn
mdl
——
分子量
499.235
InChiKey
IXWUZDOFAXQTGQ-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):
    5.77
  • 重原子数:
    28
  • 可旋转键数:
    15
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.64
  • 拓扑面积:
    65.7
  • 氢给体数:
    0
  • 氢受体数:
    5

反应信息

  • 作为产物:
    描述:
    2-(三丁基锡烷基)呋喃丁炔二酸二甲酯 在 tris(dibenzylideneacetone)dipalladium (0) 作用下, 以 二氯甲烷 为溶剂, 生成 anti-CH3O2CC(Sn(C4H9)3)C(CO2CH3)C4H3Oanti-CH3O2CC(Sn(C4H9)3)C(CO2CH3)C4H3O
    参考文献:
    名称:
    Alkynes as Stille Reaction Pseudohalides:  Gold- and Palladium-Cocatalyzed Synthesis of Tri- and Tetra-Substituted Olefins
    摘要:
    A Stille-type reaction that employs alkynes as pseudohalides provides access to the catalytic chemistry of palladium-carbon sigma-bonds starting from pi-systems. The synthesis of a variety of tri- and tetra-substituted olefins by addition of sp(2)- and sp-hybridized stannanes across mono- and diester alkynes was accomplished with complete regioselectivity and high stereoselectivity. The reaction is proposed to proceed via a bimetallic mechanism where the Lewis acidic Au(I) activates the alkyne toward oxidative addition across Pd(0).
    DOI:
    10.1021/ja710648b
点击查看最新优质反应信息

文献信息

  • Alkynes as Stille Reaction Pseudohalides:  Gold- and Palladium-Cocatalyzed Synthesis of Tri- and Tetra-Substituted Olefins
    作者:Yili Shi、Sonja M. Peterson、Walter W. Haberaecker、Suzanne A. Blum
    DOI:10.1021/ja710648b
    日期:2008.2.1
    A Stille-type reaction that employs alkynes as pseudohalides provides access to the catalytic chemistry of palladium-carbon sigma-bonds starting from pi-systems. The synthesis of a variety of tri- and tetra-substituted olefins by addition of sp(2)- and sp-hybridized stannanes across mono- and diester alkynes was accomplished with complete regioselectivity and high stereoselectivity. The reaction is proposed to proceed via a bimetallic mechanism where the Lewis acidic Au(I) activates the alkyne toward oxidative addition across Pd(0).
查看更多