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(E)-6-methyl-1,8-diphenyloct-7-en-1-one | 1353557-75-1

中文名称
——
中文别名
——
英文名称
(E)-6-methyl-1,8-diphenyloct-7-en-1-one
英文别名
——
(E)-6-methyl-1,8-diphenyloct-7-en-1-one化学式
CAS
1353557-75-1
化学式
C21H24O
mdl
——
分子量
292.421
InChiKey
IXVPAWJXSPISCP-WUKNDPDISA-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):
    5.9
  • 重原子数:
    22
  • 可旋转键数:
    8
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    17.1
  • 氢给体数:
    0
  • 氢受体数:
    1

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    6-bromo-1-phenylheptan-1-one反式-2-苯乙烯硼酸频哪酸酯叔丁基锂十一烷FeCl2(TMS-SciOPP) 、 magnesium bromide 作用下, 以 四氢呋喃正戊烷 为溶剂, 反应 25.0h, 以83%的产率得到(E)-6-methyl-1,8-diphenyloct-7-en-1-one
    参考文献:
    名称:
    Stereospecific Cross-Coupling between Alkenylboronates and Alkyl Halides Catalyzed by Iron–Bisphosphine Complexes
    摘要:
    A stereospecific and high-yielding cross-coupling reaction between alkenylboron reagents and alkyl halides is described. The reaction has been achieved by using well-defined iron bisphosphine complexes such as 1b FeCl2(3,5-t-Bu-2-SciOPP), which was recently developed by the authors' group. Various nonactivated alkyl bromides and chlorides possessing a base/nucleophile-sensitive functional group can participate in the cross-coupling, demonstrating its utility for stereoselective synthesis of functional molecules bearing a carbon carbon double bond.
    DOI:
    10.1021/jo202151f
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文献信息

  • Stereospecific Cross-Coupling between Alkenylboronates and Alkyl Halides Catalyzed by Iron–Bisphosphine Complexes
    作者:Toru Hashimoto、Takuji Hatakeyama、Masaharu Nakamura
    DOI:10.1021/jo202151f
    日期:2012.1.20
    A stereospecific and high-yielding cross-coupling reaction between alkenylboron reagents and alkyl halides is described. The reaction has been achieved by using well-defined iron bisphosphine complexes such as 1b FeCl2(3,5-t-Bu-2-SciOPP), which was recently developed by the authors' group. Various nonactivated alkyl bromides and chlorides possessing a base/nucleophile-sensitive functional group can participate in the cross-coupling, demonstrating its utility for stereoselective synthesis of functional molecules bearing a carbon carbon double bond.
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