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1-(3-(6-phenylindolizin-8-yl)phenyl)ethanone | 1418760-44-7

中文名称
——
中文别名
——
英文名称
1-(3-(6-phenylindolizin-8-yl)phenyl)ethanone
英文别名
1-[3-(6-Phenylindolizin-8-yl)phenyl]ethanone;1-[3-(6-phenylindolizin-8-yl)phenyl]ethanone
1-(3-(6-phenylindolizin-8-yl)phenyl)ethanone化学式
CAS
1418760-44-7
化学式
C22H17NO
mdl
——
分子量
311.383
InChiKey
AOSYYVGAEADYKX-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):
    5.4
  • 重原子数:
    24
  • 可旋转键数:
    3
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.05
  • 拓扑面积:
    21.5
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

  • 作为产物:
    描述:
    2-乙酰基吡咯potassium phosphate四(三苯基膦)钯 、 sodium hydride 、 potassium carbonate 作用下, 以 四氢呋喃乙腈 为溶剂, 反应 28.0h, 生成 1-(3-(6-phenylindolizin-8-yl)phenyl)ethanone
    参考文献:
    名称:
    Cycloaromatization Approach to Polysubstituted Indolizines from 2-Acetylpyrroles: Decoration of the Pyridine Unit
    摘要:
    A new synthetic route to indolizines with various substituents on the pyridine moiety was developed by utilizing a facile cycloaromatization of 2-acetylpyrrole derivatives. Without isolation, the resulting intermediates were allowed to react with various electrophiles to afford a range of indolizines. In particular, Suzuki-Miyaura cross-coupling of O-triflates with (hetero)arylboronic acids permitted introduction of diverse substituents at the C8 position of an indolizine skeleton.
    DOI:
    10.1021/jo302590a
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文献信息

  • Cycloaromatization Approach to Polysubstituted Indolizines from 2-Acetylpyrroles: Decoration of the Pyridine Unit
    作者:Jin Ho Lee、Ikyon Kim
    DOI:10.1021/jo302590a
    日期:2013.2.1
    A new synthetic route to indolizines with various substituents on the pyridine moiety was developed by utilizing a facile cycloaromatization of 2-acetylpyrrole derivatives. Without isolation, the resulting intermediates were allowed to react with various electrophiles to afford a range of indolizines. In particular, Suzuki-Miyaura cross-coupling of O-triflates with (hetero)arylboronic acids permitted introduction of diverse substituents at the C8 position of an indolizine skeleton.
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