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5-(4-methoxyphenyl)-1-methyl-3,4-diphenyl-6,7-dihydro-4H-furo[3,4-c]pyridine | 1009319-39-4

中文名称
——
中文别名
——
英文名称
5-(4-methoxyphenyl)-1-methyl-3,4-diphenyl-6,7-dihydro-4H-furo[3,4-c]pyridine
英文别名
——
5-(4-methoxyphenyl)-1-methyl-3,4-diphenyl-6,7-dihydro-4H-furo[3,4-c]pyridine化学式
CAS
1009319-39-4
化学式
C27H25NO2
mdl
——
分子量
395.501
InChiKey
NWJXPXPNEIBVHC-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):
    6.4
  • 重原子数:
    30
  • 可旋转键数:
    4
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.19
  • 拓扑面积:
    25.6
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    1-(1-(phenylethynyl)cyclopropyl)ethanone4-methoxy-N-[(E)-phenylmethylidene]aniline 在 IPrAuNTf2 作用下, 以 1,2-二氯乙烷 为溶剂, 反应 22.0h, 以68%的产率得到5-(4-methoxyphenyl)-1-methyl-3,4-diphenyl-6,7-dihydro-4H-furo[3,4-c]pyridine
    参考文献:
    名称:
    Au-Containing All-Carbon 1,4-Dipoles:  Generation and [4 + 2] Annulation in the Formation of Carbo-/Heterocycles
    摘要:
    A novel concept of Au-containing all-carbon 1,n-dipoles is advanced. From 1-(1-alkynyl) cyclopropyl ketones, Au-containing all-carbon 1,4-dipoles are presumably generated in situ and can efficiently participate in [4 + 2] annulation with dipolarophiles including indoles, various carbonyl compounds, imines, and silyl enol ethers. Polycyclic, fully substituted furans are readily synthesized under mild reaction conditions.
    DOI:
    10.1021/ja077948e
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文献信息

  • Au-Containing All-Carbon 1,4-Dipoles:  Generation and [4 + 2] Annulation in the Formation of Carbo-/Heterocycles
    作者:Guozhu Zhang、Xiaogen Huang、Guotao Li、Liming Zhang
    DOI:10.1021/ja077948e
    日期:2008.2.1
    A novel concept of Au-containing all-carbon 1,n-dipoles is advanced. From 1-(1-alkynyl) cyclopropyl ketones, Au-containing all-carbon 1,4-dipoles are presumably generated in situ and can efficiently participate in [4 + 2] annulation with dipolarophiles including indoles, various carbonyl compounds, imines, and silyl enol ethers. Polycyclic, fully substituted furans are readily synthesized under mild reaction conditions.
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