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[(dippe)Ni(η2-C,O-phthalimide)] | 1432726-49-2

中文名称
——
中文别名
——
英文名称
[(dippe)Ni(η2-C,O-phthalimide)]
英文别名
[(dippe)Ni(η2-C,O-phthalimide)]
[(dippe)Ni(η2-C,O-phthalimide)]化学式
CAS
1432726-49-2
化学式
C22H37NNiO2P2
mdl
——
分子量
468.179
InChiKey
QPMGQZGDAWQINW-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):
    None
  • 重原子数:
    None
  • 可旋转键数:
    None
  • 环数:
    None
  • sp3杂化的碳原子比例:
    None
  • 拓扑面积:
    None
  • 氢给体数:
    None
  • 氢受体数:
    None

反应信息

  • 作为产物:
    参考文献:
    名称:
    Selective C═O Reduction in Phthalimide with Nickel(0) Compounds
    摘要:
    The catalytic reduction of phthalimide was achieved using nickel catalysts. The use of catalytic amounts (20% mol) of [Ni(COD)(2)] or [(dippe)Ni(mu-H)](2) (1) allowed the monoreduction of phthalimide to yield isoindolinone and benzamide, at 140-180 degrees C and 750 psi of H-2. When the N-H moiety of phthalimide was protected with a trimethylsilyl group, both C=O groups were reduced to yield (trimethylsilyl)isoindoline. However, when a methyl moiety was used as the protecting group, the C=O groups and the aromatic ring were reduced, using rather similar reaction conditions, due to the formation of 5 angstrom (average) nickel nanoparticles.
    DOI:
    10.1021/om400164g
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同类化合物

相关结构分类