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[(η5;η1-C5H4CH(OPPh2)C6H5)Fe(CO)CH3] | 476314-31-5

中文名称
——
中文别名
——
英文名称
[(η5;η1-C5H4CH(OPPh2)C6H5)Fe(CO)CH3]
英文别名
——
[(η5;η1-C5H4CH(OPPh2)C6H5)Fe(CO)CH3]化学式
CAS
476314-31-5;476170-19-1
化学式
C26H23FeO2P
mdl
——
分子量
454.288
InChiKey
QLHVPLIRWCUULZ-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

  • 作为反应物:
    参考文献:
    名称:
    Synthesis of a new iron Lewis acid catalyst possessing a chelating cyclopentadienyldiphenylphosphinite ligand, (η5:η1-C5H4CH(Ph)OPPh2)
    摘要:
    A new iron Lewis acid catalyst, [(eta(5):eta(1)-C5H4CH(Ph)OPPh2)Fe(CO)(THF)](+)[BF4](-) featuring a cyclopentadienyl ring that is tethered to a terminal diphenylphosphinite moiety was created. This is the first complex to contain a chelating eta(5):eta(1)-cyclopentadienyl-phosphinite ligand. This new racemic iron Lewis acid was tested and found to be an effective catalyst in an aziridine-forming reaction. An asymmetric alcohol that is a precursor of the chiral catalyst was synthesized with greater than 95% ee. Upon ligation of the diphenylphosphinite to the iron center, a 3:2 mixture of diastereomers was formed. The diastereomeric mixture of the asymmetric catalysts was utilized in the aziridine-forming reaction and produced the cis-aziridine with low enantiomeric excess. (C) 2002 Elsevier Science B.V. All rights reserved.
    DOI:
    10.1016/s0022-328x(02)01257-3
  • 作为产物:
    参考文献:
    名称:
    Synthesis of a new iron Lewis acid catalyst possessing a chelating cyclopentadienyldiphenylphosphinite ligand, (η5:η1-C5H4CH(Ph)OPPh2)
    摘要:
    A new iron Lewis acid catalyst, [(eta(5):eta(1)-C5H4CH(Ph)OPPh2)Fe(CO)(THF)](+)[BF4](-) featuring a cyclopentadienyl ring that is tethered to a terminal diphenylphosphinite moiety was created. This is the first complex to contain a chelating eta(5):eta(1)-cyclopentadienyl-phosphinite ligand. This new racemic iron Lewis acid was tested and found to be an effective catalyst in an aziridine-forming reaction. An asymmetric alcohol that is a precursor of the chiral catalyst was synthesized with greater than 95% ee. Upon ligation of the diphenylphosphinite to the iron center, a 3:2 mixture of diastereomers was formed. The diastereomeric mixture of the asymmetric catalysts was utilized in the aziridine-forming reaction and produced the cis-aziridine with low enantiomeric excess. (C) 2002 Elsevier Science B.V. All rights reserved.
    DOI:
    10.1016/s0022-328x(02)01257-3
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