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(R)-(η(5)-1-hydroxydiphenylmethyl-2-methyl-4-phenylcyclopentadienyl)di(carbonyl)methylsulfonyliron | 239468-54-3

中文名称
——
中文别名
——
英文名称
(R)-(η(5)-1-hydroxydiphenylmethyl-2-methyl-4-phenylcyclopentadienyl)di(carbonyl)methylsulfonyliron
英文别名
(S)-(η(5)-1-hydroxydiphenylmethyl-2-methyl-4-phenylcyclopentadienyl)di(carbonyl)methylsulfonyliron
(R)-(η(5)-1-hydroxydiphenylmethyl-2-methyl-4-phenylcyclopentadienyl)di(carbonyl)methylsulfonyliron化学式
CAS
239468-54-3;239477-46-4
化学式
C28H24FeO5S
mdl
——
分子量
528.409
InChiKey
XJKFSMHPYWKTID-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:
    描述:
    (S)-(η(5)-1-hydroxydiphenylmethyl-2-methyl-4-phenylcyclopentadienyl)di(carbonyl)methyliron二氧化硫二氧化硫 为溶剂, 以91%的产率得到(R)-(η(5)-1-hydroxydiphenylmethyl-2-methyl-4-phenylcyclopentadienyl)di(carbonyl)methylsulfonyliron
    参考文献:
    名称:
    Synthesis and Characterization of Planar-Chiral Cyclopentadienyliron Complexes (S)- and (R)-{η5-[1-Ph2(OH)C-2-Me-4-PhC5H2]}Fe(CO)2R (R = C⋮CPh, Me, SO2Me)
    摘要:
    The first enantiomerically pure planar-chiral cyclopentadienyliron complexes, (S)- and (R)-eta(5)-(CpFe)-Fe-c(CO)(2)R [Cp-c = 1-hydroxydiphenylmethyl-2-methyl-4-phenylcyclopentadienyl; R = C=CPh (6), Me (8)], in which the locus of chirality is in the cyclopentadienyl center, were synthesized from (CpFe)-Fe-a(CO)(2)I (4a: Cp-a = 1-(-)-menthoxycarbonyl-2-methyl-4-phenylcyclopentadienyl) and (CpFe)-Fe-b(CO)(2)I (4b: Cp-b = 1-(+)-menthoxycarbonyl-2-methyl-4-phenylcyclopentadienyl) and were isolated as a diastereomerically pure form by fractional recrystallization. The molecular structures of 4a and 4b, including the absolute configuration, have been established by an X-ray crystallographic analysis based on the configuration of the (-)- and (+)-menthyl groups.
    DOI:
    10.1021/om9810347
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