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2-ferrocenyloxy-4-methyl-1,3,2-dioxaphosphane | 418806-71-0

中文名称
——
中文别名
——
英文名称
2-ferrocenyloxy-4-methyl-1,3,2-dioxaphosphane
英文别名
——
2-ferrocenyloxy-4-methyl-1,3,2-dioxaphosphane化学式
CAS
418806-71-0
化学式
C14H17FeO3P
mdl
——
分子量
320.108
InChiKey
XLDWSVQKLDGFGK-WEWGPFMHSA-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:
    描述:
    参考文献:
    名称:
    Hydroxyferrocene as a prochiral analog of phenols: cyclopalladation of a mixed phosphite ester of hydroxyferrocene
    摘要:
    Hydroxyferrocene (ferrocenol), a metallocene analog of phenol, has been converted into a phosphite ester with chiral (racemic) butane-1,3-diol which undergoes cyclopalladation similarly to hydroxyarene phosphites. In this case, a planar chirality emerges but no diastereoselectivity has been observed. The molecular structure of the cyclopalladated product as pyridine add-act has been established by the X-ray study of a single crystal. (C) 2002 Elsevier Science B.V. All rights reserved.
    DOI:
    10.1016/s0022-328x(01)01228-1
  • 作为产物:
    描述:
    ferrocenol 、 2-Chloro-4-methyl-1,3,2-dioxaphosphorinane 在 Et3N 作用下, 以 四氢呋喃 为溶剂, 以81.7%的产率得到2-ferrocenyloxy-4-methyl-1,3,2-dioxaphosphane
    参考文献:
    名称:
    Hydroxyferrocene as a prochiral analog of phenols: cyclopalladation of a mixed phosphite ester of hydroxyferrocene
    摘要:
    Hydroxyferrocene (ferrocenol), a metallocene analog of phenol, has been converted into a phosphite ester with chiral (racemic) butane-1,3-diol which undergoes cyclopalladation similarly to hydroxyarene phosphites. In this case, a planar chirality emerges but no diastereoselectivity has been observed. The molecular structure of the cyclopalladated product as pyridine add-act has been established by the X-ray study of a single crystal. (C) 2002 Elsevier Science B.V. All rights reserved.
    DOI:
    10.1016/s0022-328x(01)01228-1
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