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[4-[Tert-butyl(dimethyl)silyl]oxyphenyl]-pyridin-2-ylmethanone

中文名称
——
中文别名
——
英文名称
[4-[Tert-butyl(dimethyl)silyl]oxyphenyl]-pyridin-2-ylmethanone
英文别名
——
[4-[Tert-butyl(dimethyl)silyl]oxyphenyl]-pyridin-2-ylmethanone化学式
CAS
——
化学式
C18H23NO2Si
mdl
——
分子量
313.472
InChiKey
CFPKFANJWIEURV-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):
    4.7
  • 重原子数:
    22
  • 可旋转键数:
    5
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    39.2
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    2-溴吡啶ethyl (4-tert-butyldimethylsilyloxyphenyl)glyoxylate正丁基锂 作用下, 以 四氢呋喃正己烷 为溶剂, 以50%的产率得到Di(2-pyridyl)<4-((tert-butyldimethylsilyl)oxy)phenyl>methanol
    参考文献:
    名称:
    Preparation of Dipyridylmethane Ligands with Pseudo-C2 Symmetry. Grafting on Polystyrenes via Transformation to Phenolic Derivatives
    摘要:
    Efficient grafting of dipyridylmethane ligands on highly cross-linked as well as gel-type chloromethylated polystyrenes has been achieved using phenolic derivatives of the ligands. In this way, chiral polymer-supported ligands with pseudo-C-2 symmetry were obtained. The synthesis of the ligands and their grafting under mild conditions are described, as well as the preparation of monomeric models. During reduction of 6,6'-(2,2-dimethyl-1-oxopropyl) derivatives with sodium borohydride, the R,S isomers were unexpectedly formed with high selectivity.
    DOI:
    10.1021/jo00111a038
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文献信息

  • Preparation of Dipyridylmethane Ligands with Pseudo-C2 Symmetry. Grafting on Polystyrenes via Transformation to Phenolic Derivatives
    作者:Vincent Levacher、Christina Moberg
    DOI:10.1021/jo00111a038
    日期:1995.3
    Efficient grafting of dipyridylmethane ligands on highly cross-linked as well as gel-type chloromethylated polystyrenes has been achieved using phenolic derivatives of the ligands. In this way, chiral polymer-supported ligands with pseudo-C-2 symmetry were obtained. The synthesis of the ligands and their grafting under mild conditions are described, as well as the preparation of monomeric models. During reduction of 6,6'-(2,2-dimethyl-1-oxopropyl) derivatives with sodium borohydride, the R,S isomers were unexpectedly formed with high selectivity.
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