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ditert-butyl-(4-methoxyphenoxy)silane

中文名称
——
中文别名
——
英文名称
ditert-butyl-(4-methoxyphenoxy)silane
英文别名
——
ditert-butyl-(4-methoxyphenoxy)silane化学式
CAS
——
化学式
C15H26O2Si
mdl
——
分子量
266.456
InChiKey
RSECQFSZNLIKQF-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):
    4.4
  • 重原子数:
    18.0
  • 可旋转键数:
    3.0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.6
  • 拓扑面积:
    18.46
  • 氢给体数:
    0.0
  • 氢受体数:
    2.0

反应信息

  • 作为反应物:
    描述:
    ditert-butyl-(4-methoxyphenoxy)silaneN-溴代丁二酰亚胺(NBS) 、 sodium hydroxide 作用下, 以 二氯甲烷N,N-二甲基甲酰胺 为溶剂, 生成 Ditert-butyl-hydroxy-(4-methoxyphenoxy)silane
    参考文献:
    名称:
    Silanol: A Traceless Directing Group for Pd-Catalyzed o-Alkenylation of Phenols
    摘要:
    A silanol-directed, Pd(II)-catalyzed C-H alkenylation of phenols is reported. This work features silanol, as a novel traceless directing group, and a directed o-C-H alkenylation of phenols. This new method allows for efficient synthesis of diverse alkenylated phenols, including an estrone derivative.
    DOI:
    10.1021/ja204924j
  • 作为产物:
    参考文献:
    名称:
    Silanol: A Traceless Directing Group for Pd-Catalyzed o-Alkenylation of Phenols
    摘要:
    A silanol-directed, Pd(II)-catalyzed C-H alkenylation of phenols is reported. This work features silanol, as a novel traceless directing group, and a directed o-C-H alkenylation of phenols. This new method allows for efficient synthesis of diverse alkenylated phenols, including an estrone derivative.
    DOI:
    10.1021/ja204924j
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文献信息

  • Silanol: A Traceless Directing Group for Pd-Catalyzed <i>o</i>-Alkenylation of Phenols
    作者:Chunhui Huang、Buddhadeb Chattopadhyay、Vladimir Gevorgyan
    DOI:10.1021/ja204924j
    日期:2011.8.17
    A silanol-directed, Pd(II)-catalyzed C-H alkenylation of phenols is reported. This work features silanol, as a novel traceless directing group, and a directed o-C-H alkenylation of phenols. This new method allows for efficient synthesis of diverse alkenylated phenols, including an estrone derivative.
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