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[boranatodi(cyclohexyl)phosphino]cyclopentadiene | 1482501-57-4

中文名称
——
中文别名
——
英文名称
[boranatodi(cyclohexyl)phosphino]cyclopentadiene
英文别名
——
[boranatodi(cyclohexyl)phosphino]cyclopentadiene化学式
CAS
1482501-57-4
化学式
C17H30BP
mdl
——
分子量
276.21
InChiKey
WJUGKNICIXMUMJ-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:
    描述:
    [boranatodi(cyclohexyl)phosphino]cyclopentadiene 、 alkaline earth salt of/the/ methylsulfuric acid 在 正丁基锂 作用下, 以 四氢呋喃正己烷 为溶剂, 反应 19.0h, 以81%的产率得到
    参考文献:
    名称:
    An Active, General, and Long-Lived Palladium Catalyst for Cross-Couplings of Deactivated (Hetero)aryl Chlorides and Bromides with Arylboronic Acids
    摘要:
    An active, general, and long-lived palladium catalyst for Suzuki-Miyaura reactions of aryl and heteroaryl chlorides deactivated by steric hindrance, electron richness, and coordinating functional groups is reported. In reactions of arylbromide bearing two o-tert-butyl substituents, C(sp(3))-H arylation of the tert-butyl group, rather than the Suzuki-Miyaura reaction, proceeded in excellent yield. The key to the success of the reactions was the development of biphenylene-substituted dicyclohexylruthenocenylphosphine (CyR-Phos) as a supporting ligand.
    DOI:
    10.1021/jo402089r
  • 作为产物:
    描述:
    Dicyclohexyl(cyclopenta-1,3-dien-1-yl)phosphane 、 diborane(6)四氢呋喃 为溶剂, 反应 0.5h, 以573.9 mg的产率得到[boranatodi(cyclohexyl)phosphino]cyclopentadiene
    参考文献:
    名称:
    An Active, General, and Long-Lived Palladium Catalyst for Cross-Couplings of Deactivated (Hetero)aryl Chlorides and Bromides with Arylboronic Acids
    摘要:
    An active, general, and long-lived palladium catalyst for Suzuki-Miyaura reactions of aryl and heteroaryl chlorides deactivated by steric hindrance, electron richness, and coordinating functional groups is reported. In reactions of arylbromide bearing two o-tert-butyl substituents, C(sp(3))-H arylation of the tert-butyl group, rather than the Suzuki-Miyaura reaction, proceeded in excellent yield. The key to the success of the reactions was the development of biphenylene-substituted dicyclohexylruthenocenylphosphine (CyR-Phos) as a supporting ligand.
    DOI:
    10.1021/jo402089r
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