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phenanthridin-6-yldiphenylphosphine oxide | 1378043-01-6

中文名称
——
中文别名
——
英文名称
phenanthridin-6-yldiphenylphosphine oxide
英文别名
6-Diphenylphosphorylphenanthridine;6-diphenylphosphorylphenanthridine
phenanthridin-6-yldiphenylphosphine oxide化学式
CAS
1378043-01-6
化学式
C25H18NOP
mdl
——
分子量
379.398
InChiKey
HMOSTTIDGNKORC-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):
    5.9
  • 重原子数:
    28
  • 可旋转键数:
    3
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    30
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

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文献信息

  • Ni-catalyzed construction of C–P bonds from electron-deficient phenols via the in situ aryl C–O activation by PyBroP
    作者:Yu-Long Zhao、Guo-Jie Wu、Fu-She Han
    DOI:10.1039/c2cc31718d
    日期:——
    The C–P bond forming reaction using electron-deficient phenol substrates was considerably challenging. Herein, we present a new protocol that allows for one-pot construction of C–P bonds via the cross-coupling of phenols and phosphine oxide or phosphite in the presence of a nickel catalyst.
    使用缺电子酚类底物的C-P键形成反应相当具有挑战性。在此,我们提出一种新方案,通过在催化剂的作用下,实现酚类与膦氧化物或亚磷酸酯的一锅法交叉偶联,从而构建C-P键。
  • Visible-light-induced tandem radical addition–cyclization of 2-aryl phenyl isocyanides catalysed by recyclable covalent organic frameworks
    作者:Shuyang Liu、Wenna Pan、Songxiao Wu、Xiubin Bu、Shigang Xin、Jipan Yu、Hao Xu、Xiaobo Yang
    DOI:10.1039/c9gc00022d
    日期:——
    A visible-light-induced tandem radical addition–cyclization sequence via 2-aryl phenyl isocyanides as the starting material and two-dimensional covalent organic frameworks (2D-COFs) as the photocatalyst was developed, delivering multifarious 6-substituted phenanthridines in high yields. Benefitting from the utilization of a heterogeneous photocatalyst, this protocol features easy catalyst separation
    的可见光诱导的串联基加环化序列通过2 -芳基苯基异腈作为起始原料和二维共价有机骨架(2D-的COF)作为光催化剂的开发,以高收率提供繁杂6-取代菲啶。该协议得益于多相光催化剂的利用,具有易于分离催化剂和出色的可回收性的特点。多次运行后观察到的催化活性损失可忽略不计。连续流程实验进一步证明了该协议的高度实用性。
  • Selective P−C(sp<sup>3</sup> ) Bond Cleavage and Radical Alkynylation of α-Phosphorus Alcohols by Photoredox Catalysis
    作者:Kunfang Jia、Junzhao Li、Yiyun Chen
    DOI:10.1002/chem.201800202
    日期:2018.3.2
    cleavage and radical alkynylation of α‐phosphorus alcohols to construct phosphonoalkynes is reported. The phosphorus radical is generated upon P−C bond cleavage reaction via the alkoxyl radical through photoredox catalysis with cyclic iodine(III) reagents. Various arylphosphinoyl‐, alkylphosphinoyl‐, phosphonate‐, and phosphonic amide alcohols serve as radical phosphorus precursors to construct phosphonoalkynes
    本文报道了α-醇的第一次P-C(sp 3)键裂解和自由基炔基化反应,以构建膦炔基。自由基是通过环(III)试剂通过光氧化还原催化烷氧基进行P-C键裂解反应而生成的。各种芳基膦酰基,烷基膦酰基,膦酸酯和膦酰胺醇都作为自由基前体,首次构建了膦炔烃
  • Metal-Free Synthesis of 6-Phosphorylated Phenanthridines: Synthetic and Mechanistic Insights
    作者:Ludovik Noël-Duchesneau、Elodie Lagadic、Fabrice Morlet-Savary、Jean-François Lohier、Isabelle Chataigner、Martin Breugst、Jacques Lalevée、Annie-Claude Gaumont、Sami Lakhdar
    DOI:10.1021/acs.orglett.6b02983
    日期:2016.11.18
    the generation of phosphinoyl radicals from the combination of diphenyliodonium salt (Ph2I+,–OTf) with triethylamine (Et3N) in the presence of secondary phosphine oxides is reported. By employing this practical and simple approach, a large variety of 6-phosphorylated phenanthridines have been synthesized through the addition of phosphinoyl radicals to isonitriles as radical acceptors. The reaction works
    报道了在仲氧化膦的存在下,由二苯基鎓盐(Ph 2 I +,– OTf)与三乙胺(Et 3 N)结合生成膦酰基的新颖有效方法。通过采用这种实用且简单的方法,已经通过向膦腈中添加膦酰基作为自由基受体而合成了多种6-磷酸化的菲啶。在没有任何过渡属或光催化剂的情况下,该反应可顺利进行。在电子顺磁共振(EPR)和密度泛函理论(DFT)计算的基础上,讨论了该反应的机理。
  • Synthesis of phenanthridin-6-yldiphenylphosphine oxides by oxidative cyclization of 2-isocyanobiphenyls with diarylphosphine oxides
    作者:Yuewen Li、Guanyinsheng Qiu、Qiuping Ding、Jie Wu
    DOI:10.1016/j.tet.2014.05.039
    日期:2014.8
    A Mn(III)-promoted oxidative cyclization of 2-isocyanobiphenyls with diarylphosphine oxides is reported, providing phenanthridin-6-yldiphenylphosphine oxides in good yields. Radical phosphonation and isocyanide insertion are believed to be involved in the reaction process.
    据报道,Mn(III)以二芳基膦氧化物氧化了2-异氰基联苯的氧化环化反应,从而以高收率提供了菲啶-6-基二苯基膦氧化物。据信自由基膦酰化和异化物的插入与反应过程有关。
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