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(2-oxo-2H-chromen-4-yl)zinc bromide | 1330062-40-2

中文名称
——
中文别名
——
英文名称
(2-oxo-2H-chromen-4-yl)zinc bromide
英文别名
4-coumarinylzinc bromide
(2-oxo-2H-chromen-4-yl)zinc bromide化学式
CAS
1330062-40-2
化学式
C9H5BrO2Zn
mdl
——
分子量
290.431
InChiKey
MVPCHXMJMNXXLZ-UHFFFAOYSA-M
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):
    1.81
  • 重原子数:
    13.0
  • 可旋转键数:
    1.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    30.21
  • 氢给体数:
    0.0
  • 氢受体数:
    2.0

反应信息

  • 作为反应物:
    描述:
    (2-oxo-2H-chromen-4-yl)zinc bromide 作用下, 以 四氢呋喃 为溶剂, 以97%的产率得到4-iodocoumarin
    参考文献:
    名称:
    一种新型的有机锌试剂4-香豆素基溴化锌;取代香豆素衍生物的制备及其在合成中的应用
    摘要:
    通过将活性锌直接氧化加成到4-溴香豆素中,制得了一种新型的有机锌试剂溴化4-香豆素锌。所得的有机溴化锌与钯的各种芳基卤化物和酰氯进行交叉催化的交叉偶联反应,在温和的条件下以良好的收率得到相应的偶联产物。
    DOI:
    10.1016/j.tetlet.2011.03.151
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文献信息

  • [EN] FUNCTIONALIZED AZABORINE COMPOUNDS AND AZABORINE-CONTAINING BIARYLCARBOXAMIDES, AND COMPOSITIONS AND METHODS THEREOF<br/>[FR] COMPOSÉS D'AZABORINE FONCTIONNALISÉS ET BIARYLCARBOXAMIDES CONTENANT DE L'AZABORINE, ET LEURS COMPOSITIONS ET PROCÉDÉS
    申请人:TRUSTEES BOSTON COLLEGE
    公开号:WO2015160688A1
    公开(公告)日:2015-10-22
    The invention provides novel azaborine compounds, methods for their syntheses and functionalization, and various applications thereof. For example, novel azaborine-containing biarylcarboxylic acids and biarylcarboxamides are disclosed herein, which provide the opportunity to be used as therapeutic agents in different diseases. The novel azaborine-containing compounds show unique physical and biological properties when compared to their corresponding all-carbon compounds. Also, disclosed herein are substituted 1,2-dihydro- 1,2-azaborine compounds and methods for making the same including methods for the preparation of various substituted azaborines including alkyl, alkenyl, aryl, nitrile, heteroaryl, and fused ring substituents in the presence of B-H, B-Cl, B-O and N-H bonds from Br-substituted azaborines as well as the synthesis of new fused BN- heterocycles.
    本发明提供了新颖的氮因化合物、它们的合成及功能化方法,以及它们在各种应用中的用途。例如,本文公开了含有氮因的联芳基羧酸和联芳基酰胺,它们提供了作为不同疾病治疗剂使用的机会。与相应的全碳化合物相比,这些新颖的氮因化合物显示出独特的物理和生物学特性。此外,本文还公开了取代的1,2-二氢-1,2-氮因化合物及其制备方法,包括制备各种取代的氮因的方法,这些取代基包括烷基、烯基、芳基、腈、杂芳基和稠合环取代基,在B-H、B-Cl、B-O和N-H键的存在下,从取代的氮因出发,以及合成新的稠合BN杂环的方法。
  • Expanding the functional group tolerance of cross-coupling in 1,2-dihydro-1,2-azaborines: Installation of alkyl, alkenyl, aryl, and heteroaryl substituents while maintaining a B−H bond
    作者:Alec N. Brown、Bo Li、Shih-Yuan Liu
    DOI:10.1016/j.tet.2018.12.039
    日期:2019.2
    2-azaborine while maintaining the B-H functionality has been demonstrated. 17 examples, including dialkylzinc, alkyl-, alkenyl-, aryl-, as well as nitrogen-, sulfur-, and oxygen-containing heteroaryl-zinc halide reagents have been coupled to generate new C(3) substituted 1,2-azaborines in moderate to excellent yields.
    已经证明了催化的3-溴-1-(叔丁基二甲基甲硅烷基)-1,2-二氢-1,2-天竹碱的Negishi交叉偶联,同时保持了BH的功能性。17个实例,包括二烷基,烷基-,烯基-,芳基-以及含氮,和氧的杂芳基-卤化锌试剂已被偶联生成新的C(3)取代的1,2-氮杂硼烷中等至极好的产量。
  • FUNCTIONALIZED AZABORINE COMPOUNDS AND AZABORINE-CONTAINING BIARYLCARBOXAMIDES, AND COMPOSITIONS AND METHODS THEREOF
    申请人:The Trustees of Boston College
    公开号:US20170081347A1
    公开(公告)日:2017-03-23
    The invention provides novel azaborine compounds, methods for their syntheses and functionalization, and various applications thereof. For example, novel azaborine-containing biarylcarboxylic acids and biarylcarboxamides are disclosed herein, which provide the opportunity to be used as therapeutic agents in different diseases. The novel azaborine-containing compounds show unique physical and biological properties when compared to their corresponding all-carbon compounds. Also, disclosed herein are substituted 1,2-dihydro-1,2-azaborine compounds and methods for making the same including methods for the preparation of various substituted azaborines including alkyl, alkenyl, aryl, nitrile, heteroaryl, and fused ring substituents in the presence of B—H, B—Cl, B—O and N—H bonds from Br-substituted azaborines as well as the synthesis of new fused BN-heterocycles.
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