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(E,E)-1,8-dibromocyclotetradeca-1,8-diene | 175286-47-2

中文名称
——
中文别名
——
英文名称
(E,E)-1,8-dibromocyclotetradeca-1,8-diene
英文别名
(1E,8E)-1,8-dibromocyclotetradeca-1,8-diene
(E,E)-1,8-dibromocyclotetradeca-1,8-diene化学式
CAS
175286-47-2
化学式
C14H22Br2
mdl
——
分子量
350.137
InChiKey
SIVLOJMEFYHWPC-IHJNGOQESA-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):
    6.5
  • 重原子数:
    16
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.71
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Doubly Bridged Biscyclopropenones, a New Family of Phanes
    摘要:
    The first representatives, 10-12, of the new species of double-decked cyclopropenonophanes were synthesized by cycloaddition reactions of dichlorocarbene to alkynylenecyclopropenonophanes 7-9 followed by hydrolysis as well as in an alternative route involving hydride abstraction from dichlorotricycloalkadienes 16 and 17 to dichlorocyclopropenyliophanes and in situ hydrolysis of the latter. The X-ray analysis of [3.3]cyclopropenonophane 10 reveals a considerable tetragonalization of the bridgehead carbon atoms, indicating a significant deformation of the cyclopropenone moieties in the phane corset, According to ab initio calculations, the it orbitals of the cyclopropenones display transannular interactions of nearly the same scale as found in 7.
    DOI:
    10.1021/jo9515539
  • 作为产物:
    描述:
    1,8-环十四二炔N-溴代丁二酰亚胺(NBS) 、 Schwartz's reagent 作用下, 生成 (E,E)-1,8-dibromocyclotetradeca-1,8-diene 、 (E,E)-1,9-dibromocyclotetradeca-1,8-diene
    参考文献:
    名称:
    Doubly Bridged Biscyclopropenones, a New Family of Phanes
    摘要:
    The first representatives, 10-12, of the new species of double-decked cyclopropenonophanes were synthesized by cycloaddition reactions of dichlorocarbene to alkynylenecyclopropenonophanes 7-9 followed by hydrolysis as well as in an alternative route involving hydride abstraction from dichlorotricycloalkadienes 16 and 17 to dichlorocyclopropenyliophanes and in situ hydrolysis of the latter. The X-ray analysis of [3.3]cyclopropenonophane 10 reveals a considerable tetragonalization of the bridgehead carbon atoms, indicating a significant deformation of the cyclopropenone moieties in the phane corset, According to ab initio calculations, the it orbitals of the cyclopropenones display transannular interactions of nearly the same scale as found in 7.
    DOI:
    10.1021/jo9515539
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文献信息

  • Doubly Bridged Biscyclopropenones, a New Family of Phanes
    作者:Rolf Gleiter、Martin Merger、Annegret Altreuther、Hermann Irngartinger
    DOI:10.1021/jo9515539
    日期:1996.1.1
    The first representatives, 10-12, of the new species of double-decked cyclopropenonophanes were synthesized by cycloaddition reactions of dichlorocarbene to alkynylenecyclopropenonophanes 7-9 followed by hydrolysis as well as in an alternative route involving hydride abstraction from dichlorotricycloalkadienes 16 and 17 to dichlorocyclopropenyliophanes and in situ hydrolysis of the latter. The X-ray analysis of [3.3]cyclopropenonophane 10 reveals a considerable tetragonalization of the bridgehead carbon atoms, indicating a significant deformation of the cyclopropenone moieties in the phane corset, According to ab initio calculations, the it orbitals of the cyclopropenones display transannular interactions of nearly the same scale as found in 7.
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