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(E)-1-(Benzyloxy)-5-(2-phenylethyl)-2,6-heptadiene | 215386-07-5

中文名称
——
中文别名
——
英文名称
(E)-1-(Benzyloxy)-5-(2-phenylethyl)-2,6-heptadiene
英文别名
——
(E)-1-(Benzyloxy)-5-(2-phenylethyl)-2,6-heptadiene化学式
CAS
215386-07-5
化学式
C22H26O
mdl
——
分子量
306.448
InChiKey
LVSSZGKTRUAPJV-MDZDMXLPSA-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):
    5.58
  • 重原子数:
    23.0
  • 可旋转键数:
    10.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.27
  • 拓扑面积:
    9.23
  • 氢给体数:
    0.0
  • 氢受体数:
    1.0

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Catalytic Iron-Mediated Triene Carbocyclizations: Stereoselective Five-Membered Ring Forming Carbocyclizations
    摘要:
    The full details of investigations into the regiochemistry and stereochemistry of iron-catalyzed carbocyclizations of 2,7,9-decatriene derivatives to form five-membered carbocyclic ring systems are described. The roles of the allylic substituent, the alkene geometry, diene substitution, and the influence of resident stereogenic centers incorporated in the tether chain connecting the reacting 1,3-diene and alkene subunits are discussed.
    DOI:
    10.1021/jo00102a016
  • 作为产物:
    参考文献:
    名称:
    Catalytic Iron-Mediated Triene Carbocyclizations: Stereoselective Five-Membered Ring Forming Carbocyclizations
    摘要:
    The full details of investigations into the regiochemistry and stereochemistry of iron-catalyzed carbocyclizations of 2,7,9-decatriene derivatives to form five-membered carbocyclic ring systems are described. The roles of the allylic substituent, the alkene geometry, diene substitution, and the influence of resident stereogenic centers incorporated in the tether chain connecting the reacting 1,3-diene and alkene subunits are discussed.
    DOI:
    10.1021/jo00102a016
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