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(6S,7R)-6,7-Dihydroxy-tricyclo[10.3.3.01,12]octadecane-14,17-dione | 162251-45-8

中文名称
——
中文别名
——
英文名称
(6S,7R)-6,7-Dihydroxy-tricyclo[10.3.3.01,12]octadecane-14,17-dione
英文别名
(6R,7S)-6,7-dihydroxytricyclo[10.3.3.01,12]octadecane-14,17-dione
(6S,7R)-6,7-Dihydroxy-tricyclo[10.3.3.0<sup>1,12</sup>]octadecane-14,17-dione化学式
CAS
162251-45-8
化学式
C18H28O4
mdl
——
分子量
308.418
InChiKey
FYIHVWLFRXVZFI-OQSMONGASA-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):
    1.5
  • 重原子数:
    22
  • 可旋转键数:
    0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.89
  • 拓扑面积:
    74.6
  • 氢给体数:
    2
  • 氢受体数:
    4

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    (6S,7R)-6,7-Dihydroxy-tricyclo[10.3.3.01,12]octadecane-14,17-dione 在 lithium aluminium tetrahydride 、 sodium hydride 、 对甲苯磺酸 作用下, 以 四氢呋喃 为溶剂, 反应 37.25h, 生成 4,5,6,7,10,11,12,13-octahydro-3a,13a-propeno-1H-cyclopentacyclodecene-8,9-dione
    参考文献:
    名称:
    Weiss-Cook Condensations Involving Unsaturated and Transannularly Alkylated Cyclododecane-1,2-diones
    摘要:
    (Z)-Cyclododec-7-ene-1,2-dione (4), its alkyne equivalent 7, and the structurally related propellane 14 have been subjected to condensation with dimethyl 1,3-acetonedicarboxylate. The alpha-diketones 4 and 7 undergo the Weiss-Cook condensation normally to deliver diquinane products in high yield. The sterically congested 14 showed no tendency to react. The underlying cause of the parallelism between eight- and twelve-membered rings and the contrasting behavior of cyclodecyl analogs is evaluated in terms of thermodynamic versus kinetic control.
    DOI:
    10.1021/jo00107a013
  • 作为产物:
    描述:
    tricyclo<10.3.3.01,12>octadec-6-ene-14,17-dione四氧化锇N-甲基吗啉氧化物 作用下, 以 四氢呋喃叔丁醇 为溶剂, 反应 216.0h, 以77%的产率得到(6S,7R)-6,7-Dihydroxy-tricyclo[10.3.3.01,12]octadecane-14,17-dione
    参考文献:
    名称:
    Weiss-Cook Condensations Involving Unsaturated and Transannularly Alkylated Cyclododecane-1,2-diones
    摘要:
    (Z)-Cyclododec-7-ene-1,2-dione (4), its alkyne equivalent 7, and the structurally related propellane 14 have been subjected to condensation with dimethyl 1,3-acetonedicarboxylate. The alpha-diketones 4 and 7 undergo the Weiss-Cook condensation normally to deliver diquinane products in high yield. The sterically congested 14 showed no tendency to react. The underlying cause of the parallelism between eight- and twelve-membered rings and the contrasting behavior of cyclodecyl analogs is evaluated in terms of thermodynamic versus kinetic control.
    DOI:
    10.1021/jo00107a013
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文献信息

  • Weiss-Cook Condensations Involving Unsaturated and Transannularly Alkylated Cyclododecane-1,2-diones
    作者:Heiner Detert、James C. Lanter、Leo A. Paquette
    DOI:10.1021/jo00107a013
    日期:1995.1
    (Z)-Cyclododec-7-ene-1,2-dione (4), its alkyne equivalent 7, and the structurally related propellane 14 have been subjected to condensation with dimethyl 1,3-acetonedicarboxylate. The alpha-diketones 4 and 7 undergo the Weiss-Cook condensation normally to deliver diquinane products in high yield. The sterically congested 14 showed no tendency to react. The underlying cause of the parallelism between eight- and twelve-membered rings and the contrasting behavior of cyclodecyl analogs is evaluated in terms of thermodynamic versus kinetic control.
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