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(2R,3S)-2,3-dimethyl-2-((4-methylfuran-3-yl)methyl)cyclohexanone | 1436393-52-0

中文名称
——
中文别名
——
英文名称
(2R,3S)-2,3-dimethyl-2-((4-methylfuran-3-yl)methyl)cyclohexanone
英文别名
(2R,3S)-2,3-dimethyl-2-[(4-methylfuran-3-yl)methyl]cyclohexan-1-one
(2R,3S)-2,3-dimethyl-2-((4-methylfuran-3-yl)methyl)cyclohexanone化学式
CAS
1436393-52-0
化学式
C14H20O2
mdl
——
分子量
220.312
InChiKey
YJYZWRGXUVSZCA-SMDDNHRTSA-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

物化性质

  • 沸点:
    304.5±22.0 °C(predicted)
  • 密度:
    1.007±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.2
  • 重原子数:
    16
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.64
  • 拓扑面积:
    30.2
  • 氢给体数:
    0
  • 氢受体数:
    2

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

反应信息

  • 作为反应物:
    描述:
    (2R,3S)-2,3-dimethyl-2-((4-methylfuran-3-yl)methyl)cyclohexanone2,4,6-三异丙基苯磺酰基肼溶剂黄146 作用下, 以 乙醇 为溶剂, 反应 21.0h, 以29%的产率得到(2R,3S)-2,3-dimethyl-2-((4-methylfuran-3-yl)methyl)cyclohexanone azine
    参考文献:
    名称:
    An Enantioselective Approach to Furanoeremophilanes: (+)-9-Oxoeuryopsin
    摘要:
    An enantioselective total synthesis of the furanoeremophilane sesquiterpene (+)-9-oxoeuryopsin 1 is reported. The synthesis involves as a key step a copper(II) triflate catalyzed tandem asymmetric conjugate addition of AlMe3 to 2-methyl-2-cyclohexen-1-one with the Feringa (S,R,R)-phosphoramidite binaphthol ligand, followed by aldol condensation of the resulting aluminum enolate with 4-methyl-3-furaldehyde 4. This tandem transformation has not been previously reported with a 2-substituted-2-cyclohexen-1-one. Conventional functional group manipulations completed the synthesis.
    DOI:
    10.1021/jo400399q
  • 作为产物:
    参考文献:
    名称:
    An Enantioselective Approach to Furanoeremophilanes: (+)-9-Oxoeuryopsin
    摘要:
    An enantioselective total synthesis of the furanoeremophilane sesquiterpene (+)-9-oxoeuryopsin 1 is reported. The synthesis involves as a key step a copper(II) triflate catalyzed tandem asymmetric conjugate addition of AlMe3 to 2-methyl-2-cyclohexen-1-one with the Feringa (S,R,R)-phosphoramidite binaphthol ligand, followed by aldol condensation of the resulting aluminum enolate with 4-methyl-3-furaldehyde 4. This tandem transformation has not been previously reported with a 2-substituted-2-cyclohexen-1-one. Conventional functional group manipulations completed the synthesis.
    DOI:
    10.1021/jo400399q
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