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3-bicymantrenylcarbinol | 193225-94-4

中文名称
——
中文别名
——
英文名称
3-bicymantrenylcarbinol
英文别名
——
3-bicymantrenylcarbinol化学式
CAS
193225-94-4
化学式
C17H10Mn2O7
mdl
——
分子量
436.138
InChiKey
WOFFUNMEGJHOJV-UHFFFAOYSA-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):
    None
  • 重原子数:
    None
  • 可旋转键数:
    None
  • 环数:
    None
  • sp3杂化的碳原子比例:
    None
  • 拓扑面积:
    None
  • 氢给体数:
    None
  • 氢受体数:
    None

反应信息

  • 作为反应物:
    描述:
    3-bicymantrenylcarbinol 在 Et3SiH 、 CF3COOH 作用下, 以 氯仿 为溶剂, 生成
    参考文献:
    名称:
    Bicymantrenyl chemistry
    摘要:
    Planar chiral 2- and 3-bicymantrenylcarbaldehydes can be resolved to enantiomers through Schiff's bases with (S)-(-)-alpha-phenylethylamine. Optically active derivatives of bicymantrenyl with Me and CH2OH substituents were synthesized from (-)-3-bicymantrenylcarbaldehyde. The absolute configuration. of Schiff's base obtained from (+)-3-bicymantrenylcarbaldehyde was determined by X-ray diffraction analysis.
    DOI:
    10.1007/bf02495365
  • 作为产物:
    描述:
    3-bicymantrenylaldehyde 在 NaBH4 作用下, 以 乙醇 为溶剂, 以91%的产率得到3-bicymantrenylcarbinol
    参考文献:
    名称:
    Bicymantrenyl chemistry
    摘要:
    Planar chiral 2- and 3-bicymantrenylcarbaldehydes can be resolved to enantiomers through Schiff's bases with (S)-(-)-alpha-phenylethylamine. Optically active derivatives of bicymantrenyl with Me and CH2OH substituents were synthesized from (-)-3-bicymantrenylcarbaldehyde. The absolute configuration. of Schiff's base obtained from (+)-3-bicymantrenylcarbaldehyde was determined by X-ray diffraction analysis.
    DOI:
    10.1007/bf02495365
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文献信息

  • Metallation of bicymantrenyl and synthesis of polycymantrenyls
    作者:A.G. Ginzburg、S.V. Suprunovich、F.M. Dolgushin、A.I. Yanovsky、E.V. Vorontsov、V.I. Sokolov
    DOI:10.1016/s0022-328x(96)06556-4
    日期:1997.5
    Bicymantrenyl, eta(5),eta(5)-C10H8[Mn(CO)(3)](2) (1), may be metallated at the Cp-ring with BuLi (THF, -60 degrees C) to give monolithium (2) and polylithium derivatives. Metallation of 1 proceeds concurrently on both alpha- and beta- positions, the beta-substitution product being predominant. A number of derivatives of 1 with substituents R = D, COOH, CHO, PPh2 have been synthesized in the reactions of monolithium derivative 2 with different electrophiles (D2O, CO2, DMFA, Ph2PCl respectively). Under the action of CuCl2 the oxidative coupling of 2 proceeds to give tetracymantrenyl (11a). Oxidative coupling of a mixture of 2 with cymantrenyllithium affords two isomers of tricymantrenyl (12a, 12b). The structures of 11a, 12a, 12b were established by an X-ray study. (C) 1997 Elsevier Science S.A.
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