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1,4-anti-5-methyl-1,4-diphenyl-6-heptene-1,4-diol

中文名称
——
中文别名
——
英文名称
1,4-anti-5-methyl-1,4-diphenyl-6-heptene-1,4-diol
英文别名
(1R,4S,5S)-5-methyl-1,4-diphenylhept-6-ene-1,4-diol
1,4-anti-5-methyl-1,4-diphenyl-6-heptene-1,4-diol化学式
CAS
——
化学式
C20H24O2
mdl
——
分子量
296.409
InChiKey
BNOUZSNGWWJRHO-DBVUQKKJSA-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):
    3.9
  • 重原子数:
    22
  • 可旋转键数:
    7
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.3
  • 拓扑面积:
    40.5
  • 氢给体数:
    2
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    溴丁基-镁1,2-联苯甲酰乙烷二氯二茂锆 作用下, 以 四氢呋喃 为溶剂, 反应 5.5h, 以17%的产率得到1,4-二(苯基)丁烷-1,4-二醇
    参考文献:
    名称:
    Transformation of Zirconocene−Olefin Complexes into Zirconocene Allyl Hydride and Their Use as Dual Nucleophilic Reagents:  Reactions with Acid Chloride and 1,4-Diketone
    摘要:
    Zirconocene-olefin complexes Cp2Zr(H2C=CHR), prepared in benzene-THF at 0 degreesC, react with acid chlorides to provide homoallylic alcohols. The key is an equilibrium between the zirconocene-olefin complexes and the corresponding zirconocene allyl hydride complexes via allylic C-H bond cleavage of the coordinating alkenes. Furthermore, the zirconocene-olefin complexes are also available for the reaction with 1,4-diketone to afford anti-1,4-diols with excellent diastereoselectivity. Thus, Cp2Zr(H2C CHR) serves as a donor of both hydride and an allylic group. These reactions also proceed efficiently by using zirconocene-olefin complexes, derived from Cp2ZrCl2, Mg metal, and 1-alkenes.
    DOI:
    10.1021/ja049184y
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文献信息

  • Transformation of Zirconocene−Olefin Complexes into Zirconocene Allyl Hydride and Their Use as Dual Nucleophilic Reagents:  Reactions with Acid Chloride and 1,4-Diketone
    作者:Kazuya Fujita、Hideki Yorimitsu、Hiroshi Shinokubo、Koichiro Oshima
    DOI:10.1021/ja049184y
    日期:2004.6.1
    Zirconocene-olefin complexes Cp2Zr(H2C=CHR), prepared in benzene-THF at 0 degreesC, react with acid chlorides to provide homoallylic alcohols. The key is an equilibrium between the zirconocene-olefin complexes and the corresponding zirconocene allyl hydride complexes via allylic C-H bond cleavage of the coordinating alkenes. Furthermore, the zirconocene-olefin complexes are also available for the reaction with 1,4-diketone to afford anti-1,4-diols with excellent diastereoselectivity. Thus, Cp2Zr(H2C CHR) serves as a donor of both hydride and an allylic group. These reactions also proceed efficiently by using zirconocene-olefin complexes, derived from Cp2ZrCl2, Mg metal, and 1-alkenes.
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