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4-((S,E)-1-((2S,3R)-3-phenethylaziridin-2-yl)-3-phenylallyl)morpholine

中文名称
——
中文别名
——
英文名称
4-((S,E)-1-((2S,3R)-3-phenethylaziridin-2-yl)-3-phenylallyl)morpholine
英文别名
——
4-((S,E)-1-((2S,3R)-3-phenethylaziridin-2-yl)-3-phenylallyl)morpholine化学式
CAS
——
化学式
C23H28N2O
mdl
——
分子量
348.488
InChiKey
VPBFMZCVWSMZCP-OYNUIGCNSA-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):
    3.37
  • 重原子数:
    26.0
  • 可旋转键数:
    7.0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.39
  • 拓扑面积:
    34.41
  • 氢给体数:
    1.0
  • 氢受体数:
    3.0

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Stereocontrolled Synthesis of 1,2- and 1,3-Diamine Building Blocks from Aziridine Aldehyde Dimers
    摘要:
    Vicinal aziridine-containing diamines have been obtained with high syn-stereoselectivity from readily available aziridine aldehyde dimers in the Petasis borono-Mannich reaction. Subsequent solvent- and/or nucleophile-dependent ring-opening of the aziridine ring yields functionalized 1,2- and 1,3-diamines with high regioselectivity. The ring opening is also influenced by the substitution at the C3 position of the aziridine. A mechanistic rationale for the highly syn-selective three-component reaction is proposed.
    DOI:
    10.1021/jo401489q
  • 作为产物:
    描述:
    吗啉 、 、 反式-BETA-苯乙烯硼酸 反应 4.0h, 以56%的产率得到4-((S,E)-1-((2S,3R)-3-phenethylaziridin-2-yl)-3-phenylallyl)morpholine
    参考文献:
    名称:
    Stereocontrolled Synthesis of 1,2- and 1,3-Diamine Building Blocks from Aziridine Aldehyde Dimers
    摘要:
    Vicinal aziridine-containing diamines have been obtained with high syn-stereoselectivity from readily available aziridine aldehyde dimers in the Petasis borono-Mannich reaction. Subsequent solvent- and/or nucleophile-dependent ring-opening of the aziridine ring yields functionalized 1,2- and 1,3-diamines with high regioselectivity. The ring opening is also influenced by the substitution at the C3 position of the aziridine. A mechanistic rationale for the highly syn-selective three-component reaction is proposed.
    DOI:
    10.1021/jo401489q
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文献信息

  • Stereocontrolled Synthesis of 1,2- and 1,3-Diamine Building Blocks from Aziridine Aldehyde Dimers
    作者:Sean K. Liew、Zhi He、Jeffrey D. St. Denis、Andrei K. Yudin
    DOI:10.1021/jo401489q
    日期:2013.12.6
    Vicinal aziridine-containing diamines have been obtained with high syn-stereoselectivity from readily available aziridine aldehyde dimers in the Petasis borono-Mannich reaction. Subsequent solvent- and/or nucleophile-dependent ring-opening of the aziridine ring yields functionalized 1,2- and 1,3-diamines with high regioselectivity. The ring opening is also influenced by the substitution at the C3 position of the aziridine. A mechanistic rationale for the highly syn-selective three-component reaction is proposed.
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