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| 1187830-35-8

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
1187830-35-8
化学式
C15H23NO6
mdl
——
分子量
313.351
InChiKey
FAEFPTSSIOLBCE-QZOBBIQNSA-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):
    -1.41
  • 重原子数:
    22.0
  • 可旋转键数:
    5.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.6
  • 拓扑面积:
    111.41
  • 氢给体数:
    5.0
  • 氢受体数:
    7.0

反应信息

  • 作为反应物:
    描述:
    在 palladium 10% on activated carbon 、 甲酸铵 作用下, 以 甲醇 为溶剂, 反应 4.0h, 生成
    参考文献:
    名称:
    Access to Ring-Expanded Analogues of 2-Amino Sugars
    摘要:
    Ring-expanded 2-N-acetylamino sugar analogs Of D-glucose, D-galactose, and D-mannose have been prepared by a new synthetic route. Aspects of the highly substituted (x-amino aldehyde intermediates made them central to the approach, First, they were accessed via diastereoselective addition of a vinyl Grignard onto protected glycosyl amines. Also, the sterics of the bis-protected amine favored the formation of only one glycoside anomer. The new analogues reported here should prove useful in the development of tools to investigate the role of 2-amino sugars in biology.
    DOI:
    10.1021/ol9018387
  • 作为产物:
    描述:
    (2S,3S,4S,5R,6R,7R)-N-benzyl-4,5,6-tris(benzyloxy)-7-((benzyloxy)methyl)-2-methoxyoxepan-3-amine 在 20% Pd(OH)2/C 、 氢气 作用下, 以 甲醇氯仿 为溶剂, 反应 12.0h, 以83%的产率得到
    参考文献:
    名称:
    Access to Ring-Expanded Analogues of 2-Amino Sugars
    摘要:
    Ring-expanded 2-N-acetylamino sugar analogs Of D-glucose, D-galactose, and D-mannose have been prepared by a new synthetic route. Aspects of the highly substituted (x-amino aldehyde intermediates made them central to the approach, First, they were accessed via diastereoselective addition of a vinyl Grignard onto protected glycosyl amines. Also, the sterics of the bis-protected amine favored the formation of only one glycoside anomer. The new analogues reported here should prove useful in the development of tools to investigate the role of 2-amino sugars in biology.
    DOI:
    10.1021/ol9018387
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