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| 929008-36-6

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
929008-36-6
化学式
C16H23NO4
mdl
——
分子量
293.363
InChiKey
WYBOPDQRHIJHSG-KKUMJFAQSA-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):
    1.56
  • 重原子数:
    21.0
  • 可旋转键数:
    3.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.62
  • 拓扑面积:
    51.16
  • 氢给体数:
    1.0
  • 氢受体数:
    5.0

反应信息

  • 作为反应物:
    描述:
    在 palladium on activated charcoal 吡啶氢气potassium carbonate溶剂黄146三乙胺 作用下, 以 甲醇二氯甲烷 为溶剂, 反应 25.17h, 生成 (3S,4S,5S)-N-benzyl-3,4-diacetoxy-5-(acetoxymethyl)piperidine
    参考文献:
    名称:
    Synthesis of (−)‐Isofagomine
    摘要:
    1,3-Dipolar cycloaddition of N-benzyl nitrone 2 to delta-lactone 15 proceeded with excellent stereoselectivity to provide only one adduct 16. Cycloadduct 16 was subsequently subjected to a sequence of reactions involving rearrangement to gamma-lactone, glycolic cleavage/reduction, protection of the terminal hydroxymethyl group, reduction of the lactone, desilylation/mesylation, and hydrogenolysis of the N-O bond providing (-)-isofagomine and its N-substituted derivatives. The biologic activity of N-substituted (-)-isofagomines toward commercially available alpha- and beta-glucosidases, alpha-D-mannosidase, alpha-L-fucosidase, beta-D-glucuronidase, and beta-D-galactosidase was tested.
    DOI:
    10.1080/07328300601039336
  • 作为产物:
    参考文献:
    名称:
    Synthesis of (−)‐Isofagomine
    摘要:
    1,3-Dipolar cycloaddition of N-benzyl nitrone 2 to delta-lactone 15 proceeded with excellent stereoselectivity to provide only one adduct 16. Cycloadduct 16 was subsequently subjected to a sequence of reactions involving rearrangement to gamma-lactone, glycolic cleavage/reduction, protection of the terminal hydroxymethyl group, reduction of the lactone, desilylation/mesylation, and hydrogenolysis of the N-O bond providing (-)-isofagomine and its N-substituted derivatives. The biologic activity of N-substituted (-)-isofagomines toward commercially available alpha- and beta-glucosidases, alpha-D-mannosidase, alpha-L-fucosidase, beta-D-glucuronidase, and beta-D-galactosidase was tested.
    DOI:
    10.1080/07328300601039336
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