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3-acetamido-2,6-anhydro-4,5,7-tri-O-benzyl-1,3-dideoxy-1-dimethoxyphosphoryl-D-glycero-L-manno-heptitol | 271243-86-8

中文名称
——
中文别名
——
英文名称
3-acetamido-2,6-anhydro-4,5,7-tri-O-benzyl-1,3-dideoxy-1-dimethoxyphosphoryl-D-glycero-L-manno-heptitol
英文别名
——
3-acetamido-2,6-anhydro-4,5,7-tri-O-benzyl-1,3-dideoxy-1-dimethoxyphosphoryl-D-glycero-L-manno-heptitol化学式
CAS
271243-86-8
化学式
C32H40NO8P
mdl
——
分子量
597.645
InChiKey
ZDOCCYOLJXLBNP-GCIGRYLYSA-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):
    5.13
  • 重原子数:
    42.0
  • 可旋转键数:
    15.0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.41
  • 拓扑面积:
    101.55
  • 氢给体数:
    1.0
  • 氢受体数:
    8.0

反应信息

  • 作为反应物:
    描述:
    3-acetamido-2,6-anhydro-4,5,7-tri-O-benzyl-1,3-dideoxy-1-dimethoxyphosphoryl-D-glycero-L-manno-heptitolpalladium dihydroxide 氢气 作用下, 以 甲醇乙酸乙酯 为溶剂, 反应 3.0h, 以98%的产率得到3-acetamido-2,6-anhydro-1,3-dideoxy-1-dimethoxyphosphoryl-D-glycero-L-manno-heptitol
    参考文献:
    名称:
    Stereoselective synthesis of C-glycosylphosphonates from their ketols. Reconsideration of an abandoned route
    摘要:
    Isosteric phosphonate analogues of glycosyl 1-phosphates have been obtained by addition of LiCH2P(O)(OMe)(2) to glyconolactones followed by Et3SiH-TMSOTf reductive dehydroxylation of the resultant ketols. The compounds prepared include four beta-linked pyranose derivatives (D-galacto, 2-azido-2-deoxy-D-galacto, D-gluco, D-manno) and one beta-linked furanose derivative (D-manno). In the latter case the ketol was activated as its 2-acetate. In agreement with an observation in another laboratory, the dehydroxylation of a model ketol phosphonate failed with the use of Et3SiH-BF3. Et2O. (C) 2000 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0957-4166(99)00477-2
  • 作为产物:
    参考文献:
    名称:
    Stereoselective synthesis of C-glycosylphosphonates from their ketols. Reconsideration of an abandoned route
    摘要:
    Isosteric phosphonate analogues of glycosyl 1-phosphates have been obtained by addition of LiCH2P(O)(OMe)(2) to glyconolactones followed by Et3SiH-TMSOTf reductive dehydroxylation of the resultant ketols. The compounds prepared include four beta-linked pyranose derivatives (D-galacto, 2-azido-2-deoxy-D-galacto, D-gluco, D-manno) and one beta-linked furanose derivative (D-manno). In the latter case the ketol was activated as its 2-acetate. In agreement with an observation in another laboratory, the dehydroxylation of a model ketol phosphonate failed with the use of Et3SiH-BF3. Et2O. (C) 2000 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0957-4166(99)00477-2
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