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Acetic acid (2R,3R,4R,5R,6S)-3,5-diacetoxy-2-hydroxymethyl-6-methyl-tetrahydro-pyran-4-yl ester | 145933-71-7

中文名称
——
中文别名
——
英文名称
Acetic acid (2R,3R,4R,5R,6S)-3,5-diacetoxy-2-hydroxymethyl-6-methyl-tetrahydro-pyran-4-yl ester
英文别名
[(2S,3R,4R,5R,6R)-4,5-diacetyloxy-6-(hydroxymethyl)-2-methyloxan-3-yl] acetate
Acetic acid (2R,3R,4R,5R,6S)-3,5-diacetoxy-2-hydroxymethyl-6-methyl-tetrahydro-pyran-4-yl ester化学式
CAS
145933-71-7
化学式
C13H20O8
mdl
——
分子量
304.297
InChiKey
AWLQFSNENKZMPF-WSBJEXOASA-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):
    -0.5
  • 重原子数:
    21
  • 可旋转键数:
    7
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.77
  • 拓扑面积:
    108
  • 氢给体数:
    1
  • 氢受体数:
    8

反应信息

  • 作为反应物:
    描述:
    Acetic acid (2R,3R,4R,5R,6S)-3,5-diacetoxy-2-hydroxymethyl-6-methyl-tetrahydro-pyran-4-yl esterplatinum(IV) oxide 吡啶氢气 作用下, 以 甲醇 为溶剂, 25.0 ℃ 、101.33 kPa 条件下, 反应 50.0h, 生成 Acetic acid (2S,3R,4R,5R,6R)-3,5-diacetoxy-2-methyl-6-phosphonooxymethyl-tetrahydro-pyran-4-yl ester
    参考文献:
    名称:
    Synthesis of C-fucopyranosyl analogs of GDP-L-fucose as inhibitors of fucosyltransferases
    摘要:
    The syntheses of the C-fucopyranosyl analogs of GDP-L-fucose 2 - 5 as potential inhibitors of fucosyltransferases are reported. The synthetic routes are based on the C-glycosidation of tetra-O-acetyl-alpha-L-fucopyranose 6 under conditions that provided either beta- or alpha- C-fucosides with high stereoselectivity. Coupling to GMP was effected by Khorana's phosphomorpholidate method.
    DOI:
    10.1016/s0040-4039(00)60893-6
  • 作为产物:
    描述:
    Acetic acid (2R,3R,4R,5R,6S)-4,5-diacetoxy-2-(diethyl-methyl-silanyloxymethyl)-6-methyl-tetrahydro-pyran-3-yl ester溶剂黄146 作用下, 以 四氢呋喃 为溶剂, 以98%的产率得到Acetic acid (2R,3R,4R,5R,6S)-3,5-diacetoxy-2-hydroxymethyl-6-methyl-tetrahydro-pyran-4-yl ester
    参考文献:
    名称:
    Synthesis of C-fucopyranosyl analogs of GDP-L-fucose as inhibitors of fucosyltransferases
    摘要:
    The syntheses of the C-fucopyranosyl analogs of GDP-L-fucose 2 - 5 as potential inhibitors of fucosyltransferases are reported. The synthetic routes are based on the C-glycosidation of tetra-O-acetyl-alpha-L-fucopyranose 6 under conditions that provided either beta- or alpha- C-fucosides with high stereoselectivity. Coupling to GMP was effected by Khorana's phosphomorpholidate method.
    DOI:
    10.1016/s0040-4039(00)60893-6
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