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1-<5-O-(p-chlorobenzoyl)-β-D-glycero-pentafuranosyl>uracil | 132575-56-5

中文名称
——
中文别名
——
英文名称
1-<5-O-(p-chlorobenzoyl)-β-D-glycero-pentafuranosyl>uracil
英文别名
[(2S,5R)-5-(2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methyl 4-chlorobenzoate
1-<5-O-(p-chlorobenzoyl)-β-D-glycero-pentafuranosyl>uracil化学式
CAS
132575-56-5;132619-99-9
化学式
C16H15ClN2O5
mdl
——
分子量
350.759
InChiKey
IWRSLJSKSOIVAV-GXTWGEPZSA-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):
    2
  • 重原子数:
    24
  • 可旋转键数:
    5
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.31
  • 拓扑面积:
    84.9
  • 氢给体数:
    1
  • 氢受体数:
    5

反应信息

  • 作为产物:
    描述:
    4-Chloro-benzoic acid (S)-5-oxo-tetrahydro-furan-2-ylmethyl ester 在 吡啶盐酸二异丁基氢化铝 、 magnesium sulfate 作用下, 以 四氢呋喃氯仿甲苯 为溶剂, 反应 6.0h, 生成 1-<5-O-(p-chlorobenzoyl)-β-D-glycero-pentafuranosyl>uracil
    参考文献:
    名称:
    Stereoselectivities in the Coupling Reaction between Silylated Pyrimidine Bases and 1-Halo-2,3-dideoxyribose
    摘要:
    Coupling reactions between 1-chloro-2,3-dideoxyribose and silylated pyrimidines have been examined from the point of stereoselectivity. When the reaction was carried out in chloroform, the selectivity was in the anomeric ratio of alpha:beta = 4:6. On the other hand, the presence of tertiary amine raises the selectivity to alpha:beta = 3:7.
    DOI:
    10.3987/com-90-5563
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文献信息

  • KAWAKAMI, HIROSHI;EBATA, TAKASHI;KOSEKI, KOSHI;MATSUMOTO, KATSUYA;MATSUSH+, HETEROCYCLES, 31,(1990) N1, C. 2041-2054
    作者:KAWAKAMI, HIROSHI、EBATA, TAKASHI、KOSEKI, KOSHI、MATSUMOTO, KATSUYA、MATSUSH+
    DOI:——
    日期:——
  • Stereoselectivities in the Coupling Reaction between Silylated Pyrimidine Bases and 1-Halo-2,3-dideoxyribose
    作者:Hiroshi Kawakami、Takashi Ebata、Koshi Koseki、Katsuya Matsumoto、Hajime Matsushita、Yoshitake Naoi、Kazuo Itoh
    DOI:10.3987/com-90-5563
    日期:——
    Coupling reactions between 1-chloro-2,3-dideoxyribose and silylated pyrimidines have been examined from the point of stereoselectivity. When the reaction was carried out in chloroform, the selectivity was in the anomeric ratio of alpha:beta = 4:6. On the other hand, the presence of tertiary amine raises the selectivity to alpha:beta = 3:7.
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