摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

[(2R,3S,6S)-6-ethoxy-3-methoxycarbonyloxy-3,6-dihydro-2H-pyran-2-yl]methyl methyl carbonate | 162934-15-8

中文名称
——
中文别名
——
英文名称
[(2R,3S,6S)-6-ethoxy-3-methoxycarbonyloxy-3,6-dihydro-2H-pyran-2-yl]methyl methyl carbonate
英文别名
——
[(2R,3S,6S)-6-ethoxy-3-methoxycarbonyloxy-3,6-dihydro-2H-pyran-2-yl]methyl methyl carbonate化学式
CAS
162934-15-8
化学式
C12H18O8
mdl
——
分子量
290.27
InChiKey
ZHPFCBWBTKGIAK-AEJSXWLSSA-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):
    1.3
  • 重原子数:
    20
  • 可旋转键数:
    9
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.67
  • 拓扑面积:
    89.5
  • 氢给体数:
    0
  • 氢受体数:
    8

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Stereoselective Palladium(0)-Mediated Synthesis of Unsaturated 1,4-Disaccharides
    摘要:
    Unsaturated 1,4-disaccharides are obtained in quite good yields by alkylation of ethyl alpha-O-Delta(2)-glycosides, having a leaving group at C-4, with various 1-hydroxycarbohydrates in the presence of a catalytic amount of palladium(0). The reaction is regio- and stereospecific for alpha-erythro enosides 3 and 5, and only stereospecific in the case of the beta-threo enoside 7, alkylation occurring at C-4 and C-2 in this case.
    DOI:
    10.1080/07328309708006546
  • 作为产物:
    描述:
    ethyl 4,6-di-O-acetyl-2,3-dideoxy-α-D-erythrohex-2-enopyranoside 在 吡啶sodium methylate 作用下, 以 甲醇二氯甲烷 为溶剂, 反应 7.0h, 生成 [(2R,3S,6S)-6-ethoxy-3-methoxycarbonyloxy-3,6-dihydro-2H-pyran-2-yl]methyl methyl carbonate
    参考文献:
    名称:
    Stereoselective Palladium(0)-Mediated Synthesis of Unsaturated 1,4-Disaccharides
    摘要:
    Unsaturated 1,4-disaccharides are obtained in quite good yields by alkylation of ethyl alpha-O-Delta(2)-glycosides, having a leaving group at C-4, with various 1-hydroxycarbohydrates in the presence of a catalytic amount of palladium(0). The reaction is regio- and stereospecific for alpha-erythro enosides 3 and 5, and only stereospecific in the case of the beta-threo enoside 7, alkylation occurring at C-4 and C-2 in this case.
    DOI:
    10.1080/07328309708006546
点击查看最新优质反应信息

文献信息

  • Stereoselective palladium(0)-mediated synthesis of 1,4-disaccharides
    作者:Denis Sinou、Isabelle Frappa、Paul Lhoste、Stanislaw Porwanski、Boguslaw Kryczka
    DOI:10.1016/0040-4039(94)02480-y
    日期:1995.2
    Unsaturated 1,4-disaccharides are obtained in fairly good yields by alkylation of ethyl alpha-O-Delta(2)-glycosides which have a leaving group at the position 4 with various carbohg drates havillg a free anomeric hydroxyl group in the presence of a catalytic amount of palladium(0).
  • Stereoselective Palladium(0)-Mediated Synthesis of Unsaturated 1,4-Disaccharides
    作者:Isabelle Frappa、Boguslaw Kryczka、Paul Lhoste、Stanislaw Porwanski、Denis Sinou
    DOI:10.1080/07328309708006546
    日期:1997.8.1
    Unsaturated 1,4-disaccharides are obtained in quite good yields by alkylation of ethyl alpha-O-Delta(2)-glycosides, having a leaving group at C-4, with various 1-hydroxycarbohydrates in the presence of a catalytic amount of palladium(0). The reaction is regio- and stereospecific for alpha-erythro enosides 3 and 5, and only stereospecific in the case of the beta-threo enoside 7, alkylation occurring at C-4 and C-2 in this case.
查看更多