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[(2R,3S,4R,5R,6R)-5-acetamido-3,4-diacetyloxy-6-[4-(dodecoxymethyl)triazol-1-yl]oxan-2-yl]methyl acetate | 1083009-03-3

中文名称
——
中文别名
——
英文名称
[(2R,3S,4R,5R,6R)-5-acetamido-3,4-diacetyloxy-6-[4-(dodecoxymethyl)triazol-1-yl]oxan-2-yl]methyl acetate
英文别名
——
[(2R,3S,4R,5R,6R)-5-acetamido-3,4-diacetyloxy-6-[4-(dodecoxymethyl)triazol-1-yl]oxan-2-yl]methyl acetate化学式
CAS
1083009-03-3
化学式
C29H48N4O9
mdl
——
分子量
596.722
InChiKey
JRTZILWDARPNJL-HWVUQVAQSA-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):
    3.9
  • 重原子数:
    42
  • 可旋转键数:
    22
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.79
  • 拓扑面积:
    157
  • 氢给体数:
    1
  • 氢受体数:
    11

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Synthesis of novel glycolipids derived from glycopyranosyl azides and N-(β-glycopyranosyl)azidoacetamides
    摘要:
    A general and expedient method based on a click reaction has been developed for the synthesis of novel glycolipids. The Cu(I) catalyzed [3+2] cycloaddition of several fully acetylated beta- as well as alpha-D-glycopyranosyl azides, including the 1,6-diazide derived from D-glucose, with long chain alkyl propargyl ethers gave the respective 1,4-substituted 1,2,3-triazole derivatives in good yields. Treatment of fully acetylated N-(beta-glycopyranosyl)azidoacetamides under similar conditions with alkyl propargyl ethers afforded the 1,2,3-triazolylacetamido derivatives in fairly good yields. Zemplen de-O-acetylation of all the fully acetylated derivatives furnished the free glycolipids in quantitative yields. (c) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2008.08.073
  • 作为产物:
    描述:
    n-dodecyl propargyl ether2-乙酰氨基-3,4,6-三-O-乙酰基-2-脱氧-Β-D-吡喃葡萄糖酰基叠氮化物 在 copper diacetate 、 sodium ascorbate 作用下, 以 丙酮 为溶剂, 以73%的产率得到[(2R,3S,4R,5R,6R)-5-acetamido-3,4-diacetyloxy-6-[4-(dodecoxymethyl)triazol-1-yl]oxan-2-yl]methyl acetate
    参考文献:
    名称:
    Synthesis of novel glycolipids derived from glycopyranosyl azides and N-(β-glycopyranosyl)azidoacetamides
    摘要:
    A general and expedient method based on a click reaction has been developed for the synthesis of novel glycolipids. The Cu(I) catalyzed [3+2] cycloaddition of several fully acetylated beta- as well as alpha-D-glycopyranosyl azides, including the 1,6-diazide derived from D-glucose, with long chain alkyl propargyl ethers gave the respective 1,4-substituted 1,2,3-triazole derivatives in good yields. Treatment of fully acetylated N-(beta-glycopyranosyl)azidoacetamides under similar conditions with alkyl propargyl ethers afforded the 1,2,3-triazolylacetamido derivatives in fairly good yields. Zemplen de-O-acetylation of all the fully acetylated derivatives furnished the free glycolipids in quantitative yields. (c) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2008.08.073
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