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6-O-acetyl-3-O-(tert-butyldimethyl)silyl-2-deoxy-2-iodo-4-O-pivaloyl-1-trichloroacetimido-α-D-glucopyranose | 245738-44-7

中文名称
——
中文别名
——
英文名称
6-O-acetyl-3-O-(tert-butyldimethyl)silyl-2-deoxy-2-iodo-4-O-pivaloyl-1-trichloroacetimido-α-D-glucopyranose
英文别名
TBDMS(-3)[pivaloyl(-4)]Glc2I6Ac(a)-O-C(NH)CCl3;[(2R,3R,4S,5R,6R)-2-(acetyloxymethyl)-4-[tert-butyl(dimethyl)silyl]oxy-5-iodo-6-(2,2,2-trichloroethanimidoyl)oxyoxan-3-yl] 2,2-dimethylpropanoate
6-O-acetyl-3-O-(tert-butyldimethyl)silyl-2-deoxy-2-iodo-4-O-pivaloyl-1-trichloroacetimido-α-D-glucopyranose化学式
CAS
245738-44-7
化学式
C21H35Cl3INO7Si
mdl
——
分子量
674.86
InChiKey
JZXAVRKKQMRITB-OXGONZEZSA-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):
    5.79
  • 重原子数:
    34
  • 可旋转键数:
    11
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.86
  • 拓扑面积:
    104
  • 氢给体数:
    1
  • 氢受体数:
    8

反应信息

  • 作为反应物:
    描述:
    甲基2,3,4-三-O-苯甲酰-α-D-吡喃葡萄糖苷6-O-acetyl-3-O-(tert-butyldimethyl)silyl-2-deoxy-2-iodo-4-O-pivaloyl-1-trichloroacetimido-α-D-glucopyranose 在 4 A molecular sieve 、 叔丁基二甲硅基三氟甲磺酸酯 作用下, 以 二氯甲烷 为溶剂, 生成 methyl 6-O-(6-O-acetyl-3-O-(tert-butyldimethyl)silyl-2-deoxy-2-iodo-4-O-pivaloyl-β-D-glucopyranosyl)-2,3,4-tri-O-benzoyl-α-D-glucopyranoside 、 methyl 6-O-(6-O-acetyl-3-O-(tert-butyldimethyl)silyl-2-deoxy-2-iodo-4-O-pivaloyl-α-D-glucopyranosyl)-2,3,4-tri-O-benzoyl-α-D-glucopyranoside
    参考文献:
    名称:
    2-Deoxy-2-iodo- and 2-Deoxy-2-bromo-α-glucopyranosyl Trichloroacetimidates:  Highly Reactive and Stereoselective Donors for the Synthesis of 2-Deoxy-β-glycosides
    摘要:
    [GRAPHICS]5-Deoxy-2-iodo- and 2-deoxy-2-bromoglucopyranosyl trichloroacetimidates 8-10 and 22 are extremely useful precursors of 2 deoxy-beta-glycosides. These reactive glycosyl donors undergo highly stereoselective glycosidation reactions at -78 degrees C with a range of glycosyl accepters using TBS-OTf as the activating agent. beta-Glycosides are obtained with greater than or equal to 19:1 selectivity in six of the seven examples reported herein.
    DOI:
    10.1021/ol9908070
  • 作为产物:
    参考文献:
    名称:
    2-Deoxy-2-iodo- and 2-Deoxy-2-bromo-α-glucopyranosyl Trichloroacetimidates:  Highly Reactive and Stereoselective Donors for the Synthesis of 2-Deoxy-β-glycosides
    摘要:
    [GRAPHICS]5-Deoxy-2-iodo- and 2-deoxy-2-bromoglucopyranosyl trichloroacetimidates 8-10 and 22 are extremely useful precursors of 2 deoxy-beta-glycosides. These reactive glycosyl donors undergo highly stereoselective glycosidation reactions at -78 degrees C with a range of glycosyl accepters using TBS-OTf as the activating agent. beta-Glycosides are obtained with greater than or equal to 19:1 selectivity in six of the seven examples reported herein.
    DOI:
    10.1021/ol9908070
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