2-(4-methoxyphenoxy)ethyl (2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)-(1->6)-2-O-allyl-3,4-di-O-benzyl-β-D-glucopyranoside | 1215022-01-7

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 2-(4-methoxyphenoxy)ethyl (2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)-(1->6)-2-O-allyl-3,4-di-O-benzyl-β-D-glucopyranoside
• CAS: 1215022-01-7
• 化学式: C₆₆H₇₂O₁₃
• 分子量: 1073.29
• InChiKey: DTOFVHOCASKTMR-XAZZOBJXSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  11.27
• 重原子数：
  79.0
• 可旋转键数：
  31.0
• 环数：
  9.0
• sp3杂化的碳原子比例：
  0.33
• 拓扑面积：
  119.99
• 氢给体数：
  0.0
• 氢受体数：
  13.0

反应信息

• 作为反应物：
  描述：

  2-(4-methoxyphenoxy)ethyl (2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)-(1->6)-2-O-allyl-3,4-di-O-benzyl-β-D-glucopyranoside 在 甲醇 、 palladium dichloride 作用下， 反应 2.0h， 以78%的产率得到2-(4-methoxyphenoxy)ethyl (2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)-(1->6)-3,4-di-O-benzyl-β-D-glucopyranoside
  参考文献：
  名称：

  Synthesis of a tetrasaccharide corresponding to the teichoic acid from the cell wall of Streptomyces sp. VKM Ac-2275

  摘要：

  A concise chemical synthesis of a tetrasaccharide found in the teichoic acid from the cell wall of Streptomyces sp. VKM Ac-2275 was achieved in high yield. A [2+2] block synthetic strategy has been adopted for the construction of the target tetrasaccharide by exploiting the orthogonal property of a thioglycoside. For the first time, the 2-(4-methoxyphenoxy) ethyl group has been used as the anomeric protecting group to make the glycone moiety with a readily available linker for its conjugation to a protein without destroying the cyclic structure at the reducing end. Yields were high in all of the intermediate steps. (C) 2009 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetasy.2009.10.035
• 作为产物：
  描述：

  2-(4-methoxyphenoxy)ethyl (2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-(1->6)-2-O-allyl-3,4-di-O-benzyl-β-D-glucopyranoside 、 溴甲苯 在 四丁基溴化铵 、 sodium hydroxide 作用下， 以 四氢呋喃 为溶剂， 反应 4.0h， 以86%的产率得到2-(4-methoxyphenoxy)ethyl (2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)-(1->6)-2-O-allyl-3,4-di-O-benzyl-β-D-glucopyranoside
  参考文献：
  名称：

  Synthesis of a tetrasaccharide corresponding to the teichoic acid from the cell wall of Streptomyces sp. VKM Ac-2275

  摘要：

  A concise chemical synthesis of a tetrasaccharide found in the teichoic acid from the cell wall of Streptomyces sp. VKM Ac-2275 was achieved in high yield. A [2+2] block synthetic strategy has been adopted for the construction of the target tetrasaccharide by exploiting the orthogonal property of a thioglycoside. For the first time, the 2-(4-methoxyphenoxy) ethyl group has been used as the anomeric protecting group to make the glycone moiety with a readily available linker for its conjugation to a protein without destroying the cyclic structure at the reducing end. Yields were high in all of the intermediate steps. (C) 2009 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetasy.2009.10.035