2-(4-methoxyphenoxy)ethyl 2-O-allyl-3,4-di-O-benzyl-β-D-glucopyranoside | 1215021-92-3

• 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-O-allyl-3,4-di-O-benzyl-β-D-glucopyranoside
• 英文别名: [(2R,3R,4S,5R,6R)-6-[2-(4-methoxyphenoxy)ethoxy]-3,4-bis(phenylmethoxy)-5-prop-2-enoxyoxan-2-yl]methanol
• CAS: 1215021-92-3
• 化学式: C₃₂H₃₈O₈
• 分子量: 550.649
• InChiKey: DCJCJQVLIZEIOT-HXBJCGEWSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.3
• 重原子数：
  40
• 可旋转键数：
  16
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.38
• 拓扑面积：
  84.8
• 氢给体数：
  1
• 氢受体数：
  8

反应信息

• 作为反应物：
  描述：

  2-(4-methoxyphenoxy)ethyl 2-O-allyl-3,4-di-O-benzyl-β-D-glucopyranoside 、 ethyl 2,3,4,6-tetra-O-acetyl-1-thio-β-D-glucopyranoside 在 N-碘代丁二酰亚胺 、 三氟甲磺酸 作用下， 以 二氯甲烷 为溶剂， 反应 1.0h， 以88%的产率得到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
  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-O-allyl-3-O-benzyl-4,6-O-benzylidene-β-D-glucopyranoside 在 aluminum (III) chloride 、 lithium aluminium tetrahydride 作用下， 以 乙醚 、 二氯甲烷 为溶剂， 反应 2.0h， 以76%的产率得到2-(4-methoxyphenoxy)ethyl 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

文献信息

• Synthesis of a tetrasaccharide corresponding to the teichoic acid from the cell wall of Streptomyces sp. VKM Ac-2275
  作者：Samir Ghosh、Anup Kumar Misra

  DOI：10.1016/j.tetasy.2009.10.035

  日期：2009.12

  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.