2,3,5,6-tetra-O-acetyl-β-D-galactofuranosyl-(1-3)-2-O-benzyl-4,6-O-DTBS-α-D-galactopyranosyl fluoride | 1196690-78-4

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 2,3,5,6-tetra-O-acetyl-β-D-galactofuranosyl-(1-3)-2-O-benzyl-4,6-O-DTBS-α-D-galactopyranosyl fluoride
• CAS: 1196690-78-4
• 化学式: C₃₅H₅₁FO₁₄Si
• 分子量: 742.865
• InChiKey: SXUUCOOFUXGNHX-PXFBUNEYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.19
• 重原子数：
  51.0
• 可旋转键数：
  11.0
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.71
• 拓扑面积：
  160.58
• 氢给体数：
  0.0
• 氢受体数：
  14.0

反应信息

• 作为产物：
  描述：

  2,3,5,6-tetra-O-acetyl-β-D-galactofuranosyl-(1-3)-2-O-benzyl-4,6-O-DTBS-D-galactopyranoside 在 二乙胺基三氟化硫 作用下， 以 二氯甲烷 为溶剂， 反应 2.0h， 以49%的产率得到2,3,5,6-tetra-O-acetyl-β-D-galactofuranosyl-(1-3)-2-O-benzyl-4,6-O-DTBS-α-D-galactopyranosyl fluoride
  参考文献：
  名称：

  Synthesis of the starfish ganglioside AG2 pentasaccharide

  摘要：

  This Letter reports the first synthesis of the AG2 pentasaccharide, using silylene-oxazolidinone double-locked sialic acid building blocks. The di-DTBS-protected sialic acid building block was easily prepared and readily activated with NIS and TfOH to provide the sialylated lactose unit in good yield with moderate selectivity. After obtaining the trisaccharide unit, the oxazolidinone-protected C4-OH on the sialic acid residue was readily deprotected by treatment with NaOMe. Coupling with the galactofuranosyl beta(1-3)galactopyranosyl fluoride building block produced the desired AG2 pentasaccharide in a highly stereoselective manner. Finally, the desired AG2 pentasaccharide was obtained in good yield following global deprotection. (C) 2009 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2009.08.071