methyl (methyl 3-O-benzyl-2-deoxy-2-phthalimido-α-D-altropyranosid)uronate

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: methyl (methyl 3-O-benzyl-2-deoxy-2-phthalimido-α-D-altropyranosid)uronate
• 英文别名: methyl (2S,3S,4S,5S,6S)-5-(1,3-dioxoisoindol-2-yl)-3-hydroxy-6-methoxy-4-phenylmethoxyoxane-2-carboxylate
• 化学式: C₂₃H₂₃NO₈
• 分子量: 441.438
• InChiKey: ZYOBJORHLDGOMV-QUVRYOLLSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.9
• 重原子数：
  32
• 可旋转键数：
  7
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.35
• 拓扑面积：
  112
• 氢给体数：
  1
• 氢受体数：
  8

反应信息

• 作为产物：
  描述：

  methyl 2-azido-3-O-benzyl-2-deoxy-α-D-altropyranoside 在 palladium on activated charcoal 2,2,6,6-tetramethyl-piperidine-N-oxyl 、 sodium hypochlorite 、 氢气 、 碳酸氢钠 、 三乙胺 作用下， 以 吡啶 、 甲醇 、 二氯甲烷 、 水 、 N,N-二甲基甲酰胺 为溶剂， 反应 26.0h， 生成 methyl (methyl 3-O-benzyl-2-deoxy-2-phthalimido-α-D-altropyranosid)uronate
  参考文献：
  名称：

  Synthetic Studies Towards theO-Specific Polysaccharide ofShigella Sonnei

  摘要：

  Synthetic routes are described to zwitter-ionic disaccharides that are diastereoisomerically related to frame-shifted repeating units of the title polysaccharide that contains 2-acetamido-4-amino-2,4,6-trideoxy-D-galactose and 2-acetamido-2-deoxy-L-altruronic acid. The intermediates corresponding to the trideoxygalactose residue feature acylamino functions at C-2 and an azido group at C-4. Best results were obtained with N-phthaloyl- and N-trichloroacetyl-protected derivatives. The intermediates corresponding to the uronic acid residue were either a D-altruronic acid-derived acceptor or a D-altrose-derived donor in which C-6 was oxidized after disaccharide formation.

  DOI：

  10.1080/07328300008544079

文献信息

• Synthetic Studies Towards the<i>O</i>-Specific Polysaccharide of<i>Shigella Sonnei</i>
  作者：Adél Medgyes、István Bajza、Erzsébet Farkas、Vince Pozsgay、András Lipták

  DOI：10.1080/07328300008544079

  日期：2000.1

  Synthetic routes are described to zwitter-ionic disaccharides that are diastereoisomerically related to frame-shifted repeating units of the title polysaccharide that contains 2-acetamido-4-amino-2,4,6-trideoxy-D-galactose and 2-acetamido-2-deoxy-L-altruronic acid. The intermediates corresponding to the trideoxygalactose residue feature acylamino functions at C-2 and an azido group at C-4. Best results were obtained with N-phthaloyl- and N-trichloroacetyl-protected derivatives. The intermediates corresponding to the uronic acid residue were either a D-altruronic acid-derived acceptor or a D-altrose-derived donor in which C-6 was oxidized after disaccharide formation.