4-methoxyphenyl (methyl 5-acetamido-4,7,8,9-tetra-O-acetyl-3,5-dideoxy-2-thio-D-glycero-α-D-galacto-2-nonulopyranosid) onate | 144988-65-8

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: 4-methoxyphenyl (methyl 5-acetamido-4,7,8,9-tetra-O-acetyl-3,5-dideoxy-2-thio-D-glycero-α-D-galacto-2-nonulopyranosid) onate
• 英文别名: methyl (2S,4S,5R,6R)-5-acetamido-4-acetyloxy-2-(4-methoxyphenyl)sulfanyl-6-[(1S,2R)-1,2,3-triacetyloxypropyl]oxane-2-carboxylate
• CAS: 144988-65-8
• 化学式: C₂₇H₃₅NO₁₃S
• 分子量: 613.64
• InChiKey: WCRWVYLOZALXJK-NFIQMXJASA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.5
• 重原子数：
  42
• 可旋转键数：
  17
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.56
• 拓扑面积：
  204
• 氢给体数：
  1
• 氢受体数：
  14

反应信息

• 作为反应物：
  描述：

  4-methoxyphenyl (methyl 5-acetamido-4,7,8,9-tetra-O-acetyl-3,5-dideoxy-2-thio-D-glycero-α-D-galacto-2-nonulopyranosid) onate 、 双丙酮半乳糖 在 N-iodosuccinimine-triflic acid 作用下， 以 二氯甲烷 、 乙腈 为溶剂， 反应 2.0h， 以89%的产率得到Neu5Ac(2-6)Gal
  参考文献：
  名称：

  “Active” and “latent” thioglycosyl donors in oligosaccharide synthesis. Application to the synthesis of α-sialosides

  摘要：

  The use of a new "active" and "latent" thioglycosyl donor strategy in glycoside synthesis is described using arylthio alpha-sialosides of different reactivities.

  DOI：

  10.1016/s0040-4039(00)60004-7
• 作为产物：
  描述：

  4-甲氧基苯硫酚 、 N-acetyl-4,7,8,9-tetra-O-acetyl-2-chloro-2-deoxyneuraminic acid methyl ester 在 四丁基硫酸氢铵 、 sodium carbonate 作用下， 以 乙酸乙酯 为溶剂， 反应 1.0h， 以81%的产率得到4-methoxyphenyl (methyl 5-acetamido-4,7,8,9-tetra-O-acetyl-3,5-dideoxy-2-thio-D-glycero-α-D-galacto-2-nonulopyranosid) onate
  参考文献：
  名称：

  Mild stereoselective syntheses of thioglycosides under PTC conditions and their use as active and latent glycosyl donors

  摘要：

  Mild and stereoselective arylthio glycoside syntheses were accomplished by inversion of configuration of glycosyl halides under phase transfer catalyzed conditions. Under such conditions, aryl alpha-thiosialosides having electron donating and withdrawing substituents were evaluated as active and latent thioglycosyl donors. A sialyl-alpha-(2-->6)-galactoside was prepared in good yield using the above strategy.

  DOI：

  10.1016/s0957-4166(00)86308-9