thexyldimethylsilyl 2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl-(1->4)-6-O-acetyl-2-azido-2-deoxy-β-D-glucopyranoside | 320351-55-1

• 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: thexyldimethylsilyl 2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl-(1->4)-6-O-acetyl-2-azido-2-deoxy-β-D-glucopyranoside
• CAS: 320351-55-1
• 化学式: C₃₀H₄₉N₃O₁₅Si
• 分子量: 719.816
• InChiKey: JCBNXIXOIXEZDS-VSIMVOGDSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.44
• 重原子数：
  49.0
• 可旋转键数：
  14.0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.83
• 拓扑面积：
  237.41
• 氢给体数：
  1.0
• 氢受体数：
  16.0

反应信息

• 作为反应物：
  描述：

  3,4-di-O-acetyl-2-O-benzyl-α-L-fucopyranosyl trichloroacetimidate 、 thexyldimethylsilyl 2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl-(1->4)-6-O-acetyl-2-azido-2-deoxy-β-D-glucopyranoside 在 三氟甲磺酸三甲基硅酯 作用下， 以 二氯甲烷 为溶剂， 反应 0.5h， 以90%的产率得到thexyldimethylsilyl 2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl-(1->4)-[3,4-di-O-acetyl-2-O-benzyl-α-L-fucopyranosyl-(1->3)]-6-O-acetyl-2-azido-2-deoxy-β-D-glucopyranoside
  参考文献：
  名称：

  Synthesis of building blocks of human milk oligosaccharides. Fucosylated derivatives of the lacto- and neolacto-series

  摘要：

  The synthesis of protected fucosylated derivatives of a Gal beta(1--> 3)GlcNAc and of lactosamine Galbeta(1--> 4)GlcNAc building blocks contained in human milk oligosaccharides is described. Both chemical and enzymatic methods have been exploited for selective protection of the disaccharide. Fucosylation of the appropriate derivatives allowed an easy and relatively short access to different products from common precursors. (C) 2002 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0008-6215(02)00164-7
• 作为产物：
  描述：

  dimethylthexylsilyl 6-O-acetyl-2-azido-3-O-benzyl-2-deoxy-β-D-glucopyranoside 在 三氟甲磺酸三甲基硅酯 、 四氯化锡 作用下， 以 二氯甲烷 为溶剂， 反应 39.0h， 生成 thexyldimethylsilyl 2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl-(1->4)-6-O-acetyl-2-azido-2-deoxy-β-D-glucopyranoside
  参考文献：
  名称：

  Synthesis of building blocks of human milk oligosaccharides. Fucosylated derivatives of the lacto- and neolacto-series

  摘要：

  The synthesis of protected fucosylated derivatives of a Gal beta(1--> 3)GlcNAc and of lactosamine Galbeta(1--> 4)GlcNAc building blocks contained in human milk oligosaccharides is described. Both chemical and enzymatic methods have been exploited for selective protection of the disaccharide. Fucosylation of the appropriate derivatives allowed an easy and relatively short access to different products from common precursors. (C) 2002 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0008-6215(02)00164-7