n-octyl 2,6-dideoxy-α-L-lyxo-hexopyranosyl-(1->2)-3-azido-3-deoxy-β-D-galactopyranoside | 904285-76-3

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 脂肪酰基
• 英文名称: n-octyl 2,6-dideoxy-α-L-lyxo-hexopyranosyl-(1->2)-3-azido-3-deoxy-β-D-galactopyranoside
• CAS: 904285-76-3
• 化学式: C₂₀H₃₇N₃O₈
• 分子量: 447.529
• InChiKey: KCYGPMZWBZHEMT-HTYYFBMYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.36
• 重原子数：
  31.0
• 可旋转键数：
  12.0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  166.6
• 氢给体数：
  4.0
• 氢受体数：
  9.0

反应信息

• 作为反应物：
  描述：

  n-octyl 2,6-dideoxy-α-L-lyxo-hexopyranosyl-(1->2)-3-azido-3-deoxy-β-D-galactopyranoside 在 palladium dihydroxide 氢气 作用下， 以 甲醇 为溶剂， 反应 6.0h， 以80%的产率得到n-octyl 2,6-dideoxy-α-L-lyxo-hexopyranosyl-(1->2)-3-amino-3-deoxy-β-D-galactopyranoside
  参考文献：
  名称：

  Synthesis of n-octyl 2,6-dideoxy-α-l-lyxo-hexopyranosyl-(1→2)-3-amino-3-deoxy-β-d-galactopyranoside, an analog of the H-disaccharide antigen

  摘要：

  The synthesis of an analog of the H-disaccharide antigen (2), in which the galactopyranosyl moiety bears an amino group at C-3 and the fucopyranosyl residue is deoxygenated at C-2, is reported. The key reaction in the preparation of 2 was the glycosylation of an appropriately protected n-octyl 3-azido-3-deoxy-galactopyranoside derivative with a 2,6-dideoxy thioglycoside promoted by 1-(phenylsulfinyl)piperidine and triflic anhydride. Disaccharide 2 is of interest in studies directed towards understanding the molecular basis of substrate recognition by the blood group A and B glycosyltransferases. (c) 2006 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.carres.2006.03.018
• 作为产物：
  描述：

  2,6-脱水-1,5-二脱氧-L-阿拉伯-己-5-烯糖二乙酸酯 在 三氟甲磺酸酐 ammonium cerium(IV) nitrate 、 1-(苯基亚硫酰基)哌啶 、 4 A molecular sieve 、 sodium methylate 、 2,4,6-三叔丁基嘧啶 作用下， 以 甲醇 、 二氯甲烷 、 乙腈 为溶剂， 反应 33.87h， 生成 n-octyl 2,6-dideoxy-α-L-lyxo-hexopyranosyl-(1->2)-3-azido-3-deoxy-β-D-galactopyranoside
  参考文献：
  名称：

  Synthesis of n-octyl 2,6-dideoxy-α-l-lyxo-hexopyranosyl-(1→2)-3-amino-3-deoxy-β-d-galactopyranoside, an analog of the H-disaccharide antigen

  摘要：

  The synthesis of an analog of the H-disaccharide antigen (2), in which the galactopyranosyl moiety bears an amino group at C-3 and the fucopyranosyl residue is deoxygenated at C-2, is reported. The key reaction in the preparation of 2 was the glycosylation of an appropriately protected n-octyl 3-azido-3-deoxy-galactopyranoside derivative with a 2,6-dideoxy thioglycoside promoted by 1-(phenylsulfinyl)piperidine and triflic anhydride. Disaccharide 2 is of interest in studies directed towards understanding the molecular basis of substrate recognition by the blood group A and B glycosyltransferases. (c) 2006 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.carres.2006.03.018