(1R)-7-azido-3,4,5,8-tetra-O-benzyl-2,7,9-trideoxy-1-C-heptyl-2-nitro-D-erythro-α-D-galacto-non-2-ulopyranose | 1146962-82-4

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: (1R)-7-azido-3,4,5,8-tetra-O-benzyl-2,7,9-trideoxy-1-C-heptyl-2-nitro-D-erythro-α-D-galacto-non-2-ulopyranose
• CAS: 1146962-82-4
• 化学式: C₄₄H₅₄N₄O₈
• 分子量: 766.935
• InChiKey: XWNKZFWQYOQKEH-FWOBLYFFSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  9.12
• 重原子数：
  56.0
• 可旋转键数：
  23.0
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.45
• 拓扑面积：
  158.28
• 氢给体数：
  1.0
• 氢受体数：
  9.0

反应信息

• 作为反应物：
  描述：

  (1R)-7-azido-3,4,5,8-tetra-O-benzyl-2,7,9-trideoxy-1-C-heptyl-2-nitro-D-erythro-α-D-galacto-non-2-ulopyranose 在 盐酸 作用下， 以 水 为溶剂， 反应 36.0h， 生成
  参考文献：
  名称：

  林可霉素的S和C（1）取代类似物的合成和评价

  摘要：

  Abstractmagnified imageNew thioglycosides and C(1)‐alkylated thioglycosides (S‐ulosides) of lincomycin were synthesized, and their antibiotic activities were determined. The S‐aryl and S‐arylalkyl analogues 11a–11i were obtained by S‐glycosylation of the sulfoxides 7 with arenethiols, or by S‐alkylation of the thiol 14 with alkyl bromides. Lincomycin derivatives 27, 32a, 32b, 38a, 38b, 44, and 47 were prepared via Henry reaction or Michael addition of the lincosamine‐derived 1‐deoxy‐1‐nitropyranoses 22. The S‐alkyl derivatives showed a similar activity and specificity as lincomycin. Lipophilic S‐uloside analogues were two‐ to fourfold less active than the parent antibiotic, whilst the hydrophilic analogues were inactive.

  DOI：

  10.1002/hlca.200800343
• 作为产物：
  描述：

  正辛醛 、 6-azido-2,3,4,7-tetra-O-benzyl-1,6,8-trideoxy-1-nitro-D-erythro-D-galacto-octopyranose 在 四乙基氢氧化铵 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 24.0h， 以53%的产率得到(1R)-7-azido-3,4,5,8-tetra-O-benzyl-2,7,9-trideoxy-1-C-heptyl-2-nitro-D-erythro-α-D-galacto-non-2-ulopyranose
  参考文献：
  名称：

  林可霉素的S和C（1）取代类似物的合成和评价

  摘要：

  Abstractmagnified imageNew thioglycosides and C(1)‐alkylated thioglycosides (S‐ulosides) of lincomycin were synthesized, and their antibiotic activities were determined. The S‐aryl and S‐arylalkyl analogues 11a–11i were obtained by S‐glycosylation of the sulfoxides 7 with arenethiols, or by S‐alkylation of the thiol 14 with alkyl bromides. Lincomycin derivatives 27, 32a, 32b, 38a, 38b, 44, and 47 were prepared via Henry reaction or Michael addition of the lincosamine‐derived 1‐deoxy‐1‐nitropyranoses 22. The S‐alkyl derivatives showed a similar activity and specificity as lincomycin. Lipophilic S‐uloside analogues were two‐ to fourfold less active than the parent antibiotic, whilst the hydrophilic analogues were inactive.

  DOI：

  10.1002/hlca.200800343