Trifluoro-methanesulfonic acid (2S,3R,4S,6S)-4-azido-2-methyl-6-phenylsulfanyl-tetrahydro-pyran-3-yl ester | 284025-40-7

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 有机磺酸及其衍生物
• 英文名称: Trifluoro-methanesulfonic acid (2S,3R,4S,6S)-4-azido-2-methyl-6-phenylsulfanyl-tetrahydro-pyran-3-yl ester
• CAS: 284025-40-7
• 化学式: C₁₃H₁₄F₃N₃O₄S₂
• 分子量: 397.399
• InChiKey: SWOCVQLOWSVKSF-VGDYDELISA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.83
• 重原子数：
  25.0
• 可旋转键数：
  5.0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.54
• 拓扑面积：
  101.36
• 氢给体数：
  0.0
• 氢受体数：
  6.0

反应信息

• 作为反应物：
  描述：

  Trifluoro-methanesulfonic acid (2S,3R,4S,6S)-4-azido-2-methyl-6-phenylsulfanyl-tetrahydro-pyran-3-yl ester 在 lithium hydroxide 、 2,6-二叔丁基-4-甲基吡啶 、 18-冠醚-6 、 三氟甲磺酸酐 、 4 A molecular sieve 、 sodium hydride 、 氟化氢吡啶 、 三乙胺 、 间氯过氧苯甲酸 作用下， 以 四氢呋喃 、 甲醇 、 乙醚 、 二氯甲烷 、 N,N-二甲基甲酰胺 、 甲苯 为溶剂， 反应 6.24h， 生成
  参考文献：
  名称：

  Design of an Oligosaccharide Scaffold That Binds in the Minor Groove of DNA

  摘要：

  Many biological recognition events involve extensive interactions between macromolecules. Strategies to design compounds that mimic large peptides or other elements of secondary structure could be useful for blocking interactions between large surfaces. In this paper, the use of oligosaccharides as scaffolds for the design of peptidomimetics is addressed. A functionalized oligosaccharide modeled after a basic region peptide helix has been designed and synthesized. This oligosaccharide binds to duplex DNA with micromolar affinity. The mode of binding has been established by 2D NMR, and shows that the oligosaccharide binds DNA in the minor groove with one surface of the oligosaccharide contacting the floor of the DNA.

  DOI：

  10.1021/ja992513f
• 作为产物：
  描述：

  1,4-di-O-acetyl-3-azido-2,3,6-trideoxy-L-arabino-hexopyranose 在 吡啶 、 三氟化硼乙醚 、 potassium carbonate 作用下， 以 甲醇 、 二氯甲烷 为溶剂， 反应 3.33h， 生成 Trifluoro-methanesulfonic acid (2S,3R,4S,6S)-4-azido-2-methyl-6-phenylsulfanyl-tetrahydro-pyran-3-yl ester
  参考文献：
  名称：

  Design of an Oligosaccharide Scaffold That Binds in the Minor Groove of DNA

  摘要：

  Many biological recognition events involve extensive interactions between macromolecules. Strategies to design compounds that mimic large peptides or other elements of secondary structure could be useful for blocking interactions between large surfaces. In this paper, the use of oligosaccharides as scaffolds for the design of peptidomimetics is addressed. A functionalized oligosaccharide modeled after a basic region peptide helix has been designed and synthesized. This oligosaccharide binds to duplex DNA with micromolar affinity. The mode of binding has been established by 2D NMR, and shows that the oligosaccharide binds DNA in the minor groove with one surface of the oligosaccharide contacting the floor of the DNA.

  DOI：

  10.1021/ja992513f