dimethyl 3-(2-(2-(2-methoxyethoxy)ethoxy)ethoxy)phenylphosphonite | 1337529-84-6

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚醚
• 英文名称: dimethyl 3-(2-(2-(2-methoxyethoxy)ethoxy)ethoxy)phenylphosphonite
• 英文别名: Dimethoxy-[3-[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]phenyl]phosphane；dimethoxy-[3-[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]phenyl]phosphane
• CAS: 1337529-84-6
• 化学式: C₁₅H₂₅O₆P
• 分子量: 332.334
• InChiKey: GJTSAWAOHNICDY-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.7
• 重原子数：
  22
• 可旋转键数：
  13
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.6
• 拓扑面积：
  55.4
• 氢给体数：
  0
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  dimethyl 3-(2-(2-(2-methoxyethoxy)ethoxy)ethoxy)phenylphosphonite 在 dimethyl sulfide borane 作用下， 以 乙醚 为溶剂， 反应 15.0h， 以3.6958 g的产率得到dimethyl-3-(2-(2-(2-methoxyethoxy)ethoxy)ethoxy)phenylphosphoniteborane
  参考文献：
  名称：

  Staudinger-Phosphonite Reactions for the Chemoselective Transformation of Azido-Containing Peptides and Proteins

  摘要：

  Site-specific functionalization of proteins by bloorthogonal modification offers a convenient pathway to create, modify, and study biologically active biopolymers. In this paper the Staudinger reaction of aryl-phosphonites for the chemoselective functionalization of azido-peptides and proteins was probed. Different water-soluble phosphonites with ollgoethylene substituents were synthesized and reacted with unprotected azido-containing peptides in aqueous systems at room temperature in high conversions. Finally, the Staudinger-phosphonite reaction was successfully applied to the site-specific modification of the protein calmodulin.

  DOI：

  10.1021/ol2020175
• 作为产物：
  描述：

  三甘醇单甲醚 在 正丁基锂 、 三甲胺盐酸盐 、 potassium carbonate 、 三乙胺 作用下， 以 乙醚 、 乙腈 为溶剂， 反应 24.5h， 生成 dimethyl 3-(2-(2-(2-methoxyethoxy)ethoxy)ethoxy)phenylphosphonite
  参考文献：
  名称：

  Staudinger-Phosphonite Reactions for the Chemoselective Transformation of Azido-Containing Peptides and Proteins

  摘要：

  Site-specific functionalization of proteins by bloorthogonal modification offers a convenient pathway to create, modify, and study biologically active biopolymers. In this paper the Staudinger reaction of aryl-phosphonites for the chemoselective functionalization of azido-peptides and proteins was probed. Different water-soluble phosphonites with ollgoethylene substituents were synthesized and reacted with unprotected azido-containing peptides in aqueous systems at room temperature in high conversions. Finally, the Staudinger-phosphonite reaction was successfully applied to the site-specific modification of the protein calmodulin.

  DOI：

  10.1021/ol2020175