3,3'-bis(1-(p-methoxyphenyl)-1H-1,2,3-triazol-4-yl)-1,1'-binaphthyl-2,2'-diyl (1-pyrrolidinyl)phosphonite | 1352522-87-2

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: 3,3'-bis(1-(p-methoxyphenyl)-1H-1,2,3-triazol-4-yl)-1,1'-binaphthyl-2,2'-diyl (1-pyrrolidinyl)phosphonite
• 英文别名: 1-(4-Methoxyphenyl)-4-[16-[1-(4-methoxyphenyl)triazol-4-yl]-13-pyrrolidin-1-yl-12,14-dioxa-13-phosphapentacyclo[13.8.0.02,11.03,8.018,23]tricosa-1(15),2(11),3,5,7,9,16,18,20,22-decaen-10-yl]triazole；1-(4-methoxyphenyl)-4-[16-[1-(4-methoxyphenyl)triazol-4-yl]-13-pyrrolidin-1-yl-12,14-dioxa-13-phosphapentacyclo[13.8.0.02,11.03,8.018,23]tricosa-1(15),2(11),3,5,7,9,16,18,20,22-decaen-10-yl]triazole
• CAS: 1352522-87-2
• 化学式: C₄₂H₃₄N₇O₄P
• 分子量: 731.75
• InChiKey: RNWOLVBLDBKHRL-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  8.7
• 重原子数：
  54
• 可旋转键数：
  7
• 环数：
  10.0
• sp3杂化的碳原子比例：
  0.14
• 拓扑面积：
  109
• 氢给体数：
  0
• 氢受体数：
  9

反应信息

• 作为产物：
  描述：

  3,3'-bis(1-(p-methoxyphenyl)-1H-1,2,3-triazol-4-yl)-2,2'-bis(methoxymethoxy)-1,1'-binaphthyl 在 盐酸 、 三氯化磷 作用下， 以 水 、 丙酮 、 甲苯 、 1,3-二氯苯 为溶剂， 反应 23.0h， 生成 3,3'-bis(1-(p-methoxyphenyl)-1H-1,2,3-triazol-4-yl)-1,1'-binaphthyl-2,2'-diyl (1-pyrrolidinyl)phosphonite 、 3,3'-bis(1-(p-methoxyphenyl)-1H-1,2,3-triazol-4-yl)-1,1'-binaphthyl-2,2'-diyl (1-pyrrolidinyl)phosphonate
  参考文献：
  名称：

  Synthesis of modified binol-phosphoramidites

  摘要：

  A number of chiral phosphoramidite ligands containing electronically different N-heterocycles at the 3,3'-positions of the binol scaffold were synthesized. The nucleophilicity of the pendant heterocycles correlated with the propensity of the P(III) centre to undergo aerobic oxidation to P(V). Due to an unexpected Staudinger-type reaction between the product phosphoramidites, the order in which the individual synthetic transformations were conducted was found to be important. The synthesis of a phosphoramidite ligand containing flanking groups at the 3,3'-positions of the binol scaffold in addition to a stereogenic phosphorus atom was also undertaken. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2011.11.020