(2S,4S,5S)-5-allyl-4-(benzoyloxy)-1,2-pyrrolidinedicarboxylic acid 2-methyl 1-(2-(trimethylsilyl)ethyl) diester | 132592-24-6

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: (2S,4S,5S)-5-allyl-4-(benzoyloxy)-1,2-pyrrolidinedicarboxylic acid 2-methyl 1-(2-(trimethylsilyl)ethyl) diester
• 英文别名: (2S,4S,5S)-5-allyl-4-(benzoyloxy)-1,2-pyrrolidinedicarboxylic acid 2-methyl 1-[2-(trimethylsilyl)ethyl] diester；2-O-methyl 1-O-(2-trimethylsilylethyl) (2S,4S,5S)-4-benzoyloxy-5-prop-2-enylpyrrolidine-1,2-dicarboxylate
• CAS: 132592-24-6
• 化学式: C₂₂H₃₁NO₆Si
• 分子量: 433.577
• InChiKey: QFXOQCCSBPVIPS-FHWLQOOXSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.88
• 重原子数：
  30.0
• 可旋转键数：
  8.0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  82.14
• 氢给体数：
  0.0
• 氢受体数：
  6.0

反应信息

• 作为产物：
  描述：

  (2S,4S,5RS)-4,5-diacetoxy-1,2-pyrrolidinedicarboxylic acid 2-methyl 1-(2-(trimethylsilyl)ethyl) diester 在 4-二甲氨基吡啶 、 三氟甲磺酸三甲基硅酯 、 sodium methylate 、 三乙胺 作用下， 以 甲醇 、 二氯甲烷 为溶剂， 反应 17.25h， 生成 (2S,4S,5S)-5-allyl-4-(benzoyloxy)-1,2-pyrrolidinedicarboxylic acid 2-methyl 1-(2-(trimethylsilyl)ethyl) diester
  参考文献：
  名称：

  Electrochemical oxidation of proline derivatives: total syntheses of bulgecinine and bulgecin C

  摘要：

  The influence of structure on the efficiency of the electrochemical C-5 oxidation of (2S,4S)-hydroxyproline carbamate esters is presented. Optimum methoxylation was observed with (2S,4S)-4-acetoxy-1,2-pyrrolidine-dicarboxylic acid 2-methyl 1-(2-(trimethylsily)ethyl) ester (19). The corresponding C-5 methoxy derivative 20 was converted into bulgecinine (4) via a stereospecific radical homologation to incorporate the C-5 hydroxymethyl substituent. Bulgecin C (1c) was prepared via a beta-stereoselective glycosidation reaction using a 2-azido-2-deoxy-alpha-D-glucopyranosyl trichloroacetimidate derivative, regiospecific C-4' sulfation, and deprotection.

  DOI：

  10.1021/jo00008a040