(2R,3R,4R,5S)-3,4-Bis-methoxymethoxy-2-trityloxymethyl-5-vinyl-pyrrolidine-1-carboxylic acid tert-butyl ester | 165879-60-7

• 分子结构分类: 有机化合物 - 苯类化合物 - 三苯基化合物
• 英文名称: (2R,3R,4R,5S)-3,4-Bis-methoxymethoxy-2-trityloxymethyl-5-vinyl-pyrrolidine-1-carboxylic acid tert-butyl ester
• CAS: 165879-60-7
• 化学式: C₃₅H₄₃NO₇
• 分子量: 589.729
• InChiKey: AQXWUILBIRSIOS-SYEZAVJTSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.15
• 重原子数：
  43.0
• 可旋转键数：
  13.0
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.4
• 拓扑面积：
  75.69
• 氢给体数：
  0.0
• 氢受体数：
  7.0

反应信息

• 作为反应物：
  描述：

  (2R,3R,4R,5S)-3,4-Bis-methoxymethoxy-2-trityloxymethyl-5-vinyl-pyrrolidine-1-carboxylic acid tert-butyl ester 在 sodium tetrahydroborate 、 臭氧 作用下， 生成 (2S,3R,4R,5R)-2-Hydroxymethyl-3,4-bis-methoxymethoxy-5-trityloxymethyl-pyrrolidine-1-carboxylic acid tert-butyl ester
  参考文献：
  名称：

  Synthesis of (2R, 3R, 4R, 5R)-3,4-Dihydroxy-2,5-dihydroxymethylpyrrolidine and (-)-Anisomycin Derivative from (S)-Pyroglutamic Acid Derivative

  摘要：

  Double asymmetric dihydroxylation of (E)-alpha,beta-unsaturated ester(2) with a catalytic amount of potassium osmate and chiral ligand gave dihydroxy compounds (3a and 4a) selectively. Polyhydroxylated pyrrolidines (10 and 14) were synthesized from corresponding methoxymethy ether (3c) and tert-butyl-dimethylsilyl ether(4d), respectively.

  DOI：

  10.3987/com-94-7016
• 作为产物：
  描述：

  tert-butyl N-[(2R,3R,4R)-5-hydroxy-3,4-bis(methoxymethoxy)-1-trityloxypentan-2-yl]carbamate 在 草酰氯 、 TEA 、 二甲基亚砜 、 甲基磺酰氯 、 三乙胺 作用下， 以 四氢呋喃 、 二氯甲烷 为溶剂， 反应 1.67h， 生成 (2R,3R,4R,5S)-3,4-Bis-methoxymethoxy-2-trityloxymethyl-5-vinyl-pyrrolidine-1-carboxylic acid tert-butyl ester
  参考文献：
  名称：

  Synthesis of (2R, 3R, 4R, 5R)-3,4-Dihydroxy-2,5-dihydroxymethylpyrrolidine and (-)-Anisomycin Derivative from (S)-Pyroglutamic Acid Derivative

  摘要：

  Double asymmetric dihydroxylation of (E)-alpha,beta-unsaturated ester(2) with a catalytic amount of potassium osmate and chiral ligand gave dihydroxy compounds (3a and 4a) selectively. Polyhydroxylated pyrrolidines (10 and 14) were synthesized from corresponding methoxymethy ether (3c) and tert-butyl-dimethylsilyl ether(4d), respectively.

  DOI：

  10.3987/com-94-7016