(2S,3aR,6R,7S,7aR)-3a-Benzoyloxy-7-(tert-butyl-dimethyl-silanyloxy)-6-hydroxy-2,3,3a,6,7,7a-hexahydro-indole-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester | 185394-46-1

• 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,3aR,6R,7S,7aR)-3a-Benzoyloxy-7-(tert-butyl-dimethyl-silanyloxy)-6-hydroxy-2,3,3a,6,7,7a-hexahydro-indole-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester
• 英文别名: 1-O-benzyl 2-O-methyl (2S,3aR,6R,7S,7aR)-3a-benzoyloxy-7-[tert-butyl(dimethyl)silyl]oxy-6-hydroxy-3,6,7,7a-tetrahydro-2H-indole-1,2-dicarboxylate
• CAS: 185394-46-1
• 化学式: C₃₁H₃₉NO₈Si
• 分子量: 581.738
• InChiKey: GAELTAPPGLUOKL-JDBVQUIYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.86
• 重原子数：
  41
• 可旋转键数：
  11
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.45
• 拓扑面积：
  112
• 氢给体数：
  1
• 氢受体数：
  8

反应信息

• 作为反应物：
  描述：

  (2S,3aR,6R,7S,7aR)-3a-Benzoyloxy-7-(tert-butyl-dimethyl-silanyloxy)-6-hydroxy-2,3,3a,6,7,7a-hexahydro-indole-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester 在 4-二甲氨基吡啶 、 disodium hydrogenphosphate 、 sodium amalgam 、 三乙胺 作用下， 以 四氢呋喃 、 甲醇 、 二氯甲烷 为溶剂， 反应 4.5h， 生成 (2S,7R,7aS)-7-(tert-Butyl-dimethyl-silanyloxy)-2,3,7,7a-tetrahydro-indole-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester
  参考文献：
  名称：

  Stereodivergent routes from tyrosine to the 7-(R) and 7-(S) diastereomers of the 7-hydroxy-2,3,7,7a-tetrahydroindole ring found in gliotoxin

  摘要：

  Two routes from the oxidative cyclization product 1 derived from tyrosine to methyl 7-(tert-butyldimethylsiloxy)-N-(benzyloxycarbonyl) -2,3,7,7a-tetrahydroindole-2-carboxylate are described. The routes are stereodivergent leading to the 2-S,7-S,7a-S (6) and 2-S,7-R,7a-S-(13) diasteromers. The former stereochemistry corresponds to that present in gliotoxin. Copyright (C) 1996 Elsevier Science Ltd

  DOI：

  10.1016/0040-4020(96)00871-x
• 作为产物：
  描述：

  (2S,3aR,7S,7aR)-3a-Benzoyloxy-7-(tert-butyl-dimethyl-silanyloxy)-6-oxo-2,3,3a,6,7,7a-hexahydro-indole-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester 在 sodium tetrahydroborate 、 cerium(III) chloride 作用下， 以 四氢呋喃 为溶剂， 反应 0.08h， 以100%的产率得到(2S,3aR,6R,7S,7aR)-3a-Benzoyloxy-7-(tert-butyl-dimethyl-silanyloxy)-6-hydroxy-2,3,3a,6,7,7a-hexahydro-indole-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester
  参考文献：
  名称：

  Stereodivergent routes from tyrosine to the 7-(R) and 7-(S) diastereomers of the 7-hydroxy-2,3,7,7a-tetrahydroindole ring found in gliotoxin

  摘要：

  Two routes from the oxidative cyclization product 1 derived from tyrosine to methyl 7-(tert-butyldimethylsiloxy)-N-(benzyloxycarbonyl) -2,3,7,7a-tetrahydroindole-2-carboxylate are described. The routes are stereodivergent leading to the 2-S,7-S,7a-S (6) and 2-S,7-R,7a-S-(13) diasteromers. The former stereochemistry corresponds to that present in gliotoxin. Copyright (C) 1996 Elsevier Science Ltd

  DOI：

  10.1016/0040-4020(96)00871-x

文献信息

• Stereodivergent routes from tyrosine to the 7-(R) and 7-(S) diastereomers of the 7-hydroxy-2,3,7,7a-tetrahydroindole ring found in gliotoxin
  作者：Todd C Henninger、Michal Sabat、Richard J Sundberg

  DOI：10.1016/0040-4020(96)00871-x

  日期：1996.11

  Two routes from the oxidative cyclization product 1 derived from tyrosine to methyl 7-(tert-butyldimethylsiloxy)-N-(benzyloxycarbonyl) -2,3,7,7a-tetrahydroindole-2-carboxylate are described. The routes are stereodivergent leading to the 2-S,7-S,7a-S (6) and 2-S,7-R,7a-S-(13) diasteromers. The former stereochemistry corresponds to that present in gliotoxin. Copyright (C) 1996 Elsevier Science Ltd