(1S,10R,10aR)-10-(tert-butoxycarbonylmethyl)-1-triethylsilyloxy-7,8-methylenedioxy-1,2,3,5,10,10a-hexahydrobenz[f]indolizidine | 244260-73-9

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 四氢异喹啉
• 英文名称: (1S,10R,10aR)-10-(tert-butoxycarbonylmethyl)-1-triethylsilyloxy-7,8-methylenedioxy-1,2,3,5,10,10a-hexahydrobenz[f]indolizidine
• 英文别名: tert-butyl 2-[(9S,9aR,10R)-9-triethylsilyloxy-5,7,8,9,9a,10-hexahydro-[1,3]benzodioxolo[5,6-f]indolizin-10-yl]acetate
• CAS: 244260-73-9
• 化学式: C₂₅H₃₉NO₅Si
• 分子量: 461.674
• InChiKey: WESLMQLICOLZSB-JXALWOEJSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.21
• 重原子数：
  32
• 可旋转键数：
  9
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.72
• 拓扑面积：
  57.2
• 氢给体数：
  0
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  (1S,10R,10aR)-10-(tert-butoxycarbonylmethyl)-1-triethylsilyloxy-7,8-methylenedioxy-1,2,3,5,10,10a-hexahydrobenz[f]indolizidine 在 吡啶 、 盐酸 、 正丁基锂 、 二异丁基氢化铝 作用下， 以 四氢呋喃 、 正己烷 、 二氯甲烷 为溶剂， 反应 3.09h， 生成 (1S,10R,10aR,2'S)-10-(2'-acetoxy-4'-trimethylsilyl-3'-butynyl)-1-hydroxy-7,8-methylenedioxy-1,2,3,5,10,10a-hexahydrobenz[f]indolizidine
  参考文献：
  名称：

  Synthesis of Optically Active 2-Acetoxy-3-alkylidene-a-lycoranes for a Synthetic Approach toward (+)-Lycorine by Radical Reaction

  摘要：

  A radical-mediated synthesis of optically active 2alpha- and 2beta-trimethylsilylmethyene-alpha-lycoranes (3,4), which are key intermediates for synthesis of (+)- lycorine (2), is described. Thus, both B and C rings in lycorine (2) were constructed by 6-exo mode radical cyclization. The former ring formation was performed in diastereoselective manner by radical cyclization via alpha-acylamino radical of (4S,5R)-4-acetoxy-N-(2-methoxy-, benzyloxy-, and tert-butoxy-carbonylethenyl-4,5-methylenedioxybenzyl)- or (4S,5R)-N-(2-tert-butoxycarbonylethenyl-4,5-methylenedioxybenzyl)-4-triethyisilyloxy-5-phenyl- selenyl-2-pyrrolidinones (10-12 or 19). The latter ring formation was accomplished by the reaction of (1S,10R,10aR,2'S)- and (1S,10R,10aR,2'R)-10-(2'-acetoxy-4'-trimethylsilyl-3'-butynyl)-1-imidazolylthiocarbonyloxy-7,8-methylenedioxy- 1,2,3,5, 10, 10a-hexahydrobenz[f]indolizidines (28).

  DOI：

  10.3987/com-02-9610
• 作为产物：
  描述：

  (4S,5R)-4-hydroxy-N-(2-iodo-4,5-methylenedioxybenzyl)-5-phenylselenyl-2-pyrrolidinone 在 吡啶 、 咪唑 、 硼烷四氢呋喃络合物 、 palladium(III) acetate 、 偶氮二异丁腈 、 三正丁基氢锡 、 三乙胺 、 三苯基膦 作用下， 以 四氢呋喃 、 N,N-二甲基甲酰胺 、 苯 为溶剂， 反应 42.5h， 生成 (1S,10R,10aR)-10-(tert-butoxycarbonylmethyl)-1-triethylsilyloxy-7,8-methylenedioxy-1,2,3,5,10,10a-hexahydrobenz[f]indolizidine
  参考文献：
  名称：

  Synthesis of Optically Active 2-Acetoxy-3-alkylidene-a-lycoranes for a Synthetic Approach toward (+)-Lycorine by Radical Reaction

  摘要：

  A radical-mediated synthesis of optically active 2alpha- and 2beta-trimethylsilylmethyene-alpha-lycoranes (3,4), which are key intermediates for synthesis of (+)- lycorine (2), is described. Thus, both B and C rings in lycorine (2) were constructed by 6-exo mode radical cyclization. The former ring formation was performed in diastereoselective manner by radical cyclization via alpha-acylamino radical of (4S,5R)-4-acetoxy-N-(2-methoxy-, benzyloxy-, and tert-butoxy-carbonylethenyl-4,5-methylenedioxybenzyl)- or (4S,5R)-N-(2-tert-butoxycarbonylethenyl-4,5-methylenedioxybenzyl)-4-triethyisilyloxy-5-phenyl- selenyl-2-pyrrolidinones (10-12 or 19). The latter ring formation was accomplished by the reaction of (1S,10R,10aR,2'S)- and (1S,10R,10aR,2'R)-10-(2'-acetoxy-4'-trimethylsilyl-3'-butynyl)-1-imidazolylthiocarbonyloxy-7,8-methylenedioxy- 1,2,3,5, 10, 10a-hexahydrobenz[f]indolizidines (28).

  DOI：

  10.3987/com-02-9610

文献信息

• Synthesis of Optically Active 2-Acetoxy-3-alkylidene-a-lycoranes for a Synthetic Approach toward (+)-Lycorine by Radical Reaction
  作者：Miyuki Ishizaki、Yuichiro Kai、Osamu Hoshino

  DOI：10.3987/com-02-9610

  日期：——

  A radical-mediated synthesis of optically active 2alpha- and 2beta-trimethylsilylmethyene-alpha-lycoranes (3,4), which are key intermediates for synthesis of (+)- lycorine (2), is described. Thus, both B and C rings in lycorine (2) were constructed by 6-exo mode radical cyclization. The former ring formation was performed in diastereoselective manner by radical cyclization via alpha-acylamino radical of (4S,5R)-4-acetoxy-N-(2-methoxy-, benzyloxy-, and tert-butoxy-carbonylethenyl-4,5-methylenedioxybenzyl)- or (4S,5R)-N-(2-tert-butoxycarbonylethenyl-4,5-methylenedioxybenzyl)-4-triethyisilyloxy-5-phenyl- selenyl-2-pyrrolidinones (10-12 or 19). The latter ring formation was accomplished by the reaction of (1S,10R,10aR,2'S)- and (1S,10R,10aR,2'R)-10-(2'-acetoxy-4'-trimethylsilyl-3'-butynyl)-1-imidazolylthiocarbonyloxy-7,8-methylenedioxy- 1,2,3,5, 10, 10a-hexahydrobenz[f]indolizidines (28).