5-(benzyloxy)-8-(tert-butoxycarbonyl)-3,3-dichloro-3a-methyl-8a-<(2,2-dimethylpropyl)sulfenyl>-3,3a,8,8a-tetrahydro-2H-furo<2,3-b>indol-2-one | 141613-17-4

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吲哚及其衍生物
• 英文名称: 5-(benzyloxy)-8-(tert-butoxycarbonyl)-3,3-dichloro-3a-methyl-8a-<(2,2-dimethylpropyl)sulfenyl>-3,3a,8,8a-tetrahydro-2H-furo<2,3-b>indol-2-one
• 英文别名: 5-(benzyloxy)-8-(tert-butoxycarbonyl)-3,3-dichloro-3a-methyl-8a-[(2,2-dimethylpropyl)sulfenyl]-3,3a,8,8a-tetrahydro-2H-furo[2,3-b]indol-2-one
• CAS: 141613-17-4
• 化学式: C₂₈H₃₃Cl₂NO₅S
• 分子量: 566.546
• InChiKey: LPONIBUNIHFAHT-HSLSYKTRSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  7.44
• 重原子数：
  37.0
• 可旋转键数：
  5.0
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  65.07
• 氢给体数：
  0.0
• 氢受体数：
  6.0

反应信息

• 作为反应物：
  描述：

  5-(benzyloxy)-8-(tert-butoxycarbonyl)-3,3-dichloro-3a-methyl-8a-<(2,2-dimethylpropyl)sulfenyl>-3,3a,8,8a-tetrahydro-2H-furo<2,3-b>indol-2-one 在 偶氮二异丁腈 、 三正丁基氢锡 作用下， 以 甲苯 为溶剂， 反应 48.0h， 生成 (-)-5-(benzyloxy)-8-(tert-butoxycarbonyl)-3a-methyl-3,3a,8,8a-tetrahydro-2H-furo<2,3-b>indol-2-one 、 (-)-5-(benzyloxy)-8-(tert-butoxycarbonyl)-3a-methyl-3,3a,8,8a-tetrahydro-2H-furo<2,3-b>indol-2-one
  参考文献：
  名称：

  The enantioselective synthesis of (-)-physostigmine via chiral sulfoxides

  摘要：

  The total synthesis of naturally occurring (-)-physostigmine is described. The key element for the asymmetric induction is the chirality transfer from optically active 2-(alkylsulfinyl)indoles to indoline butyrolactones bearing two chiral centers. Novel features of this synthesis involve the use of a new class of sulfoxylating agents, N-(alkylsulfinyl)oxazolidinones, to prepare the starting indolyl sulfoxides and the correlation of the size of the alkyl group on the sulfoxide with the degree of asymmetric induction. The overall synthesis requires a dozen steps from commercially available 5-(benzyloxy)indole.

  DOI：

  10.1021/ja00040a013
• 作为产物：
  描述：

  3-甲基-5-苯甲氧基-1H-吲哚 在 4-二甲氨基吡啶 、 仲丁基锂 、 三乙胺 、 copper(l) chloride 、 锌 作用下， 以 四氢呋喃 为溶剂， 反应 4.25h， 生成 5-(benzyloxy)-8-(tert-butoxycarbonyl)-3,3-dichloro-3a-methyl-8a-<(2,2-dimethylpropyl)sulfenyl>-3,3a,8,8a-tetrahydro-2H-furo<2,3-b>indol-2-one
  参考文献：
  名称：

  The enantioselective synthesis of (-)-physostigmine via chiral sulfoxides

  摘要：

  The total synthesis of naturally occurring (-)-physostigmine is described. The key element for the asymmetric induction is the chirality transfer from optically active 2-(alkylsulfinyl)indoles to indoline butyrolactones bearing two chiral centers. Novel features of this synthesis involve the use of a new class of sulfoxylating agents, N-(alkylsulfinyl)oxazolidinones, to prepare the starting indolyl sulfoxides and the correlation of the size of the alkyl group on the sulfoxide with the degree of asymmetric induction. The overall synthesis requires a dozen steps from commercially available 5-(benzyloxy)indole.

  DOI：

  10.1021/ja00040a013