(4R,4aR,6R,7S,7aS)-4,7-dimethyl-2-(toluene-4-sulfonyl)octahydro[2]pyrindin-6-ol | 1192544-87-8

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: (4R,4aR,6R,7S,7aS)-4,7-dimethyl-2-(toluene-4-sulfonyl)octahydro[2]pyrindin-6-ol
• 英文别名: (4R,4aR,6R,7S,7aS)-4,7-dimethyl-2-(4-methylphenyl)sulfonyl-1,3,4,4a,5,6,7,7a-octahydrocyclopenta[c]pyridin-6-ol
• CAS: 1192544-87-8
• 化学式: C₁₇H₂₅NO₃S
• 分子量: 323.456
• InChiKey: XMMILOKWPCEUEL-UQFXTHDASA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.8
• 重原子数：
  22
• 可旋转键数：
  2
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.65
• 拓扑面积：
  66
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  (4R,4aR,6R,7S,7aS)-4,7-dimethyl-2-(toluene-4-sulfonyl)octahydro[2]pyrindin-6-ol 在 氨 、 lithium 作用下， 以 四氢呋喃 为溶剂， 反应 1.0h， 生成 (4R,4aR,6R,7S,7aS)-4,7-dimethyl-2,3,4,4a,5,6,7,7a-octahydro-1H-cyclopenta[c]pyridin-6-ol
  参考文献：
  名称：

  Stereocontrolled preparation of bicyclic alkaloid analogues: an approach towards the kinabalurine skeleton

  摘要：

  An approach towards the construction of bicyclic analogues of monoterpene alkaloids belonging to the kinabalurine, incarvilline and skytanthine families Of natural products is reported These syntheses rely oil a stereoselective intramolecular Pauson-Khand cyclisation of a chiral pool-derived enyne in order to prepare the bicyclic core Stereoselective further elaboration generates diastereomeric analogues of the naturally occurring alkaloids (C) 2009 Elsevier Ltd All rights reserved

  DOI：

  10.1016/j.tet.2009.07.060
• 作为产物：
  描述：

  (4R,4aR,7S,7aS)-4,7-dimethyl-2-(toluene-4-sulfonyl)octahydro[2]pyrindin-6-one 在 sodium tetrahydroborate 、 水 作用下， 以 甲醇 为溶剂， 以45%的产率得到(4R,4aR,6R,7S,7aS)-4,7-dimethyl-2-(toluene-4-sulfonyl)octahydro[2]pyrindin-6-ol
  参考文献：
  名称：

  Stereocontrolled preparation of bicyclic alkaloid analogues: an approach towards the kinabalurine skeleton

  摘要：

  An approach towards the construction of bicyclic analogues of monoterpene alkaloids belonging to the kinabalurine, incarvilline and skytanthine families Of natural products is reported These syntheses rely oil a stereoselective intramolecular Pauson-Khand cyclisation of a chiral pool-derived enyne in order to prepare the bicyclic core Stereoselective further elaboration generates diastereomeric analogues of the naturally occurring alkaloids (C) 2009 Elsevier Ltd All rights reserved

  DOI：

  10.1016/j.tet.2009.07.060