(3aR,4S,4aS,9aR)-4-hydroxydecahydrofuro[2,3-f]indolizine | 1023284-65-2

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吲哚里西啶
• 英文名称: (3aR,4S,4aS,9aR)-4-hydroxydecahydrofuro[2,3-f]indolizine
• 英文别名: (3aR,4S,4aS,9aR)-2,3,3a,4,4a,5,6,7,9,9a-decahydrofuro[2,3-f]indolizin-4-ol
• CAS: 1023284-65-2
• 化学式: C₁₀H₁₇NO₂
• 分子量: 183.25
• InChiKey: SRMWCKCACSBSBH-XKNYDFJKSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.3
• 重原子数：
  13
• 可旋转键数：
  0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  32.7
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  (3aR,4S,4aS,9aR)-4-hydroxyoctahydrofuro[2,3-f]indolizin-7(2H)-one 在 lithium aluminium tetrahydride 作用下， 以 四氢呋喃 为溶剂， 反应 3.0h， 以81%的产率得到(3aR,4S,4aS,9aR)-4-hydroxydecahydrofuro[2,3-f]indolizine
  参考文献：
  名称：

  Highly diastereoselective approach to novel tetrahydrofuran-fused indolizidinols: a one-step formation of three contiguous stereocenters

  摘要：

  A concise and very efficient route to enantiopure tetrahydrofuran-fused indolizidinols, which could be considered as protected new indolizidindiols, is described in two-steps sequence starting from the known furoindolizidindiones. The key-step of these transformations was the formation, in one operation, of THF indolizidinols containing a lactam function by simultaneous highly diastereoseleclive catalytic hydrogenation of the carbonyl function and the furan ring. During these investigations, numerous catalysts in different combinations were tested and the impact of substrates on the reduction profile is discussed. (C) 2008 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetasy.2008.01.013

文献信息

• Highly diastereoselective approach to novel tetrahydrofuran-fused indolizidinols: a one-step formation of three contiguous stereocenters
  作者：Peter Šafář、Jozefína Žúžiová、Mária Bobošíková、Štefan Marchalín、Nadežda Prónayová、Vincent Dalla、Adam Daïch

  DOI：10.1016/j.tetasy.2008.01.013

  日期：2008.3

  A concise and very efficient route to enantiopure tetrahydrofuran-fused indolizidinols, which could be considered as protected new indolizidindiols, is described in two-steps sequence starting from the known furoindolizidindiones. The key-step of these transformations was the formation, in one operation, of THF indolizidinols containing a lactam function by simultaneous highly diastereoseleclive catalytic hydrogenation of the carbonyl function and the furan ring. During these investigations, numerous catalysts in different combinations were tested and the impact of substrates on the reduction profile is discussed. (C) 2008 Elsevier Ltd. All rights reserved.