(3bS,6aS)-5,5-dimethyl-6a,7-dihydro-3bH-[1,3]dioxolo[4',5':3,4]pyrrolo[1,2-c][1,2,3]triazole | 1373038-72-2

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: (3bS,6aS)-5,5-dimethyl-6a,7-dihydro-3bH-[1,3]dioxolo[4',5':3,4]pyrrolo[1,2-c][1,2,3]triazole
• 英文别名: (2S,6S)-4,4-dimethyl-3,5-dioxa-8,9,10-triazatricyclo[6.3.0.02,6]undeca-1(11),9-diene
• CAS: 1373038-72-2
• 化学式: C₈H₁₁N₃O₂
• 分子量: 181.194
• InChiKey: ADGYAVCJPDPNIP-BQBZGAKWSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -0.5
• 重原子数：
  13
• 可旋转键数：
  0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.75
• 拓扑面积：
  49.2
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  (4S,5S)-4-(azidomethyl)-5-ethynyl-2,2-dimethyl-1,3-dioxolane 以 水 为溶剂， 反应 1.0h， 以61%的产率得到(3bS,6aS)-5,5-dimethyl-6a,7-dihydro-3bH-[1,3]dioxolo[4',5':3,4]pyrrolo[1,2-c][1,2,3]triazole
  参考文献：
  名称：

  Intramolecular Huisgen [3+2] cycloaddition in water: synthesis of fused pyrrolidine–triazoles

  摘要：

  The intramolecular alkyne-azide Huisgen [3+2] cycloaddition reaction as a 'click-chemistry' reaction without a metal catalyst has been studied under aerobic conditions. The synthesis of various pyrrolidine-triazole hybrid compounds has also been achieved by using this intramolecular cycloaddition reaction in water with complete 1,5-regioselectivity. (C) 2012 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetasy.2012.02.011

文献信息

• Intramolecular Huisgen [3+2] cycloaddition in water: synthesis of fused pyrrolidine–triazoles
  作者：Indresh Kumar、Nisar A. Mir、Chandrashaker V. Rode、Basant P. Wakhloo

  DOI：10.1016/j.tetasy.2012.02.011

  日期：2012.2

  The intramolecular alkyne-azide Huisgen [3+2] cycloaddition reaction as a 'click-chemistry' reaction without a metal catalyst has been studied under aerobic conditions. The synthesis of various pyrrolidine-triazole hybrid compounds has also been achieved by using this intramolecular cycloaddition reaction in water with complete 1,5-regioselectivity. (C) 2012 Elsevier Ltd. All rights reserved.