((3aR,5S,6R,6aR)-6-hydroxy-2,2-dimethyl-tetrahydrofuro[2,3-d][1,3]dioxol-5-yl)methyl benzoselenoate | 1229341-70-1

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: ((3aR,5S,6R,6aR)-6-hydroxy-2,2-dimethyl-tetrahydrofuro[2,3-d][1,3]dioxol-5-yl)methyl benzoselenoate
• 英文别名: Se-[[(3aR,5S,6R,6aR)-6-hydroxy-2,2-dimethyl-3a,5,6,6a-tetrahydrofuro[2,3-d][1,3]dioxol-5-yl]methyl] benzenecarboselenoate
• CAS: 1229341-70-1
• 化学式: C₁₅H₁₈O₅Se
• 分子量: 357.265
• InChiKey: CUOOQHOIIFOARB-GFQSEFKGSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.19
• 重原子数：
  21
• 可旋转键数：
  4
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.53
• 拓扑面积：
  65
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为产物：
  描述：

  (3aR,3a'R,5S,5'S,6R,6aR,6'R,6a'R)-5,5'-diselanediylbis(methylene)bis(2,2-dimethyltetrahydrofuro[2,3-d][1,3]-dioxol-6-ol) 、 苯甲酰氯 在 sodium tetrahydroborate 作用下， 以 四氢呋喃 、 乙醇 为溶剂， 反应 24.17h， 以95%的产率得到((3aR,5S,6R,6aR)-6-hydroxy-2,2-dimethyl-tetrahydrofuro[2,3-d][1,3]dioxol-5-yl)methyl benzoselenoate
  参考文献：
  名称：

  Synthesis of 5′-seleno-xylofuranosides

  摘要：

  The synthesis of selenium derivatives of naturally occurring chiral molecules is becoming increasingly important in recent years. In this context, we describe herein an easy, straightforward synthetic route for the preparation of a series of chiral seleno-furanosides, starting from the readily available carbohydrate D-xylose. In addition, selected compounds were screened as inhibitors of the delta-aminolevulinate dehyclratase (delta-ALA-D) enzyme. Diselenide 4 was found to reduce significantly the enzymatic activity, while seleno-furanoside la increased delta-ALA-D activity. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2010.03.033