methyl 2-[(1S,2R,3R,4S,5R,6S)-3,4,5-tris(phenylmethoxy)-7-oxabicyclo[4.1.0]heptan-2-yl]acetate | 215303-30-3

• 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: methyl 2-[(1S,2R,3R,4S,5R,6S)-3,4,5-tris(phenylmethoxy)-7-oxabicyclo[4.1.0]heptan-2-yl]acetate
• CAS: 215303-30-3
• 化学式: C₃₀H₃₂O₆
• 分子量: 488.58
• InChiKey: IDIRFXPAPPORAU-URBZSDFSSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.1
• 重原子数：
  36
• 可旋转键数：
  12
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.37
• 拓扑面积：
  66.5
• 氢给体数：
  0
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  methyl 2-[(1S,2R,3R,4S,5R,6S)-3,4,5-tris(phenylmethoxy)-7-oxabicyclo[4.1.0]heptan-2-yl]acetate 在 potassium carbonate 作用下， 以 甲醇 、 水 为溶剂， 反应 20.0h， 以78%的产率得到((1S,2R,3S,4S,5S,6R)-2,3,4-Tris-benzyloxy-5,6-dihydroxy-cyclohexyl)-acetic acid
  参考文献：
  名称：

  Free Radical Studies and Solutions to the Synthesis of (+)-Cyclophellitol

  摘要：

  D-Xylose serves as a starting material for approaches to the synthesis of the glucosidase inhibitors, (+)-cyclophellitol (1) and (+)-epi-cyclophellitol (2). An investigation of the cyclization of diastereomeric oxiranyl radicals to achieve this goal was moderately successful with the diastereomer that would have led to epi-cyclophellitol undergoing cyclization. An alternative route to cyclophellitol from D-xylose employed Grubbs' ring closure metathesis and radical transformations to complete the synthesis.

  DOI：

  10.1021/jo981211d
• 作为产物：
  描述：

  (2R,3R)-3-[(E,1R,2S,3R)-6-methoxy-6-oxo-1,2,3-tris(phenylmethoxy)hex-4-enyl]oxirane-2-carboxylic acid 在 N-甲基吗啉 、 三正丁基氢锡 、 氯甲酸异丁酯 作用下， 以 四氢呋喃 为溶剂， 反应 3.58h， 生成 methyl 2-[(1S,2R,3R,4S,5R,6S)-3,4,5-tris(phenylmethoxy)-7-oxabicyclo[4.1.0]heptan-2-yl]acetate
  参考文献：
  名称：

  Free Radical Studies and Solutions to the Synthesis of (+)-Cyclophellitol

  摘要：

  D-Xylose serves as a starting material for approaches to the synthesis of the glucosidase inhibitors, (+)-cyclophellitol (1) and (+)-epi-cyclophellitol (2). An investigation of the cyclization of diastereomeric oxiranyl radicals to achieve this goal was moderately successful with the diastereomer that would have led to epi-cyclophellitol undergoing cyclization. An alternative route to cyclophellitol from D-xylose employed Grubbs' ring closure metathesis and radical transformations to complete the synthesis.

  DOI：

  10.1021/jo981211d

文献信息

• Free Radical Studies and Solutions to the Synthesis of (+)-Cyclophellitol
  作者：Frederick E. Ziegler、Yizhe Wang

  DOI：10.1021/jo981211d

  日期：1998.10.1

  D-Xylose serves as a starting material for approaches to the synthesis of the glucosidase inhibitors, (+)-cyclophellitol (1) and (+)-epi-cyclophellitol (2). An investigation of the cyclization of diastereomeric oxiranyl radicals to achieve this goal was moderately successful with the diastereomer that would have led to epi-cyclophellitol undergoing cyclization. An alternative route to cyclophellitol from D-xylose employed Grubbs' ring closure metathesis and radical transformations to complete the synthesis.