[(3S,4R)-3,4,5-tribenzoyloxyoxolan-3-yl]methyl benzoate | 1309453-98-2

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: [(3S,4R)-3,4,5-tribenzoyloxyoxolan-3-yl]methyl benzoate
• CAS: 1309453-98-2
• 化学式: C₃₃H₂₆O₉
• 分子量: 566.564
• InChiKey: GXYUBZXKZKDELI-ATPTUWPCSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.2
• 重原子数：
  42
• 可旋转键数：
  13
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.15
• 拓扑面积：
  114
• 氢给体数：
  0
• 氢受体数：
  9

反应信息

• 作为反应物：
  描述：

  [(3S,4R)-3,4,5-tribenzoyloxyoxolan-3-yl]methyl benzoate 在 氢溴酸 作用下， 以 二氯甲烷 、 溶剂黄146 为溶剂， 生成 2,3,5-tri-O-benzoyl-α/β-D-apiofuranosyl bromide
  参考文献：
  名称：

  Synthesis of quercetin 3-O-β-d-apiofuranosyl-(1→2)-[α-l-rhamnopyranosyl-(1→6)]-β-d-glucopyranoside

  摘要：

  A concise method to construct a unique 2,6-branched trisaccharide was established by regioselective glycosylation of three free hydroxyl groups on a 3-O-protected glucose moiety, and successfully used in the synthesis of quercetin 3-O-beta-D-apiofuranosyl-(1 -> 2)-[alpha-L-rhamnopyranosyl-(1 -> 6)]-beta-D-glucopyranoside, a flavonol O-glycoside isolated from glandless cotton seeds which showed notable antidepressant activities. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2011.04.040
• 作为产物：
  描述：

  3-C-hydroxymethyl-2,3-O-isopropylidene-β-D-erythrofuranoside 在 吡啶 、 甲酸 作用下， 以 二氯甲烷 、 水 为溶剂， 反应 18.0h， 生成 [(3S,4R)-3,4,5-tribenzoyloxyoxolan-3-yl]methyl benzoate
  参考文献：
  名称：

  Synthesis of quercetin 3-O-β-d-apiofuranosyl-(1→2)-[α-l-rhamnopyranosyl-(1→6)]-β-d-glucopyranoside

  摘要：

  A concise method to construct a unique 2,6-branched trisaccharide was established by regioselective glycosylation of three free hydroxyl groups on a 3-O-protected glucose moiety, and successfully used in the synthesis of quercetin 3-O-beta-D-apiofuranosyl-(1 -> 2)-[alpha-L-rhamnopyranosyl-(1 -> 6)]-beta-D-glucopyranoside, a flavonol O-glycoside isolated from glandless cotton seeds which showed notable antidepressant activities. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2011.04.040