6-O-benzoyl-N-(2,2-diethoxycarbonylvinyl)-2,3-O-isopropylidene-β-D-mannofuranosylamine | 750586-78-8

• 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: 6-O-benzoyl-N-(2,2-diethoxycarbonylvinyl)-2,3-O-isopropylidene-β-D-mannofuranosylamine
• 英文别名: diethyl 2-[[[(3aS,4R,6R,6aS)-6-[(1R)-2-benzoyloxy-1-hydroxyethyl]-2,2-dimethyl-3a,4,6,6a-tetrahydrofuro[3,4-d][1,3]dioxol-4-yl]amino]methylidene]propanedioate
• CAS: 750586-78-8
• 化学式: C₂₄H₃₁NO₁₀
• 分子量: 493.511
• InChiKey: PTECIMHXWWUHKP-SWBPCFCJSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.8
• 重原子数：
  35
• 可旋转键数：
  13
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.54
• 拓扑面积：
  139
• 氢给体数：
  2
• 氢受体数：
  11

反应信息

• 作为反应物：
  描述：

  6-O-benzoyl-N-(2,2-diethoxycarbonylvinyl)-2,3-O-isopropylidene-β-D-mannofuranosylamine 在 吡啶 、 sodium methylate 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 20.0~40.0 ℃ 、2.67 kPa 条件下， 反应 32.0h， 生成 1,5-anhydro-6-O-benzoyl-N-(2,2-diethoxycarbonylvinyl)-2,3-O-isopropylidene-α-L-gulofuranosylamine
  参考文献：
  名称：

  Ring contraction of glycopyranosyl enamines: an easy route to furanoid thioglycosides of 5-aminosugars

  摘要：

  The reaction of glycohexapyranosyl enamines, having 2- and 3-hydroxyl groups in a cis-relationship with 12-dimethoxypropane, induces ring contraction of the sugar ring with formation of 2,3-O-isopropylidene furanoid glycosylenamines. 5-O-Mesylation of these compounds. followed by formation of anhydroazasugars and nucleophilic ring opening, with thiols, produces alkyl and aryl thiofuranosides of 5-aminosugars. (C) 2004 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetasy.2004.05.027
• 作为产物：
  描述：

  N-(2,2-diethoxycarbonylvinyl)-β-D-mannopyranosylamine 在 吡啶 作用下， 以 丙酮 为溶剂， 反应 25.0h， 生成 6-O-benzoyl-N-(2,2-diethoxycarbonylvinyl)-2,3-O-isopropylidene-β-D-mannofuranosylamine
  参考文献：
  名称：

  Ring contraction of glycopyranosyl enamines: an easy route to furanoid thioglycosides of 5-aminosugars

  摘要：

  The reaction of glycohexapyranosyl enamines, having 2- and 3-hydroxyl groups in a cis-relationship with 12-dimethoxypropane, induces ring contraction of the sugar ring with formation of 2,3-O-isopropylidene furanoid glycosylenamines. 5-O-Mesylation of these compounds. followed by formation of anhydroazasugars and nucleophilic ring opening, with thiols, produces alkyl and aryl thiofuranosides of 5-aminosugars. (C) 2004 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetasy.2004.05.027

文献信息

• Ring contraction of glycopyranosyl enamines: an easy route to furanoid thioglycosides of 5-aminosugars
  作者：M.Ángeles Pradera、Francisco J. Sayago、José M. Illangua、Manuel Angulo、Consolación Gasch、José Fuentes

  DOI：10.1016/j.tetasy.2004.05.027

  日期：2004.7

  The reaction of glycohexapyranosyl enamines, having 2- and 3-hydroxyl groups in a cis-relationship with 12-dimethoxypropane, induces ring contraction of the sugar ring with formation of 2,3-O-isopropylidene furanoid glycosylenamines. 5-O-Mesylation of these compounds. followed by formation of anhydroazasugars and nucleophilic ring opening, with thiols, produces alkyl and aryl thiofuranosides of 5-aminosugars. (C) 2004 Elsevier Ltd. All rights reserved.