allyl 3-O-benzyl-2-O-(methyl 2,3,4-tri-O-benzyl-α-D-glucopyranosyluronate)-α-L-fucopyranoside | 1110650-26-4

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: allyl 3-O-benzyl-2-O-(methyl 2,3,4-tri-O-benzyl-α-D-glucopyranosyluronate)-α-L-fucopyranoside
• CAS: 1110650-26-4
• 化学式: C₄₄H₅₀O₁₁
• 分子量: 754.874
• InChiKey: MJNZXFQNLPHLGX-BUMTXEGGSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.92
• 重原子数：
  55.0
• 可旋转键数：
  18.0
• 环数：
  6.0
• sp3杂化的碳原子比例：
  0.39
• 拓扑面积：
  120.37
• 氢给体数：
  1.0
• 氢受体数：
  11.0

反应信息

• 作为反应物：
  描述：

  allyl 3-O-benzyl-2-O-(methyl 2,3,4-tri-O-benzyl-α-D-glucopyranosyluronate)-α-L-fucopyranoside 在 吡啶 、 三氧化硫吡啶 、 碳酸氢钠 作用下， 以 N,N-二甲基甲酰胺 、 甲醇 为溶剂， 反应 3.0h， 生成
  参考文献：
  名称：

  Stereoselective Synthesis of Di- and Trisaccharide Fucoidan Fragments Bearing α-D-Glucuronic Acid Residue∗

  摘要：

  The first stereoselective synthesis of disaccharide alpha-D-GlcA-(1 -> 2)-alpha-L-Fuc-OPr ( 1), trisaccharide (1 -> 3)-alpha-L-Fuc-[alpha-D-GlcA-(1 -> 2)]-alpha-L-Fuc-OPr(3), and their selectively O-sulfated derivatives 2 and 4 bearing sulfo-groups at O(4) of the fucose units has been performed. Compounds 1-4 represent the fragments of the chain of the fucoidan from Cladosiphon okamuranus brown seaweed. Glucuronylation by a series of selectively O-acetylated glucuronyl bromides was studied to obtain the target products. It has been found that 3-O-acetylated donor 6 is the most efficient agent for alpha-glycoside bond formation that can be connected with intramolecular remote participation of 3-O-acetyl group favoring alpha-stereoselectivity.

  DOI：

  10.1080/07328300802419865
• 作为产物：
  描述：

  allyl 2-O-(methyl 2,3,4-tri-O-benzyl-α-D-glucopyranosyluronate)-α-L-fucopyranoside 、 溴甲苯 在 四丁基溴化铵 、 二正丁基氧化锡 作用下， 以 甲苯 为溶剂， 反应 2.0h， 以84%的产率得到allyl 3-O-benzyl-2-O-(methyl 2,3,4-tri-O-benzyl-α-D-glucopyranosyluronate)-α-L-fucopyranoside
  参考文献：
  名称：

  Stereoselective Synthesis of Di- and Trisaccharide Fucoidan Fragments Bearing α-D-Glucuronic Acid Residue∗

  摘要：

  The first stereoselective synthesis of disaccharide alpha-D-GlcA-(1 -> 2)-alpha-L-Fuc-OPr ( 1), trisaccharide (1 -> 3)-alpha-L-Fuc-[alpha-D-GlcA-(1 -> 2)]-alpha-L-Fuc-OPr(3), and their selectively O-sulfated derivatives 2 and 4 bearing sulfo-groups at O(4) of the fucose units has been performed. Compounds 1-4 represent the fragments of the chain of the fucoidan from Cladosiphon okamuranus brown seaweed. Glucuronylation by a series of selectively O-acetylated glucuronyl bromides was studied to obtain the target products. It has been found that 3-O-acetylated donor 6 is the most efficient agent for alpha-glycoside bond formation that can be connected with intramolecular remote participation of 3-O-acetyl group favoring alpha-stereoselectivity.

  DOI：

  10.1080/07328300802419865