O-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-(1->4)-O-(2,3,6-tri-O-acetyl-β-D-glucopyranosyl)-(1->3)-2,4-di-O-benzyl-1-thio-α-D-glucopyranose | 1350618-96-0

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: O-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-(1->4)-O-(2,3,6-tri-O-acetyl-β-D-glucopyranosyl)-(1->3)-2,4-di-O-benzyl-1-thio-α-D-glucopyranose
• 英文别名: Glc2Ac3Ac4Ac6Ac(a1-4)Glc2Ac3Ac6Ac(b1-3)[Bn(-2)][Bn(-4)]a-Glc1SH；[(2R,3R,4S,5R,6S)-4,5-diacetyloxy-6-[(2R,3R,4S,5R,6R)-2-(hydroxymethyl)-3,5-bis(phenylmethoxy)-6-sulfanyloxan-4-yl]oxy-3-[(2R,3R,4S,5R,6R)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxyoxan-2-yl]methyl acetate
• CAS: 1350618-96-0
• 化学式: C₄₆H₅₈O₂₂S
• 分子量: 995.019
• InChiKey: HDSVVHKKLFZGOI-FGKQJBOISA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.6
• 重原子数：
  69
• 可旋转键数：
  27
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.59
• 拓扑面积：
  270
• 氢给体数：
  2
• 氢受体数：
  23

反应信息

• 作为产物：
  描述：

  1,6-脱水-2,4-O-苯基-Β-D-吡喃葡萄糖 在 双(三甲基硫化硅) 、 三氟甲磺酸三甲基硅酯 、 silver trifluoromethanesulfonate 作用下， 以 二氯甲烷 为溶剂， 生成 O-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-(1->4)-O-(2,3,6-tri-O-acetyl-β-D-glucopyranosyl)-(1->3)-2,4-di-O-benzyl-1-thio-α-D-glucopyranose
  参考文献：
  名称：

  Synthesis of α-Glycosyl Thiols by Stereospecific Ring-Opening of 1,6-Anhydrosugars

  摘要：

  Treatment of 1,6-anhydrosugars with commercially available bis(trimethylsilyl) sulfide in the presence of trimethylsilyl triflate led to the formation of a-glycosyl thiols. All the reactions were highly stereoselective and afforded the a-glycosyl thiols in good to excellent yields. By this procedure, a variety of 1,6-anhydrosugars, differing in their sugar units, glycosidic linkages, and protecting group pattern, were converted smoothly into the corresponding a-glycosyl thiols, which could be of great utility in thioglycoside chemistry. It is noteworthy that 1,6-anhydrosugars carrying the 2-O-acyl group and 1,6-anhydrosugar-containing oligosaccharides could also be ring-opened stereospecifically under the same conditions to give rise to the corresponding 1-thiosugars in high yields. Thus, a very concise and efficient access to a-glycosyl thiols of great value was established.

  DOI：

  10.1021/jo202069y