2-(trimethylsilyl)ethyl 3-O-benzoyl-2-deoxy-6-O-(p-methoxybenzoyl)-α-D-arabino-hexopyranoside

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 2-(trimethylsilyl)ethyl 3-O-benzoyl-2-deoxy-6-O-(p-methoxybenzoyl)-α-D-arabino-hexopyranoside
• 英文别名: [(2R,3S,4R,6S)-4-benzoyloxy-3-hydroxy-6-(2-trimethylsilylethoxy)oxan-2-yl]methyl 4-methoxybenzoate
• 化学式: C₂₆H₃₄O₈Si
• 分子量: 502.637
• InChiKey: UVVRDCABYRFCEZ-LWSSLDFYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.91
• 重原子数：
  35
• 可旋转键数：
  12
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.46
• 拓扑面积：
  101
• 氢给体数：
  1
• 氢受体数：
  8

反应信息

• 作为产物：
  描述：

  2-(trimethylsilyl)ethyl β-D-glucopyranoside 在 potassium fluoride 、 偶氮二异丁腈 、 三正丁基氢锡 、 silver trifluoromethanesulfonate 、 对甲苯磺酸 、 silver nitrate 、 溶剂黄146 、 三乙胺 、 2,3-二氯-5,6-二氰基-1,4-苯醌 作用下， 以 吡啶 、 二氯甲烷 、 水 、 甲苯 、 乙腈 、 苯 为溶剂， 反应 20.0h， 生成 2-(trimethylsilyl)ethyl 3-O-benzoyl-2-deoxy-6-O-(p-methoxybenzoyl)-α-D-arabino-hexopyranoside
  参考文献：
  名称：

  Synthesis of Double-Chain Bis-Sulfone Neoglycolipids of the 2-, 3-, and 6-Deoxyglobotrioses

  摘要：

  Partially protected 2-(trimethylsilyl)ethyl 2- and 3-deoxyglucosides and 6-deoxylactoside were synthesised via various routes and glycosylated with galabiosyl and galactosyl donors to give the corresponding deoxytrisaccharides. Removal of the protecting groups gave the 2-(trimethylsilyl)ethyl 2-, 3-, and 6-deoxyglobotriosides. Transformation of the protected trisaccharides into trichloroacetimidates, via the corresponding hemiacetals, proceeded in similar to 80% overall yield. Glycosylation of 3-(hexadecylsulfonyl)-2-[(hexadecylsulfonyl)methyl]propanol with the trisaccharidic trichloroacetimidates, in 72-79% yield, followed by removal of protecting groups, gave the title neoglycolipids.

  DOI：

  10.1021/jo951914k

文献信息

• Synthesis of Double-Chain Bis-Sulfone Neoglycolipids of the 2-, 3-, and 6-Deoxyglobotrioses
  作者：Zhiyuan Zhang、Göran Magnusson

  DOI：10.1021/jo951914k

  日期：1996.1.1

  Partially protected 2-(trimethylsilyl)ethyl 2- and 3-deoxyglucosides and 6-deoxylactoside were synthesised via various routes and glycosylated with galabiosyl and galactosyl donors to give the corresponding deoxytrisaccharides. Removal of the protecting groups gave the 2-(trimethylsilyl)ethyl 2-, 3-, and 6-deoxyglobotriosides. Transformation of the protected trisaccharides into trichloroacetimidates, via the corresponding hemiacetals, proceeded in similar to 80% overall yield. Glycosylation of 3-(hexadecylsulfonyl)-2-[(hexadecylsulfonyl)methyl]propanol with the trisaccharidic trichloroacetimidates, in 72-79% yield, followed by removal of protecting groups, gave the title neoglycolipids.