methyl (phenyl 7-O-benzoyl-4-O-t-butyldimethylsilyl-3-deoxy-8,9-O-isopropylidene-5-O-methoxymethyl-2-thio-β-D-glycero-D-galacto-2-nonulopyranosid)onate | 243866-41-3

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: methyl (phenyl 7-O-benzoyl-4-O-t-butyldimethylsilyl-3-deoxy-8,9-O-isopropylidene-5-O-methoxymethyl-2-thio-β-D-glycero-D-galacto-2-nonulopyranosid)onate
• 英文别名: methyl (2R,4S,5S,6R)-6-[(R)-benzoyloxy-[(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]methyl]-4-[tert-butyl(dimethyl)silyl]oxy-5-(methoxymethoxy)-2-phenylsulfanyloxane-2-carboxylate
• CAS: 243866-41-3
• 化学式: C₃₄H₄₈O₁₀SSi
• 分子量: 676.901
• InChiKey: PQTYHPQUGBIXDM-XWDKLUHHSA-N

物化性质

• 沸点：
  663.195±55.00 °C(Press: 760.00 Torr)(predicted)
• 密度：
  1.200±0.10 g/cm3(Temp: 25 °C; Press: 760 Torr)(predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  6.19
• 重原子数：
  46
• 可旋转键数：
  15
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.59
• 拓扑面积：
  133
• 氢给体数：
  0
• 氢受体数：
  11

反应信息

• 作为反应物：
  描述：

  methyl (phenyl 7-O-benzoyl-4-O-t-butyldimethylsilyl-3-deoxy-8,9-O-isopropylidene-5-O-methoxymethyl-2-thio-β-D-glycero-D-galacto-2-nonulopyranosid)onate 在 sodium methylate 作用下， 以 甲醇 为溶剂， 反应 12.0h， 以95%的产率得到methyl (phenyl 4-O-t-butyldimethylsilyl-3-deoxy-8,9-O-isopropylidene-5-O-methoxymethyl-2-thio-β-D-glycero-D-galacto-2-nonulopyranosid)onate
  参考文献：
  名称：

  Selective Protecting Method for the Individual Hydroxyl Groups of Kdn

  摘要：

  Selective protection for the individual hydroxyl groups of methyl (phenyl 3-deoxy2-thio-beta-D-glycero-D-galacto-2-nonulopyranodis)onate (2) was examined. The 4-, 5-, and 7-hydroxyl groups of methyl (phenyl 3-deoxy-8,9-O-isopropylidene-2-thio-beta-D-glycero-D-galacto-2-nonulopyranosid)onate (3) were found selectively to be protected by t-butyldimethylsilyl, methoxymethyl, and benzoyl groups, respectively. In order to obtain the 8- and 9-hydroxyl derivatives selectively, methyl (phenyl 4,5,7-tri-O-acetyl-9-O-t-butyldimethylsilyl-3-deoxy-2-thio-beta-D-glycero-D-galacto-2-nonulopyranosid)onate (12) and methyl (phenyl 4,5,7,8-tetra-O-benzyl-9-O-triphenylmethyl-3-deoxy-2-thio-beta-D-glycero-D-galacto-2-nonulopyranosid)onate (19) were prepared in moderate yields.

  DOI：

  10.1080/07328309908544026
• 作为产物：
  描述：

  methyl (phenyl 4-O-t-butyldimethylsilyl-3-deoxy-8,9-O-isopropylidene-2-thio-β-D-glycero-D-galacto-2-nonulopyranosid)onate 在 吡啶 、 4 A molecular sieve 、 phosphorus pentoxide 作用下， 以 二氯甲烷 为溶剂， 反应 9.0h， 生成 methyl (phenyl 7-O-benzoyl-4-O-t-butyldimethylsilyl-3-deoxy-8,9-O-isopropylidene-5-O-methoxymethyl-2-thio-β-D-glycero-D-galacto-2-nonulopyranosid)onate
  参考文献：
  名称：

  Selective Protecting Method for the Individual Hydroxyl Groups of Kdn

  摘要：

  Selective protection for the individual hydroxyl groups of methyl (phenyl 3-deoxy2-thio-beta-D-glycero-D-galacto-2-nonulopyranodis)onate (2) was examined. The 4-, 5-, and 7-hydroxyl groups of methyl (phenyl 3-deoxy-8,9-O-isopropylidene-2-thio-beta-D-glycero-D-galacto-2-nonulopyranosid)onate (3) were found selectively to be protected by t-butyldimethylsilyl, methoxymethyl, and benzoyl groups, respectively. In order to obtain the 8- and 9-hydroxyl derivatives selectively, methyl (phenyl 4,5,7-tri-O-acetyl-9-O-t-butyldimethylsilyl-3-deoxy-2-thio-beta-D-glycero-D-galacto-2-nonulopyranosid)onate (12) and methyl (phenyl 4,5,7,8-tetra-O-benzyl-9-O-triphenylmethyl-3-deoxy-2-thio-beta-D-glycero-D-galacto-2-nonulopyranosid)onate (19) were prepared in moderate yields.

  DOI：

  10.1080/07328309908544026

文献信息

• Selective Protecting Method for the Individual Hydroxyl Groups of Kdn
  作者：Shoji Akai、Takahiro Nakagawa、Yasuhiro Kajihara、Ken-ichi Sato

  DOI：10.1080/07328309908544026

  日期：1999.1

  Selective protection for the individual hydroxyl groups of methyl (phenyl 3-deoxy2-thio-beta-D-glycero-D-galacto-2-nonulopyranodis)onate (2) was examined. The 4-, 5-, and 7-hydroxyl groups of methyl (phenyl 3-deoxy-8,9-O-isopropylidene-2-thio-beta-D-glycero-D-galacto-2-nonulopyranosid)onate (3) were found selectively to be protected by t-butyldimethylsilyl, methoxymethyl, and benzoyl groups, respectively. In order to obtain the 8- and 9-hydroxyl derivatives selectively, methyl (phenyl 4,5,7-tri-O-acetyl-9-O-t-butyldimethylsilyl-3-deoxy-2-thio-beta-D-glycero-D-galacto-2-nonulopyranosid)onate (12) and methyl (phenyl 4,5,7,8-tetra-O-benzyl-9-O-triphenylmethyl-3-deoxy-2-thio-beta-D-glycero-D-galacto-2-nonulopyranosid)onate (19) were prepared in moderate yields.