Imidazole-1-carbothioic acid O-[((2S,3S,4S,5S,6S)-4,5-bis-benzyloxy-2-benzyloxymethyl-6-methoxy-tetrahydro-pyran-3-yl)-((2R,3S,4S,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yl)-methyl] ester | 503456-90-4

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: Imidazole-1-carbothioic acid O-[((2S,3S,4S,5S,6S)-4,5-bis-benzyloxy-2-benzyloxymethyl-6-methoxy-tetrahydro-pyran-3-yl)-((2R,3S,4S,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yl)-methyl] ester
• 英文别名: O-[[(2S,3R,4S,5S,6S)-6-methoxy-4,5-bis(phenylmethoxy)-2-(phenylmethoxymethyl)oxan-3-yl]-[(2R,3S,4S,5R,6R)-3,4,5-tris(phenylmethoxy)-6-(phenylmethoxymethyl)oxan-2-yl]methyl] imidazole-1-carbothioate
• CAS: 503456-90-4
• 化学式: C₆₇H₇₀N₂O₁₁S
• 分子量: 1111.37
• InChiKey: SBSSLUKYPLGIAD-LAPSQHNGSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  10.4
• 重原子数：
  81
• 可旋转键数：
  28
• 环数：
  10.0
• sp3杂化的碳原子比例：
  0.31
• 拓扑面积：
  151
• 氢给体数：
  0
• 氢受体数：
  13

反应信息

• 作为反应物：
  描述：

  Imidazole-1-carbothioic acid O-[((2S,3S,4S,5S,6S)-4,5-bis-benzyloxy-2-benzyloxymethyl-6-methoxy-tetrahydro-pyran-3-yl)-((2R,3S,4S,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yl)-methyl] ester 在 偶氮二异丁腈 、 五氟苯酚 、 三苯基氢化锡 作用下， 以 甲苯 为溶剂， 反应 3.0h， 以54%的产率得到methyl 2,3,6-tri-O-benzyl-4-deoxy-4-C-[(2',3',4',6'-tetra-O-benzyl-α-D-mannopyranosyl)methyl]-α-D-mannopyranoside
  参考文献：
  名称：

  Synthesis of the C-Linked Disaccharide α-d-Man-(1→4)-d-Man Employing a SmI₂-Mediated C-Glycosylation Step:  En Route to Cyclic C-Oligosaccharides

  摘要：

  Investigations are reported on the assembly of the C-linked disaccharide alpha-D-Man-(1-->4)-D-Man, representing the first steps in our projected synthesis of a cyclic C-oligomer containing repeating units of this C-dimer. The key step in this synthesis uses a SmI2-mediated coupling of 2,3,4,6-tetra-O-benzyl-alpha-D-mannopyranosyl 2'-pyridyl sulfone with a C4-formyl branched mannopyranoside unit, affording the C-disaccharide derivative with complete stereocontrol at the two new stereogenic centers. Subsequently, a modified tin hydride based deoxygenation produced the target carbohydrate analogue. The synthesis of the C4-formyl monosaccharide makes use of a stereoselective radical-based allylation followed by double bond migration and ozonolysis.

  DOI：

  10.1021/jo020585a
• 作为产物：
  描述：

  methyl 2,3,6-tri-O-benzoyl-α-D-mannopyranoside 在 rhodium(III) chloride 甲醇 、 samarium diiodide 、 过氧化双月桂酰 、 sodium methylate 、 sodium hydride 、 potassium carbonate 、 臭氧 作用下， 以 四氢呋喃 、 甲醇 、 乙醇 、 二氯甲烷 、 N,N-二甲基甲酰胺 、 乙腈 、 苯 为溶剂， 反应 8.84h， 生成 Imidazole-1-carbothioic acid O-[((2S,3S,4S,5S,6S)-4,5-bis-benzyloxy-2-benzyloxymethyl-6-methoxy-tetrahydro-pyran-3-yl)-((2R,3S,4S,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yl)-methyl] ester
  参考文献：
  名称：

  Synthesis of the C-Linked Disaccharide α-d-Man-(1→4)-d-Man Employing a SmI₂-Mediated C-Glycosylation Step:  En Route to Cyclic C-Oligosaccharides

  摘要：

  Investigations are reported on the assembly of the C-linked disaccharide alpha-D-Man-(1-->4)-D-Man, representing the first steps in our projected synthesis of a cyclic C-oligomer containing repeating units of this C-dimer. The key step in this synthesis uses a SmI2-mediated coupling of 2,3,4,6-tetra-O-benzyl-alpha-D-mannopyranosyl 2'-pyridyl sulfone with a C4-formyl branched mannopyranoside unit, affording the C-disaccharide derivative with complete stereocontrol at the two new stereogenic centers. Subsequently, a modified tin hydride based deoxygenation produced the target carbohydrate analogue. The synthesis of the C4-formyl monosaccharide makes use of a stereoselective radical-based allylation followed by double bond migration and ozonolysis.

  DOI：

  10.1021/jo020585a

文献信息

• Synthesis of the <i>C</i>-Linked Disaccharide α-<scp>d</scp>-Man-(1→4)-<scp>d</scp>-Man Employing a SmI₂-Mediated <i>C</i>-Glycosylation Step:  En Route to Cyclic <i>C</i>-Oligosaccharides
  作者：Lise Munch Mikkelsen、Troels Skrydstrup

  DOI：10.1021/jo020585a

  日期：2003.3.1

  Investigations are reported on the assembly of the C-linked disaccharide alpha-D-Man-(1-->4)-D-Man, representing the first steps in our projected synthesis of a cyclic C-oligomer containing repeating units of this C-dimer. The key step in this synthesis uses a SmI2-mediated coupling of 2,3,4,6-tetra-O-benzyl-alpha-D-mannopyranosyl 2'-pyridyl sulfone with a C4-formyl branched mannopyranoside unit, affording the C-disaccharide derivative with complete stereocontrol at the two new stereogenic centers. Subsequently, a modified tin hydride based deoxygenation produced the target carbohydrate analogue. The synthesis of the C4-formyl monosaccharide makes use of a stereoselective radical-based allylation followed by double bond migration and ozonolysis.