6-chlorohexyl 2-acetamido-4-O-[2,4-di-O-acetyl-6-O-pivaloyl-3-O-(4,6-O-benzylidene-2-deoxy-2-trichloroacetamido-β-D-glucopyranosyl)-β-D-galactopyranosyl]-6-O-benzyl-3-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-2-deoxy-β-D-glucopyranoside | 1392400-72-4

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 6-chlorohexyl 2-acetamido-4-O-[2,4-di-O-acetyl-6-O-pivaloyl-3-O-(4,6-O-benzylidene-2-deoxy-2-trichloroacetamido-β-D-glucopyranosyl)-β-D-galactopyranosyl]-6-O-benzyl-3-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-2-deoxy-β-D-glucopyranoside
• CAS: 1392400-72-4
• 化学式: C₆₅H₈₆Cl₄N₂O₂₈
• 分子量: 1485.21
• InChiKey: MTHKWWOLGBGMJW-MBCWYUCCSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.72
• 重原子数：
  99.0
• 可旋转键数：
  29.0
• 环数：
  7.0
• sp3杂化的碳原子比例：
  0.68
• 拓扑面积：
  364.06
• 氢给体数：
  3.0
• 氢受体数：
  28.0

反应信息

• 作为反应物：
  描述：

  6-chlorohexyl 2-acetamido-4-O-[2,4-di-O-acetyl-6-O-pivaloyl-3-O-(4,6-O-benzylidene-2-deoxy-2-trichloroacetamido-β-D-glucopyranosyl)-β-D-galactopyranosyl]-6-O-benzyl-3-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-2-deoxy-β-D-glucopyranoside 、 乙酸酐 以 吡啶 为溶剂， 反应 2.0h， 以100%的产率得到6-chlorohexyl 2-acetamido-4-O-[2,4-di-O-acetyl-6-O-pivaloyl-3-O-(4,6-O-benzylidene-3-O-acetyl-2-deoxy-2-trichloroacetamido-β-D-glucopyranosyl)-β-D-galactopyranosyl]-6-O-benzyl-3-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-2-deoxy-β-D-glucopyranoside
  参考文献：
  名称：

  Matched and mismatched acceptor/donor pairs in the glycosylation of a trisaccharide diol free at O-3 of two N-acylated glucosamine residues

  摘要：

  Reciprocal donor acceptor selectivity (RDAS) and double diastereodifferentiation are two concepts that have been used to explain how a glycosyl acceptor and donor may be 'matched' or 'mismatched' in glycosylation reactions. We describe here how the alpha-L-fucosylation and beta-D-galactosylation of a trisaccharide displaying two equatorial OH groups at C-3 of N-acylated glucosamine units led to different regioselectivities or different 'matched' pairs. These results may be explained under the reciprocal donor acceptor selectivity or double diastereodifferentiation concepts. We also suggest a third explanation to these results: the presence of a benzylidene at the nonreducing end acceptor led to rigidity at this residue which resulted into a mismatched pair during beta-D-galactosylation but allowed alpha-L-fucosylation. (C) 2012 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.carres.2012.04.020
• 作为产物：
  描述：

  6-chlorohexyl 2-acetamido-4-O-[2,4-di-O-acetyl-6-O-pivaloyl-3-O-(4,6-O-benzylidene-2-deoxy-2-trichloroacetamido-β-D-glucopyranosyl)-β-D-galactopyranosyl]-6-O-benzyl-2-deoxy-β-D-glucopyranoside 、 2,3,4,6-四乙酰氧基-alpha-D-吡喃糖溴化物 在 mercury(II) cyanide 作用下， 以 硝基甲烷 、 甲苯 为溶剂， 反应 5.0h， 以67%的产率得到6-chlorohexyl 2-acetamido-4-O-[2,4-di-O-acetyl-6-O-pivaloyl-3-O-(4,6-O-benzylidene-2-deoxy-2-trichloroacetamido-β-D-glucopyranosyl)-β-D-galactopyranosyl]-6-O-benzyl-3-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-2-deoxy-β-D-glucopyranoside
  参考文献：
  名称：

  Matched and mismatched acceptor/donor pairs in the glycosylation of a trisaccharide diol free at O-3 of two N-acylated glucosamine residues

  摘要：

  Reciprocal donor acceptor selectivity (RDAS) and double diastereodifferentiation are two concepts that have been used to explain how a glycosyl acceptor and donor may be 'matched' or 'mismatched' in glycosylation reactions. We describe here how the alpha-L-fucosylation and beta-D-galactosylation of a trisaccharide displaying two equatorial OH groups at C-3 of N-acylated glucosamine units led to different regioselectivities or different 'matched' pairs. These results may be explained under the reciprocal donor acceptor selectivity or double diastereodifferentiation concepts. We also suggest a third explanation to these results: the presence of a benzylidene at the nonreducing end acceptor led to rigidity at this residue which resulted into a mismatched pair during beta-D-galactosylation but allowed alpha-L-fucosylation. (C) 2012 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.carres.2012.04.020