allyl O-(4-O-acetyl-2,3-di-O-methyl-α-L-fucopyranosyl)-(1->3)-2,4-di-O-benzoyl-α-L-rhamnopyranoside | 136737-76-3

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: allyl O-(4-O-acetyl-2,3-di-O-methyl-α-L-fucopyranosyl)-(1->3)-2,4-di-O-benzoyl-α-L-rhamnopyranoside
• CAS: 136737-76-3
• 化学式: C₃₃H₄₀O₁₂
• 分子量: 628.673
• InChiKey: AZFLHSSFAYDGJW-CKXXNJRCSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.48
• 重原子数：
  45.0
• 可旋转键数：
  12.0
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.48
• 拓扑面积：
  134.28
• 氢给体数：
  0.0
• 氢受体数：
  12.0

反应信息

• 作为反应物：
  描述：

  allyl O-(4-O-acetyl-2,3-di-O-methyl-α-L-fucopyranosyl)-(1->3)-2,4-di-O-benzoyl-α-L-rhamnopyranoside 在 sodium methylate 作用下， 以 甲醇 为溶剂， 以88%的产率得到allyl O-(2,3-di-O-methyl-α-L-fucopyranosyl)-(1->3)-α-L-rhamnopyranoside
  参考文献：
  名称：

  Synthesis of allyl glycosides for conversion into neoglycoproteins bearing epitopes of mycobacterial glycolipid antigens

  摘要：

  Neoglycoproteins bearing key glycosyl substituents of several glycopeptidolipid antigens of pathogenic Mycobacterium species have been synthesized. Allyl glycosides of the terminal 6-deoxyhexose-containing units of the antigens were prepared, with appropriate ether and ester substituents in place. Ozonolysis of the allyl glycosides was then followed by reductive coupling with epsilon-amino groups of lysine residues in bovine serum albumin, using sodium cyanoborohydride at pH 7.8. The resulting neoglycoproteins emulated the antigenicity of the native molecule in several serological tests.

  DOI：

  10.1016/0008-6215(92)84172-o
• 作为产物：
  描述：

  allyl 2,3-di-O-methyl-α-L-fucopyranoside 在 1,8-二氮杂双环[5.4.0]十一碳-7-烯 吡啶 、 selenium(IV) oxide 、 4 A molecular sieve 、 三氟化硼乙醚 、 溶剂黄146 作用下， 以 1,4-二氧六环 、 二氯甲烷 为溶剂， 反应 2.5h， 生成 allyl O-(4-O-acetyl-2,3-di-O-methyl-α-L-fucopyranosyl)-(1->3)-2,4-di-O-benzoyl-α-L-rhamnopyranoside
  参考文献：
  名称：

  Synthesis of allyl glycosides for conversion into neoglycoproteins bearing epitopes of mycobacterial glycolipid antigens

  摘要：

  Neoglycoproteins bearing key glycosyl substituents of several glycopeptidolipid antigens of pathogenic Mycobacterium species have been synthesized. Allyl glycosides of the terminal 6-deoxyhexose-containing units of the antigens were prepared, with appropriate ether and ester substituents in place. Ozonolysis of the allyl glycosides was then followed by reductive coupling with epsilon-amino groups of lysine residues in bovine serum albumin, using sodium cyanoborohydride at pH 7.8. The resulting neoglycoproteins emulated the antigenicity of the native molecule in several serological tests.

  DOI：

  10.1016/0008-6215(92)84172-o