tert-butyldiphenylsilyl O-(6-O-acetyl-2,3-di-O-benzyl-α-D-galactopyranosyl)-<(1->4)-O-(6-O-acetyl-2,3-di-O-benzyl-α-D-galactopyranosyl)>₄-(1->4)-6-O-acetyl-2,3-di-O-benzyl-β-D-galactopyranoside | 131219-85-7

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: tert-butyldiphenylsilyl O-(6-O-acetyl-2,3-di-O-benzyl-α-D-galactopyranosyl)-<(1->4)-O-(6-O-acetyl-2,3-di-O-benzyl-α-D-galactopyranosyl)>₄-(1->4)-6-O-acetyl-2,3-di-O-benzyl-β-D-galactopyranoside
• CAS: 131219-85-7
• 化学式: C₁₄₈H₁₆₄O₃₇Si
• 分子量: 2562.99
• InChiKey: DXKSWBZERMYUFW-JIUCHRCJSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  19.6
• 重原子数：
  186
• 可旋转键数：
  69
• 环数：
  20.0
• sp3杂化的碳原子比例：
  0.39
• 拓扑面积：
  400
• 氢给体数：
  1
• 氢受体数：
  37

反应信息

• 作为反应物：
  描述：

  O-(2,3-di-O-benzyl-4,6-O-isopropylidene-α-D-galactopyranosyl)-(1->4)-6-O-acetyl-2,3-di-O-benzyl-D-galactopyranosyl fluoride 、 tert-butyldiphenylsilyl O-(6-O-acetyl-2,3-di-O-benzyl-α-D-galactopyranosyl)-<(1->4)-O-(6-O-acetyl-2,3-di-O-benzyl-α-D-galactopyranosyl)>₄-(1->4)-6-O-acetyl-2,3-di-O-benzyl-β-D-galactopyranoside 、 O-(6-O-acetyl-2,3,4-tri-O-benzyl-α-D-galactopyranosyl)-<(1->4)-O-(6-O-acetyl-2,3-di-O-benzyl-α-D-galactopyranosyl)>₂-(1->4)-6-O-acetyl-2,3-di-O-benzyl-D-galactopyranosyl fluoride 生成 O-(α-D-galactopyranosyluronic acid)-<(1->4)-O-(α-D-galactopyranosyluronic acid)>₁₀-(1->4)-D-galactopyranuronic acid
  参考文献：
  名称：

  Stereoselective total synthesis of dodecagalacturonic acid, a phytoalexin elicitor of soybean

  摘要：

  O-(alpha-D-Galactopyranosyluronic acid)-[(1----4)-O-(alpha-D-galactopyranosyluronic acid)]10-D-galactopyranuronic acid (1), an endogenous elicitor of the phytoalexin of soybean, was synthesized by way of highly stereoselective glycosylations that involved glycosyl fluorides as the donors and oxidation of the twelve primary hydroxyl groups in the alpha-(1----4)-linked galactododecaoside derivative.

  DOI：

  10.1016/0008-6215(90)80135-p
• 作为产物：
  描述：

  tert-butyldiphenylsilyl O-(2,3-di-O-benzyl-α-D-galactopyranosyl)-<(1->4)-O-(6-O-acetyl-2,3-di-O-benzyl-α-D-galactopyranosyl)>₄-(1->4)-6-O-acetyl-2,3-di-O-benzyl-β-D-galactopyranoside 、 乙酰氯 在 吡啶 作用下， 反应 5.0h， 以83.4%的产率得到tert-butyldiphenylsilyl O-(6-O-acetyl-2,3-di-O-benzyl-α-D-galactopyranosyl)-<(1->4)-O-(6-O-acetyl-2,3-di-O-benzyl-α-D-galactopyranosyl)>₄-(1->4)-6-O-acetyl-2,3-di-O-benzyl-β-D-galactopyranoside
  参考文献：
  名称：

  Stereoselective total synthesis of dodecagalacturonic acid, a phytoalexin elicitor of soybean

  摘要：

  O-(alpha-D-Galactopyranosyluronic acid)-[(1----4)-O-(alpha-D-galactopyranosyluronic acid)]10-D-galactopyranuronic acid (1), an endogenous elicitor of the phytoalexin of soybean, was synthesized by way of highly stereoselective glycosylations that involved glycosyl fluorides as the donors and oxidation of the twelve primary hydroxyl groups in the alpha-(1----4)-linked galactododecaoside derivative.

  DOI：

  10.1016/0008-6215(90)80135-p

文献信息

• NAKAHARA, YOSHIAKI;OGAWA, TOMOYA, CARBOHYDR. RES., 205,(1990) C. 147-159
  作者：NAKAHARA, YOSHIAKI、OGAWA, TOMOYA

  DOI：——

  日期：——