2,3,4-tri-O-benzoyl-N-(2,2-diethoxycarbonylvinyl)-6-O-trityl-β-D-galactopyranosylamine | 488827-77-6

• 分子结构分类: 有机化合物 - 苯类化合物 - 三苯基化合物
• 英文名称: 2,3,4-tri-O-benzoyl-N-(2,2-diethoxycarbonylvinyl)-6-O-trityl-β-D-galactopyranosylamine
• 英文别名: diethyl 2-[[[(2R,3R,4S,5S,6R)-3,4,5-tribenzoyloxy-6-(trityloxymethyl)oxan-2-yl]amino]methylidene]propanedioate
• CAS: 488827-77-6
• 化学式: C₅₄H₄₉NO₁₂
• 分子量: 903.983
• InChiKey: DLBSJWLKULFHCN-SSWAHCEOSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  10.9
• 重原子数：
  67
• 可旋转键数：
  23
• 环数：
  7.0
• sp3杂化的碳原子比例：
  0.2
• 拓扑面积：
  162
• 氢给体数：
  1
• 氢受体数：
  13

反应信息

• 作为反应物：
  描述：

  2,3,4-tri-O-benzoyl-N-(2,2-diethoxycarbonylvinyl)-6-O-trityl-β-D-galactopyranosylamine 在 三氟乙酸 作用下， 反应 0.08h， 以83%的产率得到2,3,4-tri-O-benzoyl-N-(2,2-diethoxycarbonylvinyl)-β-D-galactopyranosylamine
  参考文献：
  名称：

  An easy route to seven-membered iminocyclitols from aldohexopyranosyl enamines

  摘要：

  A new stereocontrolled and high yielding synthesis of biologically active polyhydroxyperhydroazelpines is reported starting from easily available glycosylenamines (D-gluco, D-manno, and D-galacto configurations), which are transformed into 1,6-azaanhydropyranose derivatives. O- and N-Deprotection of the latter, followed by reduction with sodium cyanoborohydride, gives the target chiral iminocyclitols. The method is based on the capacity of the dialkoxycarbonylvinyl group to stabilize an amide ion, and the only limitation is the necessity for the starting glycosylenamine to have beta-D-configuration. The inhibitory activity of several intermediate iminocyclitols and aldopyranosylenamines on different alpha- and beta-glycosidases is also reported. (C) 2002 Published by Elsevier Science Ltd.

  DOI：

  10.1016/s0957-4166(02)00377-4
• 作为产物：
  描述：

  N-(2,2-diethoxycarbonylvinyl)-β-D-galactopyranosylamine 在 吡啶 作用下， 反应 48.0h， 生成 2,3,4-tri-O-benzoyl-N-(2,2-diethoxycarbonylvinyl)-6-O-trityl-β-D-galactopyranosylamine
  参考文献：
  名称：

  An easy route to seven-membered iminocyclitols from aldohexopyranosyl enamines

  摘要：

  A new stereocontrolled and high yielding synthesis of biologically active polyhydroxyperhydroazelpines is reported starting from easily available glycosylenamines (D-gluco, D-manno, and D-galacto configurations), which are transformed into 1,6-azaanhydropyranose derivatives. O- and N-Deprotection of the latter, followed by reduction with sodium cyanoborohydride, gives the target chiral iminocyclitols. The method is based on the capacity of the dialkoxycarbonylvinyl group to stabilize an amide ion, and the only limitation is the necessity for the starting glycosylenamine to have beta-D-configuration. The inhibitory activity of several intermediate iminocyclitols and aldopyranosylenamines on different alpha- and beta-glycosidases is also reported. (C) 2002 Published by Elsevier Science Ltd.

  DOI：

  10.1016/s0957-4166(02)00377-4