O-β-D-galctopyranosyl-(1->2)-α-D-glucopyranosyl-α-D-glucopyranoside | 129261-47-8

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: O-β-D-galctopyranosyl-(1->2)-α-D-glucopyranosyl-α-D-glucopyranoside
• 英文别名: Gal(b1-2)Glc(a1-1a)Glc；(2S,3R,4S,5R,6R)-2-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol
• CAS: 129261-47-8
• 化学式: C₁₈H₃₂O₁₆
• 分子量: 504.442
• InChiKey: ZZQBFMYCMRVZFG-SWANJTMFSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -5.8
• 重原子数：
  34
• 可旋转键数：
  7
• 环数：
  3.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  269
• 氢给体数：
  11
• 氢受体数：
  16

反应信息

• 作为反应物：
  描述：

  乙酸酐 、 O-β-D-galctopyranosyl-(1->2)-α-D-glucopyranosyl-α-D-glucopyranoside 在 吡啶 作用下， 生成 2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl-(1->6)-2,3,4-tri-O-acetyl-α-D-glucopyranosyl 2,3,4,6-tetra-O-acetyl-α-D-glucopyranoside 、 2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl-(1->4)-2,3,6-tri-O-acetyl-α-D-glucopyranosyl 2,3,4,6-tetra-O-acetyl-α-D-glucopyranoside 、 2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl-(1->2)-3,4,6-tri-O-acetyl-α-D-glucopyranosyl 2,3,4,6-tetra-O-acetyl-α-D-glucopyranoside 、 2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl-(1->3)-2,4,6-tri-O-acetyl-α-D-glucopyranosyl 2,3,4,6-tetra-O-acetyl-α-D-glucopyranoside
  参考文献：
  名称：

  未受保护的非还原性单糖和双糖的首次直接糖基化

  摘要：

  完全无保护的糖基受体的第一个单步随机糖基化方法报告通过随机糖基化导致所有可能的区域异构体。对于此类系统，传统的糖基化方法，例如 Koenigs-Knorr 糖基化、Schmidt 的三氯乙酰亚胺糖基化和使用糖基氟供体的反应完全失败。从未受保护的非还原糖开始，研究了 β-葡萄糖基化和 β-半乳糖基化单糖（Glc、Gal）、对称二糖（例如 α,α-海藻糖）以及不对称二糖（例如蔗糖）的糖基化。检查了碱类型和浓度的影响。生成了几个二糖和三糖文库。所有区域异构体以大致相等的比例形成，用快速柱色谱法实现部分分离。尽管与经典的保护基化学相比，总体产率似乎较低，但这种合成努力可能更胜一筹，尤其是在获得更高的糖类方面。(© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007)

  DOI：

  10.1002/ejoc.200700504
• 作为产物：
  描述：

  海藻糖 、 口服葡萄糖 在 phosphate buffer 、 β-galactosidase 作用下， 反应 22.0h， 生成 O-β-D-galctopyranosyl-(1->2)-α-D-glucopyranosyl-α-D-glucopyranoside 、 O-β-D-galctopyranosyl-(1->3)-α-D-glucopyranosyl-α-D-glucopyranoside 、 O-β-D-galctopyranosyl-(1->4)-α-D-glucopyranosyl-α-D-glucopyranoside 、 O-β-D-galctopyranosyl-(1->6)-α-D-glucopyranosyl-α-D-glucopyranoside
  参考文献：
  名称：

  Regioselective syntheses of trehalose-containing trisaccharides using various glycohydrolases

  摘要：

  Two methods were investigated for the enzymic preparation of trehalose-containing trisaccharides. In the first, a solution of saccharides is circulated through an immobilized-glycosidase column and an activated-carbon column connected in series. In the second, two enzymes having different substrate specificities are sequentially used for condensation and subsequent specific hydrolysis. Thus, 3-O-beta-D-, 4-O-beta-D-, and 6-O-beta-D-galactopyranosyl-alpha,alpha-trehalose; 4-O-alpha-D- and 6-O-alpha-D-glucopyranosyl-alpha,alpha-trehalose; and 4-O-beta-D- and 6-O-beta-D-glucopyranosyl-alpha,alpha-trehalose were synthesized stereo- and regio-selectively.

  DOI：

  10.1016/0008-6215(90)84264-u

文献信息

• First Direct Glycosylation of Unprotected Nonreducing Mono- and Disaccharides
  作者：Andreas Steinmann、Julian Thimm、Joachim Thiem

  DOI：10.1002/ejoc.200700504

  日期：2007.11

  glycosyl acceptors is reported by random glycosylation leading to all possible regioisomers. For such systems conventional glycosylation methods such as Koenigs–Knorr glycosylation, Schmidt's trichloroacetimidate glycosylation and reactions employing glycosyl fluoride donors fail entirely. Starting from unprotected nonreducing saccharides, the glycosylation of β-glucosylated and β-galactosylated monosaccharides

  完全无保护的糖基受体的第一个单步随机糖基化方法报告通过随机糖基化导致所有可能的区域异构体。对于此类系统，传统的糖基化方法，例如 Koenigs-Knorr 糖基化、Schmidt 的三氯乙酰亚胺糖基化和使用糖基氟供体的反应完全失败。从未受保护的非还原糖开始，研究了 β-葡萄糖基化和 β-半乳糖基化单糖（Glc、Gal）、对称二糖（例如 α,α-海藻糖）以及不对称二糖（例如蔗糖）的糖基化。检查了碱类型和浓度的影响。生成了几个二糖和三糖文库。所有区域异构体以大致相等的比例形成，用快速柱色谱法实现部分分离。尽管与经典的保护基化学相比，总体产率似乎较低，但这种合成努力可能更胜一筹，尤其是在获得更高的糖类方面。(© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007)
• Regioselective syntheses of trehalose-containing trisaccharides using various glycohydrolases
  作者：Katsumi Ajisaka、Hiroshi Fujimoto

  DOI：10.1016/0008-6215(90)84264-u

  日期：1990.6

  Two methods were investigated for the enzymic preparation of trehalose-containing trisaccharides. In the first, a solution of saccharides is circulated through an immobilized-glycosidase column and an activated-carbon column connected in series. In the second, two enzymes having different substrate specificities are sequentially used for condensation and subsequent specific hydrolysis. Thus, 3-O-beta-D-, 4-O-beta-D-, and 6-O-beta-D-galactopyranosyl-alpha,alpha-trehalose; 4-O-alpha-D- and 6-O-alpha-D-glucopyranosyl-alpha,alpha-trehalose; and 4-O-beta-D- and 6-O-beta-D-glucopyranosyl-alpha,alpha-trehalose were synthesized stereo- and regio-selectively.