3-amino-3-deoxy-α-D-glucopyranosyl-(1→1')-β-D-glucopyranoside | 1417807-39-6

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 3-amino-3-deoxy-α-D-glucopyranosyl-(1→1')-β-D-glucopyranoside
• 英文别名: Glc3N(a1-1b)Glc；(2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5S,6R)-4-amino-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol
• CAS: 1417807-39-6
• 化学式: C₁₂H₂₃NO₁₀
• 分子量: 341.315
• InChiKey: OHNBYBTUSOVUMK-FPIKPGRSSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -4.4
• 重原子数：
  23
• 可旋转键数：
  4
• 环数：
  2.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  195
• 氢给体数：
  8
• 氢受体数：
  11

反应信息

• 作为产物：
  描述：

  2,4,6-tri-O-acetyl-3-azido-3-deoxy-α-D-glucopyranosyl-(1→1')-2',3',4',6'-tetra-O-acetyl-β-D-glucopyranoside 在 palladium on activated charcoal 、 氢气 、 sodium methylate 作用下， 以 甲醇 为溶剂， 反应 48.0h， 生成 3-amino-3-deoxy-α-D-glucopyranosyl-(1→1')-β-D-glucopyranoside
  参考文献：
  名称：

  Synthesis of 3,3′-neotrehalosadiamine and related 1,1′-aminodisaccharides using disarmed, armed, and superarmed building blocks

  摘要：

  Here we report a high yielding, stereoselective synthesis of the naturally occurring 1,1'-disaccharide neotrehalosadiamine (NTD) and some related analogs. Following an eleven-step sequence, seven of which did not require chromatographic separation, NTD was generated in 60% overall yield from the inexpensive, commercially available precursor 1,2:5,6-di-O-isopropylidene-alpha-D-glucofuranose. The key alpha,beta-linkage of NTD was formed in a highly stereoselective manner by taking advantage of the participating effect of the acyl group at O-2 of the donor glycoside. The influence of electronic effects of disarmed, armed, and superarmed glycosyl donors and acceptors on the outcome of 1,1'-glycosidation was also observed. Antibacterial studies using NTD and its analogs show detectable but weak antistaphylococcal activity. (c) 2012 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2012.10.058

文献信息

• Synthesis of 3,3′-neotrehalosadiamine and related 1,1′-aminodisaccharides using disarmed, armed, and superarmed building blocks
  作者：Shazia Anjum、Natasha D. Vetter、Joseph E. Rubin、David R.J. Palmer

  DOI：10.1016/j.tet.2012.10.058

  日期：2013.1

  Here we report a high yielding, stereoselective synthesis of the naturally occurring 1,1'-disaccharide neotrehalosadiamine (NTD) and some related analogs. Following an eleven-step sequence, seven of which did not require chromatographic separation, NTD was generated in 60% overall yield from the inexpensive, commercially available precursor 1,2:5,6-di-O-isopropylidene-alpha-D-glucofuranose. The key alpha,beta-linkage of NTD was formed in a highly stereoselective manner by taking advantage of the participating effect of the acyl group at O-2 of the donor glycoside. The influence of electronic effects of disarmed, armed, and superarmed glycosyl donors and acceptors on the outcome of 1,1'-glycosidation was also observed. Antibacterial studies using NTD and its analogs show detectable but weak antistaphylococcal activity. (c) 2012 Elsevier Ltd. All rights reserved.