methyl 2-acetamido-4,6-di-O-acetyl-2,3-N,O-carbonyl-2-deoxy-α-D-glucopyranosyl-(1-3)-2,4,6-tri-O-benzyl-β-D-galactopyranoside | 1057668-84-4

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: methyl 2-acetamido-4,6-di-O-acetyl-2,3-N,O-carbonyl-2-deoxy-α-D-glucopyranosyl-(1-3)-2,4,6-tri-O-benzyl-β-D-galactopyranoside
• 英文别名: [(3aR,4R,6R,7S,7aR)-3-acetyl-7-acetyloxy-4-[(2R,3R,4S,5S,6R)-2-methoxy-3,5-bis(phenylmethoxy)-6-(phenylmethoxymethyl)oxan-4-yl]oxy-2-oxo-4,6,7,7a-tetrahydro-3aH-pyrano[3,4-d][1,3]oxazol-6-yl]methyl acetate
• CAS: 1057668-84-4
• 化学式: C₄₁H₄₇NO₁₄
• 分子量: 777.822
• InChiKey: IEHHSIAVVSDWTP-QCISSENZSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.3
• 重原子数：
  56
• 可旋转键数：
  18
• 环数：
  6.0
• sp3杂化的碳原子比例：
  0.46
• 拓扑面积：
  164
• 氢给体数：
  0
• 氢受体数：
  14

反应信息

• 作为产物：
  描述：

  ethyl 2-acetamido-4,6-di-O-acetyl-2,3-N,O-carbonyl-2-deoxy-1-thio-β-D-glucopyranoside 、 methyl 2,4,6-tri-O-benzyl-β-D-galactopyranoside 在 N-碘代丁二酰亚胺 、 silver trifluoroacetate 作用下， 以 二氯甲烷 为溶剂， 以82%的产率得到methyl 2-acetamido-4,6-di-O-acetyl-2,3-N,O-carbonyl-2-deoxy-α-D-glucopyranosyl-(1-3)-2,4,6-tri-O-benzyl-β-D-galactopyranoside
  参考文献：
  名称：

  Investigations of Glycosylation Reactions with 2-N-Acetyl-2N,3O-oxazolidinone-Protected Glucosamine Donors

  摘要：

  NIS/AgOTf-promoted glycosylations with ethyl 2,3-N,O-carbonyl-2-deoxy-1-thio-beta-D-glueopyranoside donors can be performed with either alpha- or beta-selectivity by tuning the reaction conditions. Small amounts of AgOTf (0.1 equiv) and short reaction times give beta-selectivity, whereas 0.4 equiv of AgOTf and prolonged reaction times afford alpha-linked products. NMR-monitored glycosylation and anomerization experiments show initial formation of exclusively the beta-linkage, which anomerizes, through an intramolecular mechanism involving an endocyclic C - O bond cleavage, to the alpha-linkage.

  DOI：

  10.1021/jo800971s