1-adamantyl 3,4,6-tri-O-acetyl-2-amino-2-N-benzyloxycarbonyl-2-deoxy-α-D-mannopyranoside | 855271-08-8

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: 1-adamantyl 3,4,6-tri-O-acetyl-2-amino-2-N-benzyloxycarbonyl-2-deoxy-α-D-mannopyranoside
• 英文别名: [(2R,3S,4R,5S,6R)-3,4-diacetyloxy-6-(1-adamantyloxy)-5-(phenylmethoxycarbonylamino)oxan-2-yl]methyl acetate
• CAS: 855271-08-8
• 化学式: C₃₀H₃₉NO₁₀
• 分子量: 573.64
• InChiKey: ZVIGHCJSICJJTL-SQFLJABTSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.7
• 重原子数：
  41
• 可旋转键数：
  13
• 环数：
  6.0
• sp3杂化的碳原子比例：
  0.67
• 拓扑面积：
  136
• 氢给体数：
  1
• 氢受体数：
  10

反应信息

• 作为反应物：
  描述：

  1-adamantyl 3,4,6-tri-O-acetyl-2-amino-2-N-benzyloxycarbonyl-2-deoxy-α-D-mannopyranoside 在 palladium on activated charcoal 氢气 、 air 、 silica gel 作用下， 以 甲醇 、 乙酸乙酯 为溶剂， 23.0 ℃ 、101.32 kPa 条件下， 以82%的产率得到1-adamantyl 2-acetamido-4,6-di-O-acetyl-2-deoxy-α-D-mannopyranoside
  参考文献：
  名称：

  α-N-Acetylmannosamine (ManNAc) Synthesis via Rhodium(II)-Catalyzed Oxidative Cyclization of Glucal 3-Carbamates

  摘要：

  Glucal 3-carbamates 1 and 7 underwent oxidative cyclization with iodobenzene diacetate or iodosobenzene in the presence of Rh-2(OAc)(4), providing mannosamine 2-N,3-O-oxazolidinones. With iodosobenzene, incorporation of 4-penten-1-ol provided a readily separable anomeric mixture of n-pentenyl glycosides, with the anomers exhibiting pronounced differences in reactivity as glycosyl donors. N-acylation of the sugar oxazolidinones led to a-selective glycosyl donors for the elaboration of various 2-mannosamine frameworks. Alternatively, the anomeric n-pentenyl glycosides of N-Cbz 2-mannosamine oxazolidinones were converted separately to oxazolidinone-opened derivatives 28 alpha and 28 beta. These served as stereoconvergent glycosyl donors, and the a-linked products were readily advanced to a variety of N-acetylmannosamine (ManNAc) frameworks, using an intramolecular O -> N acetyl transfer as the final step.

  DOI：

  10.1021/jo0500129
• 作为产物：
  描述：

  4-pentenyl 2-amino-2-N,3-O-carbonyl-2-deoxy-4,6-O-isopropylidene-β-D-mannopyranoside 在 吡啶 、 4-二甲氨基吡啶 、 lithium hydroxide 、 N-碘代丁二酰亚胺 、 三乙基硅基三氟甲磺酸酯 、 三乙胺 作用下， 以 四氢呋喃 、 二氯甲烷 、 水 为溶剂， 反应 7.33h， 生成 1-adamantyl 3,4,6-tri-O-acetyl-2-amino-2-N-benzyloxycarbonyl-2-deoxy-α-D-mannopyranoside
  参考文献：
  名称：

  α-N-Acetylmannosamine (ManNAc) Synthesis via Rhodium(II)-Catalyzed Oxidative Cyclization of Glucal 3-Carbamates

  摘要：

  Glucal 3-carbamates 1 and 7 underwent oxidative cyclization with iodobenzene diacetate or iodosobenzene in the presence of Rh-2(OAc)(4), providing mannosamine 2-N,3-O-oxazolidinones. With iodosobenzene, incorporation of 4-penten-1-ol provided a readily separable anomeric mixture of n-pentenyl glycosides, with the anomers exhibiting pronounced differences in reactivity as glycosyl donors. N-acylation of the sugar oxazolidinones led to a-selective glycosyl donors for the elaboration of various 2-mannosamine frameworks. Alternatively, the anomeric n-pentenyl glycosides of N-Cbz 2-mannosamine oxazolidinones were converted separately to oxazolidinone-opened derivatives 28 alpha and 28 beta. These served as stereoconvergent glycosyl donors, and the a-linked products were readily advanced to a variety of N-acetylmannosamine (ManNAc) frameworks, using an intramolecular O -> N acetyl transfer as the final step.

  DOI：

  10.1021/jo0500129