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4-methoxyphenyl (methyl 7,8,9-tri-O-acetyl-5-N,4-O-carbonyl-3,5-dideoxy-D-glycero-α-D-galacto-non-2-ulopyranosylonate)-(2→6)-2,3,4-tri-O-benzyl-β-D-galacotopyranoside | 1415252-08-2

中文名称
——
中文别名
——
英文名称
4-methoxyphenyl (methyl 7,8,9-tri-O-acetyl-5-N,4-O-carbonyl-3,5-dideoxy-D-glycero-α-D-galacto-non-2-ulopyranosylonate)-(2→6)-2,3,4-tri-O-benzyl-β-D-galacotopyranoside
英文别名
methyl (3aR,4R,6R,7aS)-6-[[(2R,3S,4S,5R,6S)-6-(4-methoxyphenoxy)-3,4,5-tris(phenylmethoxy)oxan-2-yl]methoxy]-2-oxo-4-[(1S,2R)-1,2,3-triacetyloxypropyl]-3a,4,7,7a-tetrahydro-3H-pyrano[3,4-d][1,3]oxazole-6-carboxylate
4-methoxyphenyl (methyl 7,8,9-tri-O-acetyl-5-N,4-O-carbonyl-3,5-dideoxy-D-glycero-α-D-galacto-non-2-ulopyranosylonate)-(2→6)-2,3,4-tri-O-benzyl-β-D-galacotopyranoside化学式
CAS
1415252-08-2
化学式
C51H57NO18
mdl
——
分子量
972.009
InChiKey
LPWKBAIGCBXUJF-UFSXXFISSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    5.2
  • 重原子数:
    70
  • 可旋转键数:
    26
  • 环数:
    7.0
  • sp3杂化的碳原子比例:
    0.43
  • 拓扑面积:
    217
  • 氢给体数:
    1
  • 氢受体数:
    18

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    methyl (4S,5R,6R)-5-amino-4-hydroxy-2-(4-methylphenyl)sulfanyl-6-[(1R,2R)-1,2,3-trihydroxypropyl]oxane-2-carboxylate 在 吡啶N-碘代丁二酰亚胺三氟甲磺酸碳酸氢钠 作用下, 以 二氯甲烷乙腈 为溶剂, 反应 1.0h, 生成 4-methoxyphenyl (methyl 7,8,9-tri-O-acetyl-5-N,4-O-carbonyl-3,5-dideoxy-D-glycero-α-D-galacto-non-2-ulopyranosylonate)-(2→6)-2,3,4-tri-O-benzyl-β-D-galacotopyranoside
    参考文献:
    名称:
    Studies on the sialylation of galactoses with different C-5 modified sialyl donors
    摘要:
    Synthetic sialylated glycans provide useful tools to study carbohydrate-mediated biological recognition; however chemical sialylation is the most challenging practice in preparative carbohydrate chemistry, which is often associated with low yields and poor stereoselectivity. Herein, we conducted extensive studies on sialylation with five types of 5-N-modified sialyl donors and four types of galactosyl acceptors. Our studies have shown that a good combination between the donor and the acceptor seems necessary to achieve high yield and stereoselectivity. None of the donors or acceptors showed 'universal' utility toward the sialylation reaction. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.carres.2012.08.007
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