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4-methoxyphenyl (2-acetamido-2-deoxy-β-D-galactopyranosyl)-(1->3)-(β-D-galactopyranosyl)-(1->4)-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-(1->3)-(β-D-galactopyranosyl)-(1->4)-β-D-glucopyranoside | 1064679-28-2

中文名称
——
中文别名
——
英文名称
4-methoxyphenyl (2-acetamido-2-deoxy-β-D-galactopyranosyl)-(1->3)-(β-D-galactopyranosyl)-(1->4)-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-(1->3)-(β-D-galactopyranosyl)-(1->4)-β-D-glucopyranoside
英文别名
——
4-methoxyphenyl (2-acetamido-2-deoxy-β-D-galactopyranosyl)-(1->3)-(β-D-galactopyranosyl)-(1->4)-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-(1->3)-(β-D-galactopyranosyl)-(1->4)-β-D-glucopyranoside化学式
CAS
1064679-28-2
化学式
C41H64N2O27
mdl
——
分子量
1016.96
InChiKey
XYCHMNQJXXLDSW-MKDRGJLSSA-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

反应信息

  • 作为产物:
    描述:
    [(2R,3S,4S,5R,6S)-3-acetyloxy-6-[(2R,3S,4R,5R,6S)-6-[(2S,3R,4S,5S,6R)-5-acetyloxy-2-[(2R,3R,4S,5R,6S)-6-(4-methoxyphenoxy)-4,5-bis(phenylmethoxy)-2-(phenylmethoxymethyl)oxan-3-yl]oxy-3-phenylmethoxy-6-(phenylmethoxymethyl)oxan-4-yl]oxy-5-(1,3-dioxoisoindol-2-yl)-4-hydroxy-2-(phenylmethoxymethyl)oxan-3-yl]oxy-5-benzoyloxy-4-[(2S,3R,4R,5R,6R)-4,5-diacetyloxy-6-(acetyloxymethyl)-3-(1,3-dioxoisoindol-2-yl)oxan-2-yl]oxyoxan-2-yl]methyl benzoate 以70%的产率得到4-methoxyphenyl (2-acetamido-2-deoxy-β-D-galactopyranosyl)-(1->3)-(β-D-galactopyranosyl)-(1->4)-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-(1->3)-(β-D-galactopyranosyl)-(1->4)-β-D-glucopyranoside
    参考文献:
    名称:
    Concise synthesis of two pentasaccharides corresponding to the α-chain oligosaccharides of Neisseria gonorrhoeae and Neisseria meningitidis
    摘要:
    Two pentasaccharides containing a common tetrasaccharide (lacto-N-neotetraose) core, and D-galactosamine and N-acetyl neuraminic acid in the non-reducing ends, respectively, corresponding to the lipooligosaccharides of Neisseria gonorrhoeae and Neisseria meningitidis were synthesized in a very concise manner from a common trisaccharide derivative using minimum number of steps. Thioglycosides and glycosyl trichloroacetimidate have been used as glycosyl donors for glycosylations and yields were excellent in every step. (c) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2008.07.004
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