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(2R,3R,4S,5R,6S)-2-((4-(hydroxy(phenyl)methyl)-1H-1,2,3-triazol-1-yl)methyl)-6-methoxy-5-(tosyloxy)tetrahydro-2H-pyran-3,4-diyl dibenzoate | 1063719-71-0

中文名称
——
中文别名
——
英文名称
(2R,3R,4S,5R,6S)-2-((4-(hydroxy(phenyl)methyl)-1H-1,2,3-triazol-1-yl)methyl)-6-methoxy-5-(tosyloxy)tetrahydro-2H-pyran-3,4-diyl dibenzoate
英文别名
——
(2R,3R,4S,5R,6S)-2-((4-(hydroxy(phenyl)methyl)-1H-1,2,3-triazol-1-yl)methyl)-6-methoxy-5-(tosyloxy)tetrahydro-2H-pyran-3,4-diyl dibenzoate化学式
CAS
1063719-71-0
化学式
C37H35N3O10S
mdl
——
分子量
713.765
InChiKey
BOAOENZYFNTKAV-HHNYDIIMSA-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):
    4.26
  • 重原子数:
    51.0
  • 可旋转键数:
    12.0
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.24
  • 拓扑面积:
    165.37
  • 氢给体数:
    1.0
  • 氢受体数:
    13.0

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 3,4-di-O-benzoyl-6-deoxy-6-azido-2-O-tosyl-α-D-glucopyranoside(+/-)-1-苯基-2-丙炔-1-醇 在 Cu(I)-modified zeolite 作用下, 以 甲苯 为溶剂, 反应 8.0h, 以94%的产率得到(2R,3R,4S,5R,6S)-2-((4-(hydroxy(phenyl)methyl)-1H-1,2,3-triazol-1-yl)methyl)-6-methoxy-5-(tosyloxy)tetrahydro-2H-pyran-3,4-diyl dibenzoate
    参考文献:
    名称:
    ‘Click chemistry’ in CuI-zeolites: a convenient access to glycoconjugates
    摘要:
    Zeolites modified with Cu-I ions are efficient catalyst for 'click' reactions involving carbohydrates and aminoacid derivatives. Glycopeptides and oligosaccharides mimics as well as multivalent carbohydrate derivatives have been obtained in good to high yield using heterogeneous Cu-I-modified zeolite catalysts. Contrarily to expectation, pore sizes and internal shapes within zeolites were not a limitation and large glucosyl ditriazoles, disaccharide triazoles, and glucosylated triazolylaminoacids could easily be obtained. Such Cu-I-zeolite heterogeneous catalysts greatly facilitated products recovery, through an easy filtration-solvent evaporation sequence, thus offering a convenient alternative to current methods. (C) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2008.06.086
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