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4,5-di(methoxycarbonyl)-1-(ethyl 6-O-tert-butyldimethylsilyl-2,3,4-trideoxy-α-D-erythro-hex-2-enopyranosid-4-yl)-1H-1,2,3-triazole | 914795-44-1

中文名称
——
中文别名
——
英文名称
4,5-di(methoxycarbonyl)-1-(ethyl 6-O-tert-butyldimethylsilyl-2,3,4-trideoxy-α-D-erythro-hex-2-enopyranosid-4-yl)-1H-1,2,3-triazole
英文别名
dimethyl 1-[(2S,3S,6S)-2-[[tert-butyl(dimethyl)silyl]oxymethyl]-6-ethoxy-3,6-dihydro-2H-pyran-3-yl]triazole-4,5-dicarboxylate
4,5-di(methoxycarbonyl)-1-(ethyl 6-O-tert-butyldimethylsilyl-2,3,4-trideoxy-α-D-erythro-hex-2-enopyranosid-4-yl)-1H-1,2,3-triazole化学式
CAS
914795-44-1
化学式
C20H33N3O7Si
mdl
——
分子量
455.583
InChiKey
QHUSSJICKYQNFP-ZNMIVQPWSA-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):
    2.73
  • 重原子数:
    31
  • 可旋转键数:
    11
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.7
  • 拓扑面积:
    111
  • 氢给体数:
    0
  • 氢受体数:
    9

反应信息

  • 作为反应物:
    描述:
    4,5-di(methoxycarbonyl)-1-(ethyl 6-O-tert-butyldimethylsilyl-2,3,4-trideoxy-α-D-erythro-hex-2-enopyranosid-4-yl)-1H-1,2,3-triazole吡啶四氧化锇N-甲基吗啉氧化物 作用下, 以 丙酮 为溶剂, 生成 4,5-di(methoxycarbonyl)-1-(ethyl 2,3-di-O-acetyl-4-deoxy-6-O-tert-butyldimethylsilyl-α-D-mannopyranosid-4-yl)-1H-1,2,3-triazole
    参考文献:
    名称:
    Efficient Synthesis of Some Unsaturated [1,2,3]‐Triazole‐Linked Glycoconjugates
    摘要:
    Thermal 1,3-dipolar cycloaddition of ethyl 4-azido-2,3,4-trideoxy-alpha-D- erythro -hex-2-enopyranosides with diethyl acetylenedicarboxylate or copper-catalyzed reaction with various functionalized alkynes gave the corresponding 1-(ethyl 2,3,4-trideoxy-alpha-D- erythro -hex-2-enopyranosid-4-yl)-1 H -1,2,3-triazole derivatives in quite good yields. These unsaturated compounds could be transformed into 1-(ethyl 2,3-di-O-acetyl-4-deoxy-alpha-D-mannopyranosid-4-yl)-1 H -1,2,3-triazoles by a simple dihydroxylation reaction. Copper-catalyzed condensation of ethyl 6-O-acetyl-4-azido-2,3,4-trideoxy-alpha-D- erythro-hex-2-enopyranoside with 1,3,5-triethynylbenzene or 1,3,5-tris(prop-2-ynyloxy)benzene afforded the corresponding trivalent glycoconjugate clusters.
    DOI:
    10.1080/07328300600803484
  • 作为产物:
    参考文献:
    名称:
    Efficient Synthesis of Some Unsaturated [1,2,3]‐Triazole‐Linked Glycoconjugates
    摘要:
    Thermal 1,3-dipolar cycloaddition of ethyl 4-azido-2,3,4-trideoxy-alpha-D- erythro -hex-2-enopyranosides with diethyl acetylenedicarboxylate or copper-catalyzed reaction with various functionalized alkynes gave the corresponding 1-(ethyl 2,3,4-trideoxy-alpha-D- erythro -hex-2-enopyranosid-4-yl)-1 H -1,2,3-triazole derivatives in quite good yields. These unsaturated compounds could be transformed into 1-(ethyl 2,3-di-O-acetyl-4-deoxy-alpha-D-mannopyranosid-4-yl)-1 H -1,2,3-triazoles by a simple dihydroxylation reaction. Copper-catalyzed condensation of ethyl 6-O-acetyl-4-azido-2,3,4-trideoxy-alpha-D- erythro-hex-2-enopyranoside with 1,3,5-triethynylbenzene or 1,3,5-tris(prop-2-ynyloxy)benzene afforded the corresponding trivalent glycoconjugate clusters.
    DOI:
    10.1080/07328300600803484
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文献信息

  • Efficient Synthesis of Some Unsaturated [1,2,3]‐Triazole‐Linked Glycoconjugates
    作者:Ronaldo N. de Oliveira、Denis Sinou、Rajendra M. Srivastava
    DOI:10.1080/07328300600803484
    日期:2006.7
    Thermal 1,3-dipolar cycloaddition of ethyl 4-azido-2,3,4-trideoxy-alpha-D- erythro -hex-2-enopyranosides with diethyl acetylenedicarboxylate or copper-catalyzed reaction with various functionalized alkynes gave the corresponding 1-(ethyl 2,3,4-trideoxy-alpha-D- erythro -hex-2-enopyranosid-4-yl)-1 H -1,2,3-triazole derivatives in quite good yields. These unsaturated compounds could be transformed into 1-(ethyl 2,3-di-O-acetyl-4-deoxy-alpha-D-mannopyranosid-4-yl)-1 H -1,2,3-triazoles by a simple dihydroxylation reaction. Copper-catalyzed condensation of ethyl 6-O-acetyl-4-azido-2,3,4-trideoxy-alpha-D- erythro-hex-2-enopyranoside with 1,3,5-triethynylbenzene or 1,3,5-tris(prop-2-ynyloxy)benzene afforded the corresponding trivalent glycoconjugate clusters.
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