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1-[(2R,4S,5R)-4-[4-[[(2R,3S,5R)-3-hydroxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methyl]triazol-1-yl]-5-prop-2-ynyloxolan-2-yl]-5-methylpyrimidine-2,4-dione | 1173882-43-3

中文名称
——
中文别名
——
英文名称
1-[(2R,4S,5R)-4-[4-[[(2R,3S,5R)-3-hydroxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methyl]triazol-1-yl]-5-prop-2-ynyloxolan-2-yl]-5-methylpyrimidine-2,4-dione
英文别名
——
1-[(2R,4S,5R)-4-[4-[[(2R,3S,5R)-3-hydroxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methyl]triazol-1-yl]-5-prop-2-ynyloxolan-2-yl]-5-methylpyrimidine-2,4-dione化学式
CAS
1173882-43-3
化学式
C24H27N7O7
mdl
——
分子量
525.521
InChiKey
WLEBHLFLTFGJHC-VTYCOLDWSA-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):
    -0.9
  • 重原子数:
    38
  • 可旋转键数:
    6
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    168
  • 氢给体数:
    3
  • 氢受体数:
    9

反应信息

  • 作为反应物:
    描述:
    1-[(2R,4S,5R)-4-[4-[[(2R,3S,5R)-3-hydroxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methyl]triazol-1-yl]-5-prop-2-ynyloxolan-2-yl]-5-methylpyrimidine-2,4-dione 、 1-[(2R,4S,5R)-4-azido-5-[[1-[(2R,3S,5R)-5-(5-methyl-2,4-dioxopyrimidin-1-yl)-2-(3-trimethylsilylprop-2-ynyl)oxolan-3-yl]triazol-4-yl]methyl]oxolan-2-yl]-5-methylpyrimidine-2,4-dione 在 二甲基硫 作用下, 以 四氢呋喃叔丁醇 为溶剂, 反应 48.0h, 以95%的产率得到
    参考文献:
    名称:
    Convergent synthesis of oligomers of triazole-linked DNA analogue (TLDNA) in solution phase
    摘要:
    A convergent route for the solution-phase synthesis of oligomeric triazole-linked analogues of DNA ((TL)DNA) has been developed. A one-pot procedure for desilylation of masked acetylene and the ensuing copper-catalyzed Huisgen coupling reaction between oligomers allowed the solution-phase synthesis of 7-mer and 8-mer (TL)DNA in good yield. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2009.04.101
  • 作为产物:
    描述:
    1-((2R,4S,5R)-4-hydroxy-5-((1-((2R,3S,5R)-5-(5-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-2-(3-(trimethylsilyl)prop-2-yn-1-yl)tetrahydrofuran-3-yl)-1H-1,2,3-triazol-4-yl)methyl)tetrahydrofuran-2-yl)-5-methylpyrimidine-2,4(1H,3H)-dione 在 四丁基氟化铵 作用下, 以 四氢呋喃 为溶剂, 以96.8 mg的产率得到1-[(2R,4S,5R)-4-[4-[[(2R,3S,5R)-3-hydroxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methyl]triazol-1-yl]-5-prop-2-ynyloxolan-2-yl]-5-methylpyrimidine-2,4-dione
    参考文献:
    名称:
    Convergent synthesis of oligomers of triazole-linked DNA analogue (TLDNA) in solution phase
    摘要:
    A convergent route for the solution-phase synthesis of oligomeric triazole-linked analogues of DNA ((TL)DNA) has been developed. A one-pot procedure for desilylation of masked acetylene and the ensuing copper-catalyzed Huisgen coupling reaction between oligomers allowed the solution-phase synthesis of 7-mer and 8-mer (TL)DNA in good yield. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2009.04.101
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文献信息

  • Triazole-Linked Analogue of Deoxyribonucleic Acid (<sup>TL</sup>DNA): Design, Synthesis, and Double-Strand Formation with Natural DNA
    作者:Hiroyuki Isobe、Tomoko Fujino、Naomi Yamazaki、Marine Guillot-Nieckowski、Eiichi Nakamura
    DOI:10.1021/ol801230k
    日期:2008.9.1
    A new triazole-linked analogue of DNA ((TL)DNA) has been designed and synthesized using click chemistry. The chain elongation reaction using copper-catalyzed Huisgen cycloaddition was successful and gave the artificial oligonucleotide that formed a stable double strand with the complementary strand of natural DNA.
  • Convergent synthesis of oligomers of triazole-linked DNA analogue (TLDNA) in solution phase
    作者:Tomoko Fujino、Naomi Yamazaki、Hiroyuki Isobe
    DOI:10.1016/j.tetlet.2009.04.101
    日期:2009.7
    A convergent route for the solution-phase synthesis of oligomeric triazole-linked analogues of DNA ((TL)DNA) has been developed. A one-pot procedure for desilylation of masked acetylene and the ensuing copper-catalyzed Huisgen coupling reaction between oligomers allowed the solution-phase synthesis of 7-mer and 8-mer (TL)DNA in good yield. (C) 2009 Elsevier Ltd. All rights reserved.
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