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1-((2R,4S,5R)-4-((tert-butyldiphenylsilyl)oxy)-5-ethynyltetrahydrofuran-2-yl)-5-methylpyrimidine-2,4(1H,3H)-dione | 1210349-14-6

中文名称
——
中文别名
——
英文名称
1-((2R,4S,5R)-4-((tert-butyldiphenylsilyl)oxy)-5-ethynyltetrahydrofuran-2-yl)-5-methylpyrimidine-2,4(1H,3H)-dione
英文别名
——
1-((2R,4S,5R)-4-((tert-butyldiphenylsilyl)oxy)-5-ethynyltetrahydrofuran-2-yl)-5-methylpyrimidine-2,4(1H,3H)-dione化学式
CAS
1210349-14-6
化学式
C27H30N2O4Si
mdl
——
分子量
474.632
InChiKey
IAOHJHWNIYJAMD-TZRRMPRUSA-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):
    2.71
  • 重原子数:
    34.0
  • 可旋转键数:
    5.0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    73.32
  • 氢给体数:
    1.0
  • 氢受体数:
    5.0

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

点击查看最新优质反应信息

文献信息

  • A One-Pot, Copper-Catalyzed Cascade Route to 2-Indolyl-C-glycosides
    作者:Parthasarathi Subramanian、Krishna P. Kaliappan
    DOI:10.1002/ejoc.201201208
    日期:2013.1
    An efficient and high-yielding, one-pot, Cu-catalyzed synthesis of 2-indolyl-C-glycosides is delineated. The sequence involves a cascade Sonogashira type coupling and a hydroamination reaction between sugar-derived alkynes and N-tosyl-o-iodoaniline followed by removal of the N-tosyl group to provide a library of 2-indolyl-C-glycosides in moderate to excellent yields.
    描述了一种高效且高产的单锅 Cu 催化合成 2-吲哚基-C-糖苷。该序列涉及级联 Sonogashira 型偶联和糖衍生的炔烃和 N-甲苯磺酰基-邻苯胺之间的加氢胺化反应,然后去除 N-甲苯磺酰基,以提供中等至优异的 2-吲哚基-C-糖苷库产量。
  • Synthesis of Triazole-Linked Oligonucleotides with High Affinity to DNA Complements and an Analysis of Their Compatibility with Biosystems
    作者:Anna M. Varizhuk、Dmitry N. Kaluzhny、Roman A. Novikov、Alexandr O. Chizhov、Igor P. Smirnov、Andrey N. Chuvilin、Olga N. Tatarinova、Gleb Y. Fisunov、Galina E. Pozmogova、Vladimir L. Florentiev
    DOI:10.1021/jo400651k
    日期:2013.6.21
    New oligonucleotide analogues with triazole internucleotide linkages were synthesized, and their hybridization properties were studied. The analogues demonstrated DNA binding affinities similar to those of unmodified oligonucleotides. The modification was shown to protect the oligonucleotides from nuclease hydrolysis. The modified oligonucleotides were tested as PCR primers. Modifications remote from the 3'-terminus were tolerated by polymerases. Our results suggest that these new oligonucleotide analogues are among the most promising triazole DNA mimics characterized to date.
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