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methyl 3,5-di-O-tert-butyldiphenylsilyl-2-O,4-C-methylene-D-ribofuranoside | 1029931-22-3

中文名称
——
中文别名
——
英文名称
methyl 3,5-di-O-tert-butyldiphenylsilyl-2-O,4-C-methylene-D-ribofuranoside
英文别名
——
methyl 3,5-di-O-tert-butyldiphenylsilyl-2-O,4-C-methylene-D-ribofuranoside化学式
CAS
1029931-22-3
化学式
C39H48O5Si2
mdl
——
分子量
652.978
InChiKey
QVBBHKOFMZKRDP-TXCFPHOOSA-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):
    5.65
  • 重原子数:
    46.0
  • 可旋转键数:
    10.0
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.38
  • 拓扑面积:
    46.15
  • 氢给体数:
    0.0
  • 氢受体数:
    5.0

反应信息

  • 作为反应物:
    描述:
    methyl 3,5-di-O-tert-butyldiphenylsilyl-2-O,4-C-methylene-D-ribofuranoside盐酸 作用下, 以 四氢呋喃 为溶剂, 反应 4.0h, 以96%的产率得到3,5-di-O-tert-butyldiphenylsilyl-2-O,4-C-methylene-D-ribofuranose
    参考文献:
    名称:
    Recognition of T·A interruption by 2′,4′-BNAs bearing heteroaromatic nucleobases through parallel motif triplex formation
    摘要:
    2'-O,4'-C-methylene bridged nucleic acid (2',4'-BNA) monomers bearing novel unnatural nucleobases, 4-(3-benzamidophenyl)-2-pyridone and 2-(N-methylbenzamido)thiazole, were synthesized and successfully incorporated into oligonucleotides. UV melting experiments showed that the corresponding oligonucleotide derivatives formed stable triplexes with dsDNA targets even in the presence of a T center dot A interruption. (C) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2007.12.043
  • 作为产物:
    描述:
    (1S,4R,7S)-1-(hydroxymethyl)-3-methoxy-2,5-dioxabicyclo[2.2.1]heptan-7-ol 、 叔丁基二苯基氯硅烷咪唑 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 12.0h, 以1.23 g的产率得到methyl 3,5-di-O-tert-butyldiphenylsilyl-2-O,4-C-methylene-D-ribofuranoside
    参考文献:
    名称:
    Recognition of T·A interruption by 2′,4′-BNAs bearing heteroaromatic nucleobases through parallel motif triplex formation
    摘要:
    2'-O,4'-C-methylene bridged nucleic acid (2',4'-BNA) monomers bearing novel unnatural nucleobases, 4-(3-benzamidophenyl)-2-pyridone and 2-(N-methylbenzamido)thiazole, were synthesized and successfully incorporated into oligonucleotides. UV melting experiments showed that the corresponding oligonucleotide derivatives formed stable triplexes with dsDNA targets even in the presence of a T center dot A interruption. (C) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2007.12.043
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