N2,O6,O3',O5'-tetrakis-trimethylsilanyl-2'-deoxy-guanosine | 123389-63-9

• 分子结构分类: 有机化合物 - 核苷、核苷酸和类似物 - 嘌呤核苷
• 英文名称: N2,O6,O3',O5'-tetrakis-trimethylsilanyl-2'-deoxy-guanosine
• 英文别名: Tetrakis-trimethylsilyl-2'-desoxy-guanosin；N²,O⁶,O^3'_,O5'-tetrakis-trimethylsilanyl-2'-deoxy-guanosine
• CAS: 123389-63-9
• 化学式: C₂₂H₄₅N₅O₄Si₄
• 分子量: 555.972
• InChiKey: ILFXBGNQNBWQLE-RCCFBDPRSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.65
• 重原子数：
  35.0
• 可旋转键数：
  10.0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.77
• 拓扑面积：
  92.55
• 氢给体数：
  1.0
• 氢受体数：
  9.0

反应信息

• 作为反应物：
  描述：

  N2,O6,O3',O5'-tetrakis-trimethylsilanyl-2'-deoxy-guanosine 在 吡啶 、 4-二甲氨基吡啶 、 1-羟基苯并三唑 、 N,N-二异丙基乙胺 作用下， 以 四氢呋喃 、 乙腈 为溶剂， 反应 5.33h， 生成 N-[9-[(2R,4S,5R)-5-[[bis(4-methoxyphenyl)-phenylmethoxy]methyl]-4-[2-cyanoethoxy-[di(propan-2-yl)amino]phosphanyl]oxyoxolan-2-yl]-6-oxo-1H-purin-2-yl]-2-phenylacetamide
  参考文献：
  名称：

  The Phenylacetyl Group—The First Amino Protecting Group That Can Be Removed Enzymatically from Oligonucleotides in Solution and on a Solid Support

  摘要：

  Penicillin G acylase from E. coli was used to cleave the phenylacetyl group—the first enzyme‐labile protecting group for the amino function of nucleobases. Now protected oligonucleotides can be unmasked both in solution and on solid supports with this versatile enyzme under mild conditions (pH 7, room temperature). These results may lead to the development of new enzymatic reactions in oligonucleotide and solid‐phase chemistry as well as in combinatorial chemistry.

  DOI：

  10.1002/anie.199706471
• 作为产物：
  描述：

  三甲基氯硅烷 、 2'-脱氧鸟苷 在 吡啶 作用下， 反应 0.5h， 生成 N2,O6,O3',O5'-tetrakis-trimethylsilanyl-2'-deoxy-guanosine
  参考文献：
  名称：

  The Phenylacetyl Group—The First Amino Protecting Group That Can Be Removed Enzymatically from Oligonucleotides in Solution and on a Solid Support

  摘要：

  Penicillin G acylase from E. coli was used to cleave the phenylacetyl group—the first enzyme‐labile protecting group for the amino function of nucleobases. Now protected oligonucleotides can be unmasked both in solution and on solid supports with this versatile enyzme under mild conditions (pH 7, room temperature). These results may lead to the development of new enzymatic reactions in oligonucleotide and solid‐phase chemistry as well as in combinatorial chemistry.

  DOI：

  10.1002/anie.199706471