1-<5-O-tert-butyldiphenylsilyl)-2,3-dideoxy-2-phenylthio-α-D-erythro-pentofuranosyl>uracil | 132336-17-5

• 分子结构分类: 有机化合物 - 核苷、核苷酸和类似物 - 嘧啶核苷
• 英文名称: 1-<5-O-tert-butyldiphenylsilyl)-2,3-dideoxy-2-phenylthio-α-D-erythro-pentofuranosyl>uracil
• 英文别名: 1-[(2S,3R,5S)-5-[[tert-butyl(diphenyl)silyl]oxymethyl]-3-phenylsulfanyloxolan-2-yl]pyrimidine-2,4-dione
• CAS: 132336-17-5
• 化学式: C₃₁H₃₄N₂O₄SSi
• 分子量: 558.773
• InChiKey: WIMXSPPQNSDBSP-LCRMXPIESA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.56
• 重原子数：
  39.0
• 可旋转键数：
  8.0
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.29
• 拓扑面积：
  73.32
• 氢给体数：
  1.0
• 氢受体数：
  6.0

反应信息

• 作为产物：
  描述：

  1-O-acetyl-5-O-(tert-butyldiphenylsilyl)-2,3-dideoxy-2-phenylthio-D-erythro-pentofuranose 、 2,4-二(三甲硅氧基)嘧啶 生成 1-<5-O-tert-butyldiphenylsilyl)-2,3-dideoxy-2-phenylthio-α-D-erythro-pentofuranosyl>uracil
  参考文献：
  名称：

  KAWAKAMI, HIROSHI;EBATA, TAKASHI;KOSEKI, KOSHI;MATSUSHITA, HAJIME;NAOI, Y+, CHEM. LETT.,(1990) N, C. 1459-1462

  摘要：

  DOI：

文献信息

• Stereoselectivity in the Coupling Reaction between 2-Phenylthio-2,3-dideoxyribose and Silylated Pyrimidine Bases
  作者：Hiroshi Kawakami、Takashi Ebata、Koshi Koseki、Hajime Matsushita、Yoshitake Naoi、Kazuo Itoh

  DOI：10.1246/cl.1990.1459

  日期：1990.8

  Coupling reaction between 2-α-phenylthio-2,3-dideoxyribose and silylated pyrimidine bases in the presence of SnCl4 proceeded stereoselectively to give the β-anomers. These nucleosides were converted to 2′,3′-dideoxy-2′,3′-didehydronucleosides by oxidation followed by thermal elimination.

  在SnCl4存在下，2-α-苯硫基-2,3-双脱氧核糖与硅化嘧啶碱基的耦合反应以立体选择性方式进行，得到β-异构体。这些核苷随后通过氧化后进行热消除，转化为2′,3′-双脱氧-2′,3′-双脱氢核苷。
• Furanoid Glycal as a Starting Material for Nucleoside Derivatives
  作者：Hiroshi Kawakami、Takashi Ebata、Koshi Koseki、Koji Okano、Katsuya Matsumoto、Hajime Matsushita

  DOI：10.3987/com-93-6503

  日期：——

  Furanoid glycal was utilized as a starting material for the nucleoside derivatives with the aid of benzenesulfenyl chloride. Condensation reaction with silylated nucleic bases was high in the presence of SnCl4. Electrophilic addition of benzenesulfenyl chloride to the glycal with substituent also proceeded in high stereoselectivity. Phenylthio-substituted nucleoside was used to convert 2',3'-dideoxynucleoside and 2',3'-didehydro-2',3'-dideoxynucleoside.
• Synthesis of 2',3'-Didehydro-2',3'-dideoxynucleosides Utilizing Coupling Reactions between Nucleic Bases and Phenylthio-substituted 2,3-Dideoxyribose
  作者：Hiroshi Kawakami、Takashi Ebata、Koshi Koseki、Katsuya Matsumoto、Hajime Matsushita、Yoshitake Naoi、Kazuo Ito

  DOI：10.3987/com-91-5884

  日期：——

  Stereoselectivities in coupling reactions between silylated pyrimidine bases and 3- or 2-alpha-phenylthio-2,3-dideoxyribose were examined. In the former case, no stereoselectivies were observed when the coupling reactions were performed either with 1-chlorosugar in an S(N)2 mode or in the presence of Lewis acids as catalyst in an S(N)1 mode. Coupling reaction with 2-alpha-phenylthio-2,3-dideoxyribose in the presence of Lewis acids, especially SnCl4, proceeded with good stereoselectivity to give anomeric mixtures of alpha:beta = 1:9. All these nucleosides were converted to 2',3'-didehydro-2',3'-dideoxynucleosides by oxidation to sulfoxides followed by thermal elimination of sulfenic acid.