1-[(4-methoxycarbonylphenyl)ethynyl]-1,2-dideoxy-3,5-di-O-(4-toluoyl)-α-D-ribofuranose | 1207741-09-0

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 1-[(4-methoxycarbonylphenyl)ethynyl]-1,2-dideoxy-3,5-di-O-(4-toluoyl)-α-D-ribofuranose
• 英文别名: [(2R,3S,5S)-5-[2-(4-methoxycarbonylphenyl)ethynyl]-3-(4-methylbenzoyl)oxyoxolan-2-yl]methyl 4-methylbenzoate
• CAS: 1207741-09-0
• 化学式: C₃₁H₂₈O₇
• 分子量: 512.559
• InChiKey: OQRQOJNLULKNAB-OZNIXHKMSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.9
• 重原子数：
  38
• 可旋转键数：
  10
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.26
• 拓扑面积：
  88.1
• 氢给体数：
  0
• 氢受体数：
  7

反应信息

• 作为产物：
  描述：

  1α-ethynyl-1,2-dideoxy-3,5-di-O-(4-toluoyl)-D-ribofuranose 、 4-碘苯甲酸甲酯 在 双(乙腈)氯化钯(II) 、 caesium carbonate 、 2-二环己基磷-2,4,6-三异丙基联苯 作用下， 以 乙腈 为溶剂， 反应 2.0h， 以53%的产率得到1-[(4-methoxycarbonylphenyl)ethynyl]-1,2-dideoxy-3,5-di-O-(4-toluoyl)-α-D-ribofuranose
  参考文献：
  名称：

  Sonogashira reactions of α- and β-1-ethynyl-2-deoxyribosides: synthesis of acetylene-extended C-nucleosides

  摘要：

  An improved practical protocol for the synthesis of both anomers of 1-ethynyl-2-deoxiribosides 1 was developed. The Sonogashira coupling of ethynyldeoxyribosides 1 with various aryl- and heteroaryl halides was carried out under various conditions. It was found that the use of copper-free coupling protocols could reduce the oxidative dimerisation in favour of arylalkynyldeoxyriboside formation. (C) 2009 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2009.11.030

文献信息

• Sonogashira reactions of α- and β-1-ethynyl-2-deoxyribosides: synthesis of acetylene-extended C-nucleosides
  作者：Tomáš Bobula、Michal Hocek、Martin Kotora

  DOI：10.1016/j.tet.2009.11.030

  日期：2010.1

  An improved practical protocol for the synthesis of both anomers of 1-ethynyl-2-deoxiribosides 1 was developed. The Sonogashira coupling of ethynyldeoxyribosides 1 with various aryl- and heteroaryl halides was carried out under various conditions. It was found that the use of copper-free coupling protocols could reduce the oxidative dimerisation in favour of arylalkynyldeoxyriboside formation. (C) 2009 Elsevier Ltd. All rights reserved.