1,2-O-isopropylidene-3,5(R/S)-d2-α-D-ribofuranose | 219568-62-4

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 1,2-O-isopropylidene-3,5(R/S)-d2-α-D-ribofuranose
• 英文别名: 1,2-O-isopropylidene-α-D-ribofuranose-3,5(R/S)-2H2；(3aR,5R,6R,6aR)-6-deuterio-5-[deuterio(hydroxy)methyl]-2,2-dimethyl-5,6a-dihydro-3aH-furo[2,3-d][1,3]dioxol-6-ol
• CAS: 219568-62-4
• 化学式: C₈H₁₄O₅
• 分子量: 192.18
• InChiKey: JAUQZVBVVJJRKM-AVRCNHLFSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -0.78
• 重原子数：
  13.0
• 可旋转键数：
  1.0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  68.15
• 氢给体数：
  2.0
• 氢受体数：
  5.0

反应信息

• 作为反应物：
  描述：

  1,2-O-isopropylidene-3,5(R/S)-d2-α-D-ribofuranose 在 硫酸 、 溶剂黄146 作用下， 以 水 为溶剂， 反应 38.5h， 生成 methyl α-D-ribofuranoside-3,5(R/S)-2H2
  参考文献：
  名称：

  Synthesis of partially-deuterated 2′-deoxyribonucleoside blocks and their incorporation into an oligo-DNA for simplification of overcrowding and selective enhancement of resolution and sensitivity in the 1H-NMR spectra

  摘要：

  The chemical synthesis of appropriately protected partially-deuterated 2'((R) under bar/(S) under bar), 3',5'((R) under bar/(S) under bar)-H-2(3)-2'-deoxyribonucleoside blocks [similar to 43 atom % H-2 at C5'((R) under bar), similar to 57 atom % H-2 at C5'((S) under bar); similar to 15 atom % H-2 at C2'((R) under bar, similar to 85 atom % H-2 at C2'((S) under bar) and >99 atom % H-2 at C3'] is reported. The availability of these deuterium labelled blocks on large scale has enabled the chemical assemblage of the deuterio isotopomeric 12 mer [d((C) double under bar(1)(G) double under bar(2)(C) double under bar(3)(G) double under bar(4)(A) double under bar(5)(A) double under bar(6)(T) double under bar(7)(T) double under bar(8)(C) double under bar(9)(G) double under bar(10)(C) double under bar(11)(G) double under bar(12))](2) DNA duplex by standard solid-phase synthesis protocol in order to demonstrate the usefulness of the new "NMR-window III" approach (see the following paper). (C) 1998 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0040-4020(98)00905-3
• 作为产物：
  描述：

  1,2:5,6-di-O-isopropylidene-β-D-(3-2H)-mannose 在 硼氘化钠 、 溶剂黄146 作用下， 以 乙醇 、 水 为溶剂， 反应 20.0h， 生成 1,2-O-isopropylidene-3,5(R/S)-d2-α-D-ribofuranose
  参考文献：
  名称：

  Synthesis of partially-deuterated 2′-deoxyribonucleoside blocks and their incorporation into an oligo-DNA for simplification of overcrowding and selective enhancement of resolution and sensitivity in the 1H-NMR spectra

  摘要：

  The chemical synthesis of appropriately protected partially-deuterated 2'((R) under bar/(S) under bar), 3',5'((R) under bar/(S) under bar)-H-2(3)-2'-deoxyribonucleoside blocks [similar to 43 atom % H-2 at C5'((R) under bar), similar to 57 atom % H-2 at C5'((S) under bar); similar to 15 atom % H-2 at C2'((R) under bar, similar to 85 atom % H-2 at C2'((S) under bar) and >99 atom % H-2 at C3'] is reported. The availability of these deuterium labelled blocks on large scale has enabled the chemical assemblage of the deuterio isotopomeric 12 mer [d((C) double under bar(1)(G) double under bar(2)(C) double under bar(3)(G) double under bar(4)(A) double under bar(5)(A) double under bar(6)(T) double under bar(7)(T) double under bar(8)(C) double under bar(9)(G) double under bar(10)(C) double under bar(11)(G) double under bar(12))](2) DNA duplex by standard solid-phase synthesis protocol in order to demonstrate the usefulness of the new "NMR-window III" approach (see the following paper). (C) 1998 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0040-4020(98)00905-3

文献信息

• T1 and T2 relaxations of the 13C nuclei of deuterium‐labeled nucleosides
  作者：T. V. Maltseva、A. Földesi、J. Chattopadhyaya

  DOI：10.1002/(sici)1097-458x(199804)36:4<227::aid-omr266>3.3.co;2-0

  日期：1998.4