核苷研究4: 3-甲硫基-7-氧代吡唑并(5, 4-e)-1, 2, 4-三嗪核苷合成研究 |
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引用本文: | 沙耀武,焦献云,蔡孟深.核苷研究4: 3-甲硫基-7-氧代吡唑并(5, 4-e)-1, 2, 4-三嗪核苷合成研究[J].有机化学,1997,17(3):256-259. |
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作者姓名: | 沙耀武 焦献云 蔡孟深 |
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作者单位: | 北京医科大学药学院 |
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摘 要: | 对3-甲硫基-7-氧代吡唑并(5, 4-e)-1, 2, 4-三嗪的成苷反应进行了研究。当保护基为乙酰基时, 生成的核苷β-体为主产物。当保护基为苯甲酰基时全部是β-体。端位构型用1H NMR确定。在五元环中, 顺位质子比反位质子裂分常数大。
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关 键 词: | 吡唑 P 质子磁共振谱法 三嗪 P 核苷 |
Studies on nucleosides IX synthesis of nucleosides of pyrazolo (5, 4-e)-1, 2, 4-triazine derivatives |
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Abstract: | The ribonucleosides of pyrazolo (5, 4-e)-1, 2, 4-triazine derivatives derivatives were synthesized. The α, β-isomes were distinguished with 1H NMR. β-isomer was the major product in acetyl protected ribonucleosides. In benzoyl protected ribonucleosides, no α-isomer was formed. The JH^1H^2 of cis isomer was bigger than that of trans in five membered ring. |
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Keywords: | PYRAZOLE P PROTON MAGNETIC RESONANCE SPECTROMETRY TRIAZINE P NUCLEOSIDE |
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