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Synthesis of a Protected keto-Lysidine Analogue via Improved Preparation of Arabino-isoCytosine Nucleosides

机译:通过改进的α-异型核苷的制备来合成受保护的酮 - 乙酸乙酯类似物

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摘要

Anhydrouridines react with aliphatic amines to give N-alkyl isocytosines, but reported procedures often demand very long reaction times and can be low yielding, with narrow scope. A modified procedure for such reactions has been developed, using microwave irradiation, significantly reducing reaction time and allowing facile access to a diverse range of novel nucleosides on the gram scale. The method has been used to prepare a precursor to a novel analogue of lysidine, a naturally occurring iminonucleoside found in (t)RNA.
机译:Anhydridines与脂族胺反应,得到N-烷基异型核糖,但报道的程序通常需要很长的反应时间,并且可以低产生,范围窄。 使用微波辐射产生这种反应的改性过程,显着降低了反应时间并允许容易地获得克革兰氏鳞片上的各种新型核苷。 该方法已被用于制备前体的洛塞尼的新类似物,其在(t)RNA中发现了一种天然存在的亚胺核苷。

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  • 来源
    《Organic letters》 |2019年第7期|共4页
  • 作者单位

    Univ Lancaster Dept Chem Lancaster LA1 4YB England;

    AstraZeneca Pharmaceut Dev Global Chem Dev S46 4 Silk Rd Business Pk Macclesfield SK10 2NA Cheshire England;

    Univ Huddersfield Sch Appl Sci Dept Chem Sci Huddersfield HD1 3DH W Yorkshire England;

    Univ Reading Sch Chem Food &

    Pharm POB 224 Reading RG6 6AP Berks England;

    Univ Huddersfield Sch Appl Sci Dept Chem Sci Huddersfield HD1 3DH W Yorkshire England;

    Univ Huddersfield Sch Appl Sci Dept Chem Sci Huddersfield HD1 3DH W Yorkshire England;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 有机化学;
  • 关键词

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