硒-迈克尔反应立体选择性合成4′-硒核苷

Q4 Chemistry
Pramod K. Sahu, Dnyandev B. Jarhad, Gyudong Kim, Lak Shin Jeong
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引用次数: 0

摘要

5′-同源-4′-硒核苷是由d -核糖经4-硒糖中间体合成的新一代核苷。合成该中间体的关键步骤是硒-迈克尔反应。采用pummerer缩合法和vorbrggen缩合法分别制备了5′-Homo-4′-硒脲和-腺苷。©2017 by John Wiley &儿子,Inc。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Stereoselective Synthesis of 4′-Selenonucleosides via the Seleno-Michael Reaction

5′-Homo-4′-selenonucleosides, a class of next-generation nucleosides, are synthesized from D-ribose via a 4-selenosugar intermediate. The key step in synthesizing this intermediate is a seleno-Michael reaction. 5′-Homo-4′-selenouridine and -adenosine are prepared using Pummerer-type and Vorbrüggen condensation, respectively. © 2017 by John Wiley & Sons, Inc.

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来源期刊
Current Protocols in Nucleic Acid Chemistry
Current Protocols in Nucleic Acid Chemistry Chemistry-Organic Chemistry
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期刊介绍: Published in association with International Society for Nucleosides, Nucleotides & Nucleic Acids (IS3NA) , Current Protocols in Nucleic Acid Chemistry is equally valuable for biotech, pharmaceutical, and academic labs. It is the resource for designing and running successful research projects in the rapidly growing and changing field of nucleic acid, nucleotide, and nucleoside research.
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