嘧啶烯基无环核苷膦酸酯的制备

Q4 Chemistry
Elisa Pileggi, Michaela Serpi, Fabrizio Pertusati
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引用次数: 2

摘要

本合成方案描述了制备嘧啶烯基无环核苷膦酸酯(ANPs)的两种策略,包括线性和三取代烯基衍生物。在第一个过程中,母体烯基ANPs的双三甲基硅基酯是与所需氨基酸酯和芳基醇反应的关键中间体。在第二个过程中,带有ProTide促进基团的烯丙基磷酰胺是与烷基化核碱基交叉复分解反应的关键合成物,用作烯烃伙伴。©2018 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。
Preparation of Pyrimidine Alkenyl Acyclic Nucleoside Phosphonoamidates

This synthetic protocol describes two strategies for the preparation of pyrimidine alkenyl acyclic nucleoside phosphonoamidates (ANPs), including linear and trisubstituted alkenyl derivatives. For the first procedure, a bis-trimethylsilyl ester of the parent alkenyl ANPs is the key intermediate that reacts with the desired amino acid ester and aryl alcohol. For the second procedure, an allyl phosphonoamidate bearing the ProTide promoieties is the key synthon employed as olefin partner for a cross-metathesis reaction with an alkylated nucleobase. © 2018 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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