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通过光驱动自由基-极性交叉反应合成叔烷基膦酸酯寡核苷酸。

Synthesis of tertiary alkylphosphonate oligonucleotides through light-driven radical-polar crossover reactions.

作者信息

Ota Kenji, Nagao Kazunori, Hata Dai, Sugiyama Haruki, Segawa Yasutomo, Tokunoh Ryosuke, Seki Tomohiro, Miyamoto Naoya, Sasaki Yusuke, Ohmiya Hirohisa

机构信息

Institute for Chemical Research, Kyoto University, Uji, Kyoto, Japan.

Research, Takeda Pharmaceutical Company Limited, Fujisawa, Kanagawa, Japan.

出版信息

Nat Commun. 2023 Oct 31;14(1):6856. doi: 10.1038/s41467-023-42639-y.

Abstract

Chemical modification of nucleotides can improve the metabolic stability and target specificity of oligonucleotide therapeutics, and alkylphosphonates have been employed as charge-neutral replacements for naturally-occurring phosphodiester backbones in these compounds. However, at present, the alkyl moieties that can be attached to phosphorus atoms in these compounds are limited to methyl groups or primary/secondary alkyls, and such alkylphosphonate moieties can degrade during oligonucleotide synthesis. The present work demonstrates the tertiary alkylation of the phosphorus atoms of phosphites bearing two 2'-deoxynuclosides. This process utilizes a carbocation generated via a light-driven radical-polar crossover mechanism. This protocol provides tertiary alkylphosphonate structures that are difficult to synthesize using existing methods. The conversion of these species to oligonucleotides having charge-neutral alkylphosphonate linkages through a phosphoramidite-based approach was also confirmed in this study.

摘要

核苷酸的化学修饰可以提高寡核苷酸疗法的代谢稳定性和靶向特异性,并且烷基膦酸酯已被用作这些化合物中天然存在的磷酸二酯主链的电荷中性替代物。然而,目前,这些化合物中可连接到磷原子上的烷基部分仅限于甲基或伯/仲烷基,并且这种烷基膦酸酯部分在寡核苷酸合成过程中可能会降解。目前的工作展示了带有两个2'-脱氧核苷的亚磷酸酯磷原子的叔烷基化。该过程利用通过光驱动自由基-极性交叉机制产生的碳正离子。该方案提供了使用现有方法难以合成的叔烷基膦酸酯结构。在本研究中还证实了通过基于亚磷酰胺的方法将这些物质转化为具有电荷中性烷基膦酸酯连接的寡核苷酸。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb0e/10618202/d32f0be4783b/41467_2023_42639_Fig1_HTML.jpg

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