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使用邻硝基苄基进行2'-羟基保护和H-膦酸酯化学法固相合成寡核糖核苷酸。

Solid phase synthesis of oligoribonucleotides using the o-nitrobenzyl group for 2'-hydroxyl protection and H-phosphonate chemistry.

作者信息

Tanaka T, Tamatsukuri S, Ikehara M

机构信息

Faculty of Pharmaceutical Sciences, Osaka University, Japan.

出版信息

Nucleic Acids Res. 1987 Sep 25;15(18):7235-48. doi: 10.1093/nar/15.18.7235.

Abstract

Oligoribonucleotides with chain length of 7, 11, 15, 17, 24 and 34 were synthesized on long chain alkylamine controlled pore glass beads (LCA-CPG) using o-nitrobenzyl protection of 2'-hydroxyls via a H-phosphonate approach either manually or by using an automatic synthesizer. The oligoribonucleotides were obtained in yields of 0.6 0.6-20%, based on initial nucleoside bound to the LCA-CPG support.

摘要

链长为7、11、15、17、24和34的寡核糖核苷酸是通过H-膦酸酯法,在长链烷基胺控制孔径玻璃珠(LCA-CPG)上,采用邻硝基苄基对2'-羟基进行保护,手动或使用自动合成仪合成的。基于与LCA-CPG载体结合的初始核苷,寡核糖核苷酸的产率为0.6%-20%。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ed6/306245/fbd5b3b25b2c/nar00262-0044-a.jpg

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