Sato Kousuke, Hirose Wataru, Matsuda Akira
Faculty of Pharmaceutical Sciences, Hokkaido University, Sapporo, Japan.
Curr Protoc Nucleic Acid Chem. 2008 Dec;Chapter 1:Unit 1.21. doi: 10.1002/0471142700.nc0121s35.
A straightforward, efficient method for the synthesis of 5-formyl-2'-deoxyuridine (dfU) and solid-phase synthesis of oligodeoxynucleotides containing dfU using a phosphoramidite method are described. The synthesis of dfU is achieved by oxidation of the 5-methyl group in thymidine derivatives. However, incorporation of the dfU 3'-O-phosphoramidite into oligodeoxynucleotides proceeds in low yield, due to instability of the 5-formyl group under conditions used for automated DNA synthesis. Therefore, oligodeoxynucleotides containing a 5-(1,2-dihydroxyethyl)uracil derivative are first prepared and finally oxidized by periodate to give the desired oligodeoxynucleotides containing 5-formyluracil.
本文描述了一种合成5-甲酰基-2'-脱氧尿苷(dfU)的直接、高效方法,以及使用亚磷酰胺法固相合成含dfU的寡脱氧核苷酸的方法。dfU的合成是通过胸腺嘧啶衍生物中5-甲基的氧化来实现的。然而,由于5-甲酰基在自动DNA合成所用条件下不稳定,dfU 3'-O-亚磷酰胺掺入寡脱氧核苷酸的产率较低。因此,首先制备含5-(1,2-二羟乙基)尿嘧啶衍生物的寡脱氧核苷酸,最后用过碘酸盐氧化,得到所需的含5-甲酰基尿嘧啶的寡脱氧核苷酸。