Shiga Naoki, Takayanagi Shihori, Muramoto Risa, Murakami Tasuku, Qin Rui, Suzuki Yuta, Shinohara Ken-Ichi, Kaneda Atsushi, Nemoto Tetsuhiro
Graduate School of Pharmaceutical Sciences, Chiba University, 1-8-1, Inohana, Chuo-ku, Chiba 260-8675, Japan.
Graduate School of Medicine, Chiba University, 1-8-1, Inohana, Chuo-ku, Chiba 260-8670, Japan.
Bioorg Med Chem Lett. 2017 May 15;27(10):2197-2200. doi: 10.1016/j.bmcl.2017.03.052. Epub 2017 Mar 29.
Pyrrole-imidazole (Py-Im) polyamides are useful tools for chemical biology and medicinal chemistry studies due to their unique binding properties to the minor groove of DNA. We developed a novel method of synthesizing Py-Im polyamide oligomers based on a Cu-catalyzed cross-coupling strategy. All four patterns of dimer fragments could be synthesized using a Cu-catalyzed Ullmann-type cross-coupling with easily prepared monomer units. Moreover, we demonstrated that pyrrole dimer, trimer, and tetramer building blocks for Py-Im polyamide synthesis were accessible by combining site selective iodination of the pyrrole/pyrrole coupling adduct.
由于吡咯-咪唑(Py-Im)聚酰胺对DNA小沟具有独特的结合特性,它们是化学生物学和药物化学研究的有用工具。我们基于铜催化的交叉偶联策略开发了一种合成Py-Im聚酰胺低聚物的新方法。使用铜催化的乌尔曼型交叉偶联与易于制备的单体单元,可以合成所有四种模式的二聚体片段。此外,我们证明,通过结合吡咯/吡咯偶联加合物的位点选择性碘化,可以获得用于Py-Im聚酰胺合成的吡咯二聚体、三聚体和四聚体结构单元。