Department of Bioorganic Chemistry, Faculty of Chemistry, Wrocław University of Science and Technology, Wybrzeże Wyspiańskiego 27, 50-370 Wrocław, Poland.
Department of Inorganic and Structural Chemistry, Faculty of Chemistry, University of Opole, ul. Oleska 48, 45-052 Opole, Poland.
Molecules. 2023 Mar 31;28(7):3135. doi: 10.3390/molecules28073135.
A one-pot lithiation-phosphonylation procedure was elaborated as a method to prepare heteroaromatic phosphonic acids. It relied on the direct lithiation of heteroaromatics followed by phosphonylation with diethyl chlorophosphite and then oxidation with hydrogen peroxide. This protocol provided the desired phosphonates with satisfactory yields. This procedure also had some limitations in its dependence on the accessibility and stability of the lithiated heterocyclic compounds. The same procedure could be applied to phosphonylation of aromatic compounds, which do not undergo direct lithiation and thus require the use of their bromides as substrates. The obtained compounds showed weak antiproliferative activity when tested on three cancer cell lines.
一种一锅法的锂化-膦酰化方法被开发出来,用于制备杂芳基膦酸。它依赖于杂芳环的直接锂化,然后与二乙基氯膦酸酯进行膦酰化,再用过氧化氢进行氧化。该方案以令人满意的产率得到了所需的膦酸酯。该方法还存在一些局限性,即依赖于可及性和稳定性的锂化杂环化合物。同样的方法可以应用于芳基化合物的膦酰化,这些化合物不能直接锂化,因此需要使用它们的溴化物作为底物。在三种癌细胞系上进行测试时,所得到的化合物显示出较弱的抗增殖活性。