Ordoñez Mario, Argüello Velasco Rubén Oswaldo
Centro de Investigaciones Químicas-IICBA, Universidad Autónoma del Estado de Morelos, Av. Universidad 1001, Cuernavaca 62209, Morelos, Mexico.
Facultad de Ciencias Químicas e Ingeniería, Universidad Autónoma del Estado de Morelos, Av. Universidad 1001, Cuernavaca 62209, Morelos, Mexico.
Pharmaceuticals (Basel). 2025 Jul 18;18(7):1063. doi: 10.3390/ph18071063.
In recent years, amino--bisphosphonic acids and their esters have been considered a family of compounds of great chemical and pharmacological interest due to their important biological properties and their value as key synthons in the synthesis of more complex molecules with biological interest. This explains why several research groups are interested in developing new methods for the preparation of these compounds. Therefore, we would like to report here a summary of the synthetic strategies published in the last fifteen years for the synthesis of acyclic and heterocyclic α-, β- and γ-amino-gem-bisphosphonates, as well as their application in the preparation of selected compounds of chemical and pharmacological interest. This information can be of general knowledge to researchers working in this area, as it provides the starting point for new methods and applications of these compounds.
近年来,氨基双膦酸及其酯类化合物因其重要的生物学特性以及作为合成具有生物学意义的更复杂分子的关键合成子的价值,而被视为一类具有重大化学和药理学研究价值的化合物。这就解释了为什么几个研究小组都对开发制备这些化合物的新方法感兴趣。因此,我们在此想报告过去十五年间发表的关于合成无环和杂环α-、β-和γ-氨基偕二膦酸酯的合成策略总结,以及它们在制备具有化学和药理学研究价值的特定化合物中的应用。这些信息对于该领域的研究人员来说可能是常识性的,因为它为这些化合物的新方法和应用提供了起点。