Department of Pharmacognosy-Pharmacology, School of Pharmacy, Aristotle University of Thessaloniki, 54124 Thessaloniki, Greece.
Int J Mol Sci. 2022 Mar 21;23(6):3395. doi: 10.3390/ijms23063395.
Compounds bearing the phosphorus-carbon (P-C) bond have important pharmacological, biochemical, and toxicological properties. Historically, the most notable reaction for the formation of the P-C bond is the Michaelis-Arbuzov reaction, first described in 1898. The classical Michaelis-Arbuzov reaction entails a reaction between an alkyl halide and a trialkyl phosphite to yield a dialkylalkylphosphonate. Nonetheless, deviations from the classical mechanisms and new modifications have appeared that allowed the expansion of the library of reactants and consequently the chemical space of the yielded products. These involve the use of Lewis acid catalysts, green methods, ultrasound, microwave, photochemically-assisted reactions, aryne-based reactions, etc. Here, a detailed presentation of the Michaelis-Arbuzov reaction and its developments and applications in the synthesis of biomedically important agents is provided. Certain examples of such applications include the development of alkylphosphonofluoridates as serine hydrolase inhibitors and activity-based probes, and the P-C containing antiviral and anticancer agents.
含有磷-碳(P-C)键的化合物具有重要的药理学、生物化学和毒理学性质。历史上,形成 P-C 键的最显著反应是 1898 年首次描述的 Michaelis-Arbuzov 反应。经典的 Michaelis-Arbuzov 反应涉及卤代烷和三烷基膦之间的反应,生成二烷基烷基膦酸酯。然而,偏离经典机制和新的修饰已经出现,允许反应物库的扩展,从而扩展产物的化学空间。这些涉及路易斯酸催化剂、绿色方法、超声、微波、光化学辅助反应、芳炔反应等的使用。在这里,详细介绍了 Michaelis-Arbuzov 反应及其在合成生物医学重要试剂中的发展和应用。此类应用的某些示例包括将烷基膦酸氟化物开发为丝氨酸水解酶抑制剂和基于活性的探针,以及含有 P-C 的抗病毒和抗癌剂。