Department of Chemistry, Sri Venkateswara University, Tirupati, Andhra Pradesh 517 502, India.
Eur J Med Chem. 2010 May;45(5):1828-32. doi: 10.1016/j.ejmech.2010.01.019. Epub 2010 Jan 20.
Synthesis of 3,3'-(1,4-phenylene)-bis[2-alkoxycarbonyl-alkyl)-2-thio-benzoxaphos-phinines] (3a-j) were accomplished via two step process. It involves the prior preparation of monochloride intermediate (2) and its subsequent reaction with the amino acid esters in dry tetrahydrofuran-toluene in the presence of triethylamine at reflux temperature. These compounds were characterized by IR, 1H, 13C, 31P NMR and were found to exhibit potent in vitro antioxidant activity.
3,3'-(1,4-亚苯基)-双[2-烷氧基羰基-烷基)-2-硫代苯并恶磷杂环戊二烯](3a-j)的合成都通过两步法完成。它包括先制备一氯中间产物(2),然后在三乙胺存在下,在回流温度下,在干燥的四氢呋喃-甲苯中与氨基酸酯反应。这些化合物通过 IR、1H、13C、31P NMR 进行了表征,并被发现具有很强的体外抗氧化活性。