Department of Chemistry, Sri Venkateswara University, Tirupati, India.
Arch Pharm (Weinheim). 2011 Nov;344(11):765-70. doi: 10.1002/ardp.201000280. Epub 2011 Sep 27.
Synthesis of 1-substituted-1,3,2-diazaphosphole 1-oxides (3a-l) were accomplished via a two-step process. It involves the preparation of diazaphospholo 1-oxide monochloride intermediate (2) and its subsequent reaction with phenols/amino acid esters in dry THF in the presence of triethylamine at 40-45°C. The structures of newly synthesized compounds were characterized by spectral and elemental analysis. The title compounds were evaluated for their in-vitro antioxidant properties.
1-取代-1,3,2-二氮杂膦氧 1-氧化物(3a-l)的合成都通过两步法来实现。该方法涉及二氮杂膦氧 1-氧化物一氯代物中间体(2)的制备,以及在三乙胺的存在下,在 40-45°C 的干燥四氢呋喃中,与酚类/氨基酸酯的后续反应。新合成化合物的结构通过光谱和元素分析来表征。对标题化合物的体外抗氧化性能进行了评估。