作者:T. V. Kharlamova
DOI:10.1007/s10600-009-9443-6
日期:2009.9
Alkylation of 1,2-dihydroxyanthraquinone (alizarin) by α-bromoacetone was studied and its β-acetonyl derivative was chemically modified. The composition and structure of the products were confirmed by elemental analysis; UV, IR, PMR, and 13C NMR spectroscopy; and mass spectrometry. The synthesized derivatives were tested as inhibitors of HIV-1 RNase H.
对1,2-二羟基蒽醌(阿利扎林)与α-溴乙酮的烷基化进行了研究,并对其β-乙酰基衍生物进行了化学修饰。产物的组成和结构通过元素分析、紫外光谱、红外光谱、质子核磁共振(PMR)和碳-13核磁共振(13C NMR)谱以及质谱得到了确认。合成的衍生物被测试为HIV-1 RNase H的抑制剂。