作者:Hsi-Lung Pan、Carol-Ann Cole、T.Lloyd Fletcher
DOI:10.1002/jps.2600690141
日期:1980.1
New 9-substituted 3-nitrofluorenes were prepared as potential intermediates in a study of modified electrophilicity and mutagenicity of the carcinogen 3-N,O-diacetylhydroxylaminofluorene. The reported derivatives, together with some already known 9-substituted 3-nitrofluorenes, were too unstable to survive the reducing conditions required to transform the nitro group to the corresponding hydroxylamine
在研究致癌物3-N,O-二乙酰基羟氨基芴的改良的亲电子性和致突变性的研究中,制备了新的9-取代的3-硝基芴作为潜在的中间体。所报道的衍生物与一些已知的9-取代的3-硝基芴一起不稳定,以至于不能承受将硝基转化为相应的羟胺所需的还原条件。