The first completely enantioselective syntheses of indicine N-oxide, intermedine N-oxide, and their enantiomers have been achieved stereospecifically. A synthetic analogue modeled on indicine N-oxide showed the superior activity to indicine N-oxide itself against cancer cell in vitro test.
首次实现了
吲哚啉N-氧化物、中间啶N-氧化物及其对映体的完全对映选择性合成,并进行了立体专一性制备。以
吲哚啉N-氧化物为模型设计的合成类似物,在体外抗癌细胞测试中显示出比
吲哚啉N-氧化物本身更优越的活性。