一种无金属催化的活泼烯烃与全氟碘代丁烷自由基环化合成含氟吲哚酮的反应被发展.在廉价易得的的偶氮二异丁腈(AIBN)介导下,多种N-芳基丙烯酰胺类化合物与全氟碘代丁烷发生自由基串联环化反应,以53％～85％的产率合成了一系列的潜在生理活性的多氟取代吲哚酮.此工作为潜在药用价值的多氟取代吲哚酮合成提供了一条高效、廉价、绿色的新途径.
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