Department of Chemistry, Hanyang University, Sungdong-Gu, Seoul 133-791, Korea.
J Am Chem Soc. 2010 Feb 17;132(6):1792-3. doi: 10.1021/ja9106226.
We have developed an efficient method for the synthesis of 2,3-disubstituted indoles from alkyne iminoethers 1 that employs a domino process involving Ag-catalyzed condensation followed by a tandem Ag-induced cycloisomerization and 1,3-alkenyl shift to Ag-activated carbon. This methodology can be useful in regioselectively constructing 3-alkylated indoles, which are part of the structures of biologically active compounds and important alkaloids.
我们开发了一种从炔基亚胺醚 1 高效合成 2,3-二取代吲哚的方法,该方法涉及串联的 Ag 催化缩合、Ag 诱导的环化异构化和 1,3-烯基迁移到 Ag 活化的碳上的多步反应。这种方法在区域选择性构建 3-烷基化吲哚方面很有用,3-烷基化吲哚是生物活性化合物和重要生物碱的结构部分。