Manganese-catalyzed late-stage derivatization was used to construct azide-substituted tetrazolo[1,5-a]indole-containing peptides through a radical azidation/heterocyclization cascade. This electrochemical oxidative strategy could be conducted under mild, efficient, and environmentally friendly conditions in buffer solution.
锰催化后期衍生化用于通过自由基
叠氮化/杂环化级联构建
叠氮取代的
四唑并[1,5- a ]
吲哚肽。这种电
化学氧化策略可以在缓冲溶液中温和、高效、环保的条件下进行。