期刊
CHEMICAL COMMUNICATIONS
卷 54, 期 54, 页码 7443-7446出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c8cc03575j
关键词
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The development of visible-light-induced synthesis of functionalized pyrroloindolines via a radical cascade reaction is reported. The reaction shows a broad substrate scope and highlights the mild nature of the reaction conditions. A range of substitutions on indole aromatic rings and N-centers is well tolerated, including a free allylic alcohol. Relying on the strategy, a rapid synthesis of (+/-)-flustraminol B was achieved.
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