Abstract

AbstractA large number of diversely functionalized analogs of the bioactive natural products neocryptolepine and isocryptolepine have been prepared from a series of 3‐bromoquinoline derivatives. The neocryptolepines were obtained by a Pd0‐catalyzed C−C bond coupling followed by C−N bond formation in yields up to 80 %, whereas the indoloquinolines were prepared by a Suzuki‐Miyaura cross‐coupling followed by azidation‐photochemical cyclization in yields ranging from traces to 95 % yield.

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