Abstract
AbstractThe roots of the indigenous West African shrub Cryptolepis sanguinolenta have proved to be a rich source of indoloquinoline alkaloids. To date, all of the alkaloids isolated have been analogs of indolo[3, 2‐b]quinoline. We now wish to report examples of two new indoloquinoline alkaloids which differ in the fusion of the indole and quinoline rings. The first, cryptosanguinolentine, is an angular indolo[3, 2‐c]quinoline. The second, cryptotackieine, is a linear indolo[2, 3‐b]quinoline system. Both of these families of alkaloids are without precedent from C. sanguinolenta. The structures of both were established through the extensive use of inverse‐detected micro nmr methods.
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