Abstract
Treatment of N-(2-bromoaryl) enaminones 4, prepared by several different methods, with palladium (II) acetate, triarylphosphine and triethylamine in boiling acetonitrile gave pyrrolo[1,2- a]indoles 8 yields of 50% – 100%. The hydroxy-substituted products 8k could be oxidised to the mitosene-like quinone 9 with Fremy's salt.
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