An improved synthetic approach to protopines based on the sequential Hofmann elimination, hydroboration and oxidation of N‐(arylmethyl)berbinium salts has been designed. By using berberine chloride as the starting material, this sequence of reactions has provided two new nonnatural protopines, N‐benzyl‐N‐nordihydroallocriptopine and N‐(p‐methoxybenzyl)‐N‐nordihydroallocriptopine and the natural allocriptopine. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2006)