Abstract
The rearrangement, under basic conditions, of the N-ureidopyrroles (8) directly led to the pyrrolylalkenes (14). The reaction was explained in terms of initial mononuclear heterocyclic rearrangement leading to the pyrrolo[1,2-c] [1,2,3]-triazoles (12) followed by their decomposition to the final products under the reaction conditions. Attempts to thermally rearrange compound (8b) only gave products of decomposition of the ureido moiety
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