Abstract
δ5-3-dimethylamino-3-oxo-1,2,3-diazaphospholines are prepared by cyclisation of bis(dimethylami-no)phosphinallene oxides containing two electrophilic sites in position 1.3 (phosphorus atom and medium carbon allenic) with hydrazine derivatives. Mechanistic explanations of these results have been described by NMR. The IR and the 31P, 13C, 1H chemical shifts of diazaphosphollines oxides are commented.