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en exploitant des travaux antérieurs concernant la synthèse d'?-hydrazinoesters et de N-aminodipeptides. L'étude de la réactivité de cette pseudoproline a permis de définir les meilleures conditions de formations de pseudotripeptides de formule P 1 -AA 1 -?-azaPro-AA 3 -P 3 . Elle a également orienté les travaux, dans un second temps, vers la synthèse de pseudopeptides incorporant un motif acide pyrazolique. Enfin, la structure des composés préparés a été analysée par RMN, IR et par modélisation moléculaire. L'examen des P 1 -AA 1 -?-azaPro(Boc)-AA 3 -P 3 a révélé la formation par liaison hydrogène d'un pseudocycle en C 7 ,