Synthesis of new racemic a-heterocyclic a,a-diaminoesters and a-aminoester carboxylic

Mabrouk El Houssine (1) , Adelrhani Elachqar (1) , Abdelilah El Hallaoui (1) , Anouar Alami (1) , Soumia El Hajji (1) , Jean Martinez (2) , Valérie Rolland (2)

1 Laboratoire de Chimie Organique
2 IBMM - Institut des Biomolécules Max Mousseron [Pôle Chimie Balard]

New racemic a-aminoester and a,a-diaminoesters derivatives were synthesized by nucleophilic substitution of methyl a-azido glycinate N-benzoylated with 3-amino-1,2,4-triazole, 2-tetrahydrofuran-2-ylmethan-amine and 2-methyl quinolin-4-amine.

Mots clés: Amino acid; Amine; Heterocyclic molecules; Nucleophilic substitution; Methyl a-azido glycinate

Domaines: Chimie organique

Mabrouk El Houssine, Adelrhani Elachqar, Abdelilah El Hallaoui, Anouar Alami, Soumia El Hajji, et al.. Synthesis of new racemic a-heterocyclic a,a-diaminoesters and a-aminoester carboxylic. Arabian Journal of Chemistry, 2013, 6, pp.93-96. ⟨10.1016/j.arabjc.2010.09.023⟩. ⟨hal-00782572⟩