Synthesis of New Tetrakis N-Substituted Tetra-Azamacrocycles
C. Trabaud, Jean Dessolin, Michel Camplo, L Kraus
Abstract
C. Trabaud, Jean Dessolin, Michel Camplo, L Kraus
Abstract
The synthesis of new tetra-kis N- substituted tetra-azamacrocyles was achieved. In the case of tetra amido analogues the best yields were obtained through the use of Schotten - Bauman reaction type in a biphasic system. In the case of tetra-N- ω alkyl carboxylic esters, optimal experimental conditions leading to the desired tetra N-substituted derivatives are described.
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The synthesis of new tetra-kis N- substituted tetra-azamacrocyles was achieved. In the case of tetra amido analogues the best yields were obtained through the use of Schotten - Bauman reaction type in a biphasic system. In the case of tetra-N- ω alkyl carboxylic esters, optimal experimental conditions leading to the desired tetra N-substituted derivatives are described.
Key concepts: Tetra, Chemistry, Alkyl, Reaction conditions, Medicinal chemistry, Organic chemistry, Combinatorial chemistry, Catalysis