1998Synthetic CommunicationsRequires access

Synthesis of New Tetrakis N-Substituted Tetra-Azamacrocycles

C. Trabaud, Jean Dessolin, Michel Camplo, L Kraus

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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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What this paper is about

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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Available 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.

Key concepts: Tetra, Chemistry, Alkyl, Reaction conditions, Medicinal chemistry, Organic chemistry, Combinatorial chemistry, Catalysis

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