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Amide Synthesis by Transamidation of Primary Carboxamides (CROSBI ID 279375)

Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija

Laclef, Sylvain ; Kolympadi Marković, Maria ; Marković, Dean Amide Synthesis by Transamidation of Primary Carboxamides // Synthesis, 52 (2020), 21; 3231-242. doi: 10.1055/s-0040-1707133

Podaci o odgovornosti

Laclef, Sylvain ; Kolympadi Marković, Maria ; Marković, Dean

engleski

Amide Synthesis by Transamidation of Primary Carboxamides

The amide functionality is one of the most important and widely used groups in nature and in medicinal and industrial chemistry. Because of its importance and as the actual synthetic methods suffer from major drawbacks, such as the use of a stoichiometric amount of an activating agent, epimerization and low atom economy, the development of new and efficient amide bond forming reactions is needed. A number of greener and more effective strategies have been studied and developed. The transamidation of primary amides is particularly attractive in terms of atom economy and as ammonia is the single byproduct. This review summarizes the advancements in metal-catalyzed and organocatalyzed transamidation methods. Lewis and Brønsted acid transamidation catalysts are reviewed as a separate group. The activation of primary amides by promoter, as well as catalyst- and promoter-free protocols, are also described. The proposed mechanisms and key intermediates of the depicted transamidation reactions are shown.

primary amides - transamidation - amide bond - carbox­amides - amine formylation

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Podaci o izdanju

52 (21)

2020.

3231-242

objavljeno

0039-7881

10.1055/s-0040-1707133

Povezanost rada

nije evidentirano

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