Pregled bibliografske jedinice broj: 1065218
Amide Synthesis by Transamidation of Primary Carboxamides
Amide Synthesis by Transamidation of Primary Carboxamides // Synthesis, 52 (2020), 21; 3231-242 doi:10.1055/s-0040-1707133 (međunarodna recenzija, članak, znanstveni)
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Naslov
Amide Synthesis by Transamidation of
Primary Carboxamides
Autori
Laclef, Sylvain ; Kolympadi Marković, Maria ; Marković, Dean
Izvornik
Synthesis (0039-7881) 52
(2020), 21;
3231-242
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
primary amides - transamidation - amide bond - carboxamides - amine formylation
Sažetak
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.
Izvorni jezik
Engleski
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus