Cargando…
Eosin Y-Catalyzed Synthesis of 3-Aminoimidazo[1,2-a]Pyridines via the HAT Process under Visible Light through Formation of the C–N Bond
[Image: see text] A comfortable, environment-friendly, and metal-free approach for synthesizing the biologically important moiety aminoimidazopyridine through the multicomponent reaction of benzylamine, 2-aminopyridine, and t-butyl isocyanide under visible light using eosin Y as a photocatalyst has...
Autores principales: | Singh, Himanshu Kumar, Kamal, Arsala, Kumari, Savita, Kumar, Dhirendra, Maury, Suresh Kumar, Srivastava, Vandana, Singh, Sundaram |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2020
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7689671/ https://www.ncbi.nlm.nih.gov/pubmed/33251420 http://dx.doi.org/10.1021/acsomega.0c03941 |
Ejemplares similares
-
Identification of a 3-aminoimidazo[1,2-a]pyridine inhibitor of HIV-1 reverse transcriptase
por: Elleder, Daniel, et al.
Publicado: (2012) -
Eosin Y-catalyzed visible-light-mediated aerobic oxidative cyclization of N,N-dimethylanilines with maleimides
por: Liang, Zhongwei, et al.
Publicado: (2015) -
Light-accelerated depolymerization catalyzed by Eosin Y
por: Bellotti, Valentina, et al.
Publicado: (2022) -
Retraction: Eosin Y catalysed photoredox synthesis: a review
por: Srivastava, Vishal, et al.
Publicado: (2022) -
Recent application of visible-light induced radicals in C–S bond formation
por: Srivastava, Vishal, et al.
Publicado: (2020)