Cargando…
Ru(II)Porphyrinate-based molecular nanoreactor for carbene insertion reactions and quantitative formation of rotaxanes by active-metal-template syntheses
Selectivity in N–H and S–H carbene insertion reactions promoted by Ru(II)porphyrinates currently requires slow addition of the diazo precursor and large excess of the primary amine and thiol substrates in the reaction medium. Such conditions are necessary to avoid the undesirable carbene coupling an...
Autores principales: | Fontana, Liniquer A., Almeida, Marlon P., Alcântara, Arthur F. P., Rigolin, Vitor H., Ribeiro, Marcos A., Barros, Wdeson P., Megiatto, Jackson D. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7733472/ https://www.ncbi.nlm.nih.gov/pubmed/33311502 http://dx.doi.org/10.1038/s41467-020-20046-x |
Ejemplares similares
-
N‐Heterocyclic Carbenes: Molecular Porters of Surface Mounted Ru‐Porphyrins
por: Knecht, Peter, et al.
Publicado: (2022) -
Porphyrin–Polyyne [3]- and [5]Rotaxanes
por: Kohn, Daniel R., et al.
Publicado: (2017) -
Natural aluminosilicate nanotubes loaded with RuCo as nanoreactors for Fischer-Tropsch synthesis
por: Mazurova, Kristina, et al.
Publicado: (2022) -
Isocyanate-Free
Polyurea Synthesis via Ru-Catalyzed
Carbene Insertion into the N–H Bonds of Urea
por: de Zwart, Felix J., et al.
Publicado: (2022) -
Polymer tube nanoreactors via DNA-origami templated synthesis
por: Tokura, Yu, et al.
Publicado: (2018)