Cargando…
Amide Bond Formation via the Rearrangement of Nitrile Imines Derived from N-2-Nitrophenyl Hydrazonyl Bromides
[Image: see text] We report how the rearrangement of highly reactive nitrile imines derived from N-2-nitrophenyl hydrazonyl bromides can be harnessed for the facile construction of amide bonds. This amidation reaction was found to be widely applicable to the synthesis of primary, secondary, and tert...
Autores principales: | Boyle, Mhairi, Livingstone, Keith, Henry, Martyn C., Elwood, Jessica M. L., Lopez-Fernandez, J. Daniel, Jamieson, Craig |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8762704/ https://www.ncbi.nlm.nih.gov/pubmed/34964648 http://dx.doi.org/10.1021/acs.orglett.1c03993 |
Ejemplares similares
-
Functionalized
Tetrazoles as Latent Active Esters
in the Synthesis of Amide Bonds
por: Elwood, Jessica M. L., et al.
Publicado: (2022) -
Metal-free C–C bond formation via coupling of nitrile imines and boronic acids
por: Livingstone, Keith, et al.
Publicado: (2019) -
Ultrafast Dynamics of Photochemical Nitrile Imine Formation
por: Flesch, Stefan, et al.
Publicado: (2022) -
Grignard Reagent-Catalyzed Hydroboration of Esters, Nitriles, and Imines
por: Han, Hyun Ji, et al.
Publicado: (2023) -
Hydroboration of nitriles and imines by highly active zinc dihydride catalysts
por: Wang, Xiaoming, et al.
Publicado: (2021)