Cargando…
Catalytic intramolecular aminoarylation of unactivated alkenes with aryl sulfonamides
Arylethylamines are abundant motifs in myriad natural products and pharmaceuticals, so efficient methods to synthesize them are valuable in drug discovery. In this work, we disclose an intramolecular alkene aminoarylation cascade that exploits the electrophilicity of a nitrogen-centered radical to f...
Autores principales: | Noten, Efrey A., McAtee, Rory C., Stephenson, Corey R. J. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9200115/ https://www.ncbi.nlm.nih.gov/pubmed/35774166 http://dx.doi.org/10.1039/d2sc01228f |
Ejemplares similares
-
Arene dearomatization through a catalytic N-centered radical cascade reaction
por: McAtee, Rory C., et al.
Publicado: (2020) -
Nickel-catalyzed asymmetric reductive aryl-allylation of unactivated alkenes
por: Lin, Zhiyang, et al.
Publicado: (2021) -
Nickel(0)-catalyzed linear-selective hydroarylation of unactivated alkenes and styrenes with aryl boronic acids
por: Lv, Honggui, et al.
Publicado: (2018) -
Stereoconvergent
Arylations and Alkenylations of Unactivated
Alkyl Electrophiles: Catalytic Enantioselective Synthesis of Secondary
Sulfonamides and Sulfones
por: Choi, Junwon, et al.
Publicado: (2014) -
Copper-catalyzed diamination of unactivated alkenes with hydroxylamines
por: Shen, Kun, et al.
Publicado: (2015)