Cargando…
Visible Light‐Enabled sp(3)‐C−H Functionalization with Chloro‐ and Bromoalkynes: Chemoselective Route to Vinylchlorides or Alkynes
An unprecedented direct atom‐economic chemo‐ and regioselective hydroalkylation of chloroalkynes and an sp(3)‐C−H alkynylation of bromoalkynes was achieved. The reaction partners are unfunctionalized ethers, alcohols, amides, and even non‐activated hydrocarbons. We found that a household fluorescent...
Autores principales: | Adak, Tapas, Hoffmann, Marvin, Witzel, Sina, Rudolph, Matthias, Dreuw, Andreas, Hashmi, A. Stephen K. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7756539/ https://www.ncbi.nlm.nih.gov/pubmed/32472581 http://dx.doi.org/10.1002/chem.202001259 |
Ejemplares similares
-
Hypervalent Iodine-Mediated Chemoselective Bromination of Terminal Alkynes
por: Li, Youzhi, et al.
Publicado: (2022) -
Nickel-catalysed migratory hydroalkynylation and enantioselective hydroalkynylation of olefins with bromoalkynes
por: Jiang, Xiaoli, et al.
Publicado: (2021) -
Chemoselectivity of Tertiary Azides in Strain‐Promoted Alkyne‐Azide Cycloadditions
por: Svatunek, Dennis, et al.
Publicado: (2018) -
Coupling of α,α-difluoro-substituted organozinc reagents with 1-bromoalkynes
por: Zemtsov, Artem A, et al.
Publicado: (2015) -
Ruthenium-Catalyzed Peri- and Ortho-Alkynylation with Bromoalkynes via Insertion and Elimination
por: Tan, Eric, et al.
Publicado: (2017)