Cargando…
Electrochemistry and Reactivity of Chelation‐stabilized Hypervalent Bromine(III) Compounds
Hypervalent bromine(III) reagents possess a higher electrophilicity and a stronger oxidizing power compared to their iodine(III) counterparts. Despite the superior reactivity, bromine(III) reagents have a reputation of hard‐to‐control and difficult‐to‐synthesize compounds. This is partly due to thei...
Autores principales: | Mohebbati, Nayereh, Sokolovs, Igors, Woite, Philipp, Lõkov, Märt, Parman, Elisabeth, Ugandi, Mihkel, Leito, Ivo, Roemelt, Michael, Suna, Edgars, Francke, Robert |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9401590/ https://www.ncbi.nlm.nih.gov/pubmed/35510557 http://dx.doi.org/10.1002/chem.202200974 |
Ejemplares similares
-
Electrochemical Generation of Hypervalent Bromine(III) Compounds
por: Sokolovs, Igors, et al.
Publicado: (2021) -
Electrochemical
Synthesis of Dimeric λ(3)-Bromane: Platform
for Hypervalent Bromine(III) Compounds
por: Sokolovs, Igors, et al.
Publicado: (2023) -
Hypervalent Iodine-Mediated Chemoselective Bromination of Terminal Alkynes
por: Li, Youzhi, et al.
Publicado: (2022) -
Multifunctional Organocatalysts ‐ Singly‐Linked and Macrocyclic Bisphosphoric Acids for Asymmetric Phase‐Transfer and Brønsted‐Acid Catalysis
por: Thiele, Maike, et al.
Publicado: (2022) -
Halogen bonding in hypervalent iodine and bromine derivatives: halonium salts
por: Cavallo, Gabriella, et al.
Publicado: (2017)