Cargando…
Sterically constrained tricyclic phosphine: redox behaviour, reductive and oxidative cleavage of P–C bonds, generation of a dilithium phosphaindole as a promising synthon in phosphine chemistry
The redox behaviour of sterically constrained tricyclic phosphine 3a was investigated by spectroelectrochemistry. The data suggested a highly negative reduction potential with the reversible formation of a dianionic species. Accordingly, 3a reacted with two equivalents of Li/naphthalene by reductive...
Autores principales: | Brand, Alexander, Schulz, Stephen, Hepp, Alexander, Weigand, Jan J., Uhl, Werner |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8179454/ https://www.ncbi.nlm.nih.gov/pubmed/34163619 http://dx.doi.org/10.1039/d0sc06155g |
Ejemplares similares
-
Tetramethylphosphinane as a new secondary phosphine synthon
por: Nobbs, James D., et al.
Publicado: (2023) -
Effect
of the Phosphine Steric and Electronic Profile
on the Rh-Promoted Dehydrocoupling of Phosphine–Boranes
por: Hooper, Thomas N., et al.
Publicado: (2014) -
Sterically Controlled Late‐Stage Functionalization of Bulky Phosphines
por: Deng, Hao, et al.
Publicado: (2022) -
Synthesis and reactivity of cyclo-tetra(stibinophosphonium) tetracations: redox and coordination chemistry of phosphine–antimony complexes
por: Chitnis, Saurabh S., et al.
Publicado: (2015) -
Electronic and Steric Effects in Gold(I) Phosphine Thiolate
Complexes
por: Foley, Janet, et al.
Publicado: (1994)