Cargando…
Chalcogen‐Transfer Rearrangement: Exploring Inter‐ versus Intramolecular P−P Bond Activation
tert‐Butyl‐substituted diphospha[2]ferrocenophane has been used as a stereochemically confined diphosphane to explore the addition of O, S, Se and Te. Although the diphosphanylchalcogane has been obtained for tellurium, all other chalcogens give diphosphane monochalcogenides. The latter transform vi...
Autores principales: | Franz, Roman, Nasemann, Sina, Bruhn, Clemens, Kelemen, Zsolt, Pietschnig, Rudolf |
---|---|
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/PMC7839705/ https://www.ncbi.nlm.nih.gov/pubmed/32678960 http://dx.doi.org/10.1002/chem.202002481 |
Ejemplares similares
-
Phosphetes via Transition Metal Free Ring Closure – Taking the Proper Turn at a Thermodynamic Crossing
por: Roesler, Fabian, et al.
Publicado: (2021) -
Stereochemical Alignment in Triphospha[3]ferrocenophanes
por: Borucki, Stefan, et al.
Publicado: (2017) -
Bis‐[3]Ferrocenophanes with Central >E−E’< Bonds (E, E’=P, SiH): Preparation, Properties, and Thermal Activation
por: Isenberg, Stefan, et al.
Publicado: (2019) -
Gradual Donor
Stabilization of a Transient Ferrocene
Bridged Bisphosphanyl Phosphenium Cation
por: Franz, Roman, et al.
Publicado: (2023) -
C(2)-Symmetric P-Stereogenic Ferrocene Ligands with Heavier Chalcogenophosphinous Acid Ester Donor Sites †
por: Franz, Roman, et al.
Publicado: (2021)