Cargando…
Part 2. Mechanistic aspects of the reduction of S-alkyl-thionocarbonates in the presence of triethylborane and air
Experiments conducted with deuterated compounds demonstrated that during the reduction of S-alkylxanthates with triethylborane, the hydrogen atom transferred has several competing origins. Hydrogen abstraction from water (or an alcohol) is the most favourable route.
Autores principales: | Allais, Florent, Boivin, Jean, Nguyen, Van Tai |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2007
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2213662/ https://www.ncbi.nlm.nih.gov/pubmed/18076755 http://dx.doi.org/10.1186/1860-5397-3-46 |
Ejemplares similares
-
Part 1. Reduction of S-alkyl-thionocarbonates and related compounds in the presence of trialkylboranes/air
por: Boivin, Jean, et al.
Publicado: (2007) -
Part 3. Triethylborane-air: a suitable initiator for intermolecular radical additions of S-2-oxoalkyl-thionocarbonates (S-xanthates) to olefins
por: Boivin, Jean, et al.
Publicado: (2007) -
Kinetic Model and Experiment for Self-Ignition of Triethylaluminum and Triethylborane Droplets in Air
por: Frolov, Sergey M., et al.
Publicado: (2022) -
Synthesis of bis(indolyl)methanes Catalyzed by Triethylborane
por: Merinos, J. Pablo García, et al.
Publicado: (2015) -
Diastereoselective C-alkylation of aldimines, derived from chiral α-carbon heteroatom-substituted aldehydes, with triethylborane. Application to the synthesis of benzylisoquinolines
por: Fuentes-Ríos, David, et al.
Publicado: (2023)