Taming Bromine Azide for Use in Organic Solvents—Radical Bromoazidations and Alcohol Oxidations

[Image: see text] The formation of bromine azide from the bisazidobromate(I) anion or alternatively from Zhdankin’s reagent, using a phosphonium bromide salt as a common starting point, is reported. After homolytic cleavage in the presence of alkenes or alcohols either 1,2-functionalization or alter...

Descripción completa

Detalles Bibliográficos
Autores principales: Schulz, Göran, George, Vincent, Taser, Daghan, Kirschning, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10028602/
https://www.ncbi.nlm.nih.gov/pubmed/36821827
http://dx.doi.org/10.1021/acs.joc.2c03012

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10028602/
https://www.ncbi.nlm.nih.gov/pubmed/36821827
http://dx.doi.org/10.1021/acs.joc.2c03012

Ejemplares similares