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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...
Autores principales: | Schulz, Göran, George, Vincent, Taser, Daghan, Kirschning, Andreas |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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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 |
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