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Flow chemistry as a discovery tool to access sp(2)–sp(3) cross-coupling reactions via diazo compounds
The work takes advantage of an important feature of flow chemistry, whereby the generation of a transient species (or reactive intermediate) can be followed by a transfer step into another chemical environment, before the intermediate is reacted with a coupling partner. This concept is successfully...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5811102/ https://www.ncbi.nlm.nih.gov/pubmed/29560199 http://dx.doi.org/10.1039/c4sc03072a |
Sumario: | The work takes advantage of an important feature of flow chemistry, whereby the generation of a transient species (or reactive intermediate) can be followed by a transfer step into another chemical environment, before the intermediate is reacted with a coupling partner. This concept is successfully applied to achieve a room temperature sp(2)–sp(3) cross coupling of boronic acids with diazo compounds, these latter species being generated from hydrazones under flow conditions using MnO(2) as the oxidant. |
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