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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...

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Detalles Bibliográficos
Autores principales: Tran, Duc N., Battilocchio, Claudio, Lou, Shing-Bong, Hawkins, Joel M., Ley, Steven V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2015
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
Descripción
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.