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meta-Selective olefination of fluoroarenes with alkynes using CO(2) as a traceless directing group

Over the last few decades C–H olefination has received significant interest, due to the importance and usefulness of aryl olefins both as synthetic targets and intermediates. While a wide range of ortho-olefination protocols have been developed, only a small number of meta-olefinations are currently...

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Detalles Bibliográficos
Autores principales: Spencer, Andrew R. A., Korde, Rishi, Font, Marc, Larrosa, Igor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8152615/
https://www.ncbi.nlm.nih.gov/pubmed/34122883
http://dx.doi.org/10.1039/d0sc01138j
Descripción
Sumario:Over the last few decades C–H olefination has received significant interest, due to the importance and usefulness of aryl olefins both as synthetic targets and intermediates. While a wide range of ortho-olefination protocols have been developed, only a small number of meta-olefinations are currently available. Importantly, the most common approach to meta-olefination, using a large meta-directing template, is not suitable for substrates such as fluorobenzenes, which cannot be derivatised. We report that the meta-selective olefination of fluoroarenes can be achieved via the use of CO(2) as a traceless directing group, which can be easily installed and removed in a one-pot process. Furthermore, this approach avoids the use of stoichiometric Ag(i)-salts, commonly used in C–H olefinations, and affords complete meta- over ortho/para-regioselectivity.