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Nickel-catalyzed reductive cleavage of aryl alkyl ethers to arenes in absence of external reductant

The reductive cleavage of the C–O bonds of aryl ethers has great potential in organic synthesis. Although several catalysts that can promote the reductive cleavage of aryl ethers have been reported, all such systems require the use of an external reductant, e.g., hydrosilane or hydrogen. Here, we re...

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Detalles Bibliográficos
Autores principales: Tobisu, Mamoru, Morioka, Toshifumi, Ohtsuki, Akimichi, Chatani, Naoto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5659071/
https://www.ncbi.nlm.nih.gov/pubmed/29511506
http://dx.doi.org/10.1039/c5sc00305a

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