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Cyclic Diaryl λ(3)-Chloranes: Reagents and Their C–C and C–O Couplings with Phenols via Aryne Intermediates

[Image: see text] Hypervalent chloranes are a class of rare and poorly explored reagents. Their unique electronic properties confer reactivity that is complementary to that of the common iodanes and emerging bromanes. Highly chemo- and regioselective, metal-free, and mild C–C and C–O couplings are r...

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Detalles Bibliográficos
Autores principales: Lanzi, Matteo, Rogge, Torben, Truong, Tan Sang, Houk, K. N., Wencel-Delord, Joanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9837845/
https://www.ncbi.nlm.nih.gov/pubmed/36535642
http://dx.doi.org/10.1021/jacs.2c10090
Descripción
Sumario:[Image: see text] Hypervalent chloranes are a class of rare and poorly explored reagents. Their unique electronic properties confer reactivity that is complementary to that of the common iodanes and emerging bromanes. Highly chemo- and regioselective, metal-free, and mild C–C and C–O couplings are reported here. Experimental and computational mechanistic studies elucidate the unprecedented reactivities and selectivities of these systems and the intermediacy of aryne intermediates. The synthetic potential of these transformations is further demonstrated via the post-functionalization of C–C and C–O coupling products obtained from reactions of chloranes with phenols under different conditions.