Reductive Cyclization of Unactivated Alkyl Chlorides with Tethered Alkenes under Visible‐Light Photoredox Catalysis

The chemical inertness of abundant and commercially available alkyl chlorides precludes their widespread use as reactants in chemical transformations. Presented in this work is a metallaphotoredox methodology to achieve the catalytic intramolecular reductive cyclization of unactivated alkyl chloride...

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Detalles Bibliográficos
Autores principales: Claros, Miguel, Ungeheuer, Felix, Franco, Federico, Martin‐Diaconescu, Vlad, Casitas, Alicia, Lloret‐Fillol, Julio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Communications
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6519206/
https://www.ncbi.nlm.nih.gov/pubmed/30707782
http://dx.doi.org/10.1002/anie.201812702

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6519206/
https://www.ncbi.nlm.nih.gov/pubmed/30707782
http://dx.doi.org/10.1002/anie.201812702

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