Cargando…
Nickel-Catalyzed Reductive Conjugate Addition of Primary Alkyl Bromides to Enones To Form Silyl Enol Ethers
[Image: see text] Conjugate addition of organometallic reagents to enones to form silyl enol ether products is a versatile method to difunctionalize activated olefins, but the organometallic reagents required can be limiting. The reductive cross-electrophile coupling of unhindered primary alkyl brom...
Autores principales: | Huihui, Kierra M. M., Shrestha, Ruja, Weix, Daniel J. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2017
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5260806/ https://www.ncbi.nlm.nih.gov/pubmed/28054785 http://dx.doi.org/10.1021/acs.orglett.6b03509 |
Ejemplares similares
-
Gold-catalyzed alkylation of silyl enol ethers with ortho-alkynylbenzoic acid esters
por: Aikawa, Haruo, et al.
Publicado: (2011) -
Photoredox-catalyzed silyldifluoromethylation of silyl enol ethers
por: Supranovich, Vyacheslav I, et al.
Publicado: (2020) -
FLP‐Catalyzed Transfer Hydrogenation of Silyl Enol Ethers
por: Khan, Imtiaz, et al.
Publicado: (2018) -
Nickel(ii)-catalyzed reductive silylation of alkenyl methyl ethers for the synthesis of alkyl silanes
por: Qiu, Xiaodong, et al.
Publicado: (2021) -
Silyl-mediated photoredox-catalyzed Giese reaction: addition of non-activated alkyl bromides
por: ElMarrouni, Abdellatif, et al.
Publicado: (2018)