Cargando…
Sequential olefination–dimerisation of benzylic dithioacetals by the nickel-catalysed reaction with methyl Grignard or zinc reagent
Products of main group elements from cross-coupling reactions have been shown to serve as Lewis acids, mediating further reactions of organic coupling products. Thus, the nickel-catalysed olefination of benzylic dithioacetal with MeMgI in benzene in a sealed Schlenk tube at 130 °C generates magnesiu...
Autores principales: | Yu, Lei, Lai, Guo-Qiao, Zhang, Pinglu, Li, Ze, Luh, Tien-Yau |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8959447/ https://www.ncbi.nlm.nih.gov/pubmed/35424913 http://dx.doi.org/10.1039/d2ra00841f |
Ejemplares similares
-
Stereospecific Nickel-Catalyzed Cross-Coupling Reactions
of Benzylic Ethers with Isotopically-Labeled Grignard Reagents
por: Dawson, David D., et al.
Publicado: (2015) -
Nickel-catalysed retro-hydroamidocarbonylation of aliphatic amides to olefins
por: Hu, Jiefeng, et al.
Publicado: (2017) -
Nickel-catalysed migratory hydroalkynylation and enantioselective hydroalkynylation of olefins with bromoalkynes
por: Jiang, Xiaoli, et al.
Publicado: (2021) -
Cross-Coupling Reaction of Allylic Ethers with Aryl Grignard Reagents Catalyzed by a Nickel Pincer Complex
por: Hashimoto, Toru, et al.
Publicado: (2019) -
Pd-catalyzed allylative dearomatisation using Grignard reagents
por: Boldrini, Cosimo, et al.
Publicado: (2021)