Cargando…
Halogenation Reactions of Alkyl Alcohols Employing Methyl Grignard Reagents
[Image: see text] Grignard reagents are commonly used as carbanion equivalents. Herein, we report an example of Grignard reagents acting as halide nucleophiles to form alkyl iodides and bromides. We establish that Grignard reagents can convert alkyl mesylates into alkyl halides, as well as be employ...
Autores principales: | Hirbawi, Nadia, Lin, Patricia C., Jarvo, Elizabeth R. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9486953/ https://www.ncbi.nlm.nih.gov/pubmed/36049783 http://dx.doi.org/10.1021/acs.joc.2c01590 |
Ejemplares similares
-
Stereospecific Nickel-Catalyzed Cross-Coupling Reactions
of Benzylic Ethers with Isotopically-Labeled Grignard Reagents
por: Dawson, David D., et al.
Publicado: (2015) -
Fe-catalyzed three-component dicarbofunctionalization of unactivated alkenes with alkyl halides and Grignard reagents
por: Liu, Lei, et al.
Publicado: (2020) -
Nickel-Catalyzed
Stereoselective Coupling Reactions
of Benzylic and Alkyl Alcohol Derivatives
por: Herbert, Claire A., et al.
Publicado: (2023) -
Iron-Catalyzed Coupling of Aryl Grignard Reagents with Alkyl Halides: A Competitive Hammett Study**
por: Hedström, Anna, et al.
Publicado: (2011) -
Iron‐Catalyzed Cross‐Coupling of Alkynyl and Styrenyl Chlorides with Alkyl Grignard Reagents in Batch and Flow
por: Deng, Yuchao, et al.
Publicado: (2019)