Cargando…
One-Pot, Telescoped Alkenylation of Amides via Stable Tetrahedral Intermediates as Lithium Enolate Precursors
[Image: see text] A mild and efficient telescoped procedure for the stereoselective alkenylation of simple, non-activated amides using LiCH(2)SiMe(3) and carbonyl compounds as surrogates of alkenyllithium reagents is reported. Our methodology relies on the formation of stable tetrahedral intermediat...
Autores principales: | Ghinato, Simone, Meazzo, Carolina, De Nardi, Federica, Maranzana, Andrea, Blangetti, Marco, Prandi, Cristina |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10243110/ https://www.ncbi.nlm.nih.gov/pubmed/37218660 http://dx.doi.org/10.1021/acs.orglett.3c01269 |
Ejemplares similares
-
Chemoselective
Intermolecular Cross-Enolate-Type Coupling
of Amides
por: Kaiser, Daniel, et al.
Publicado: (2017) -
C7‐Indole Amidations and Alkenylations by Ruthenium(II) Catalysis
por: Choi, Isaac, et al.
Publicado: (2020) -
One-Pot Synthesis of Amide-Functional Main-Chain Polybenzoxazine Precursors
por: Durukan, Canan, et al.
Publicado: (2019) -
Design of a New Chiral Deep Eutectic Solvent Based on 3-Amino-1,2-propanediol and Its Application in Organolithium Chemistry
por: Antenucci, Achille, et al.
Publicado: (2022) -
Tetrahedral M(4)(μ(4)-O)
Motifs Beyond Zn: Efficient One-Pot Synthesis of Oxido–Amidate
Clusters via a Transmetalation/Hydrolysis Approach
por: Krupiński, Piotr, et al.
Publicado: (2022)