Cargando…
Demonstration of Green Solvent Performance on O,S,N-Heterocycles Synthesis: Metal-Free Click Chemistry and Buchwald—Hartwig Coupling
The development of new and greener approaches to organic synthesis has been a trend in recent years. Continuing the latest publications of our team, in this work, we demonstrate the efficiency of three solvents: eucalyptol (1,8-cineole), cyclopentyl methyl ether (CPME), and 2-methyltetrahydrofuran (...
Autores principales: | Campos, Joana F., Cailler, Manon, Claudel, Remi, Prot, Benjamin, Besson, Thierry, Berteina-Raboin, Sabine |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7922032/ https://www.ncbi.nlm.nih.gov/pubmed/33670633 http://dx.doi.org/10.3390/molecules26041074 |
Ejemplares similares
-
Prediction of the Chemical Context for Buchwald‐Hartwig Coupling Reactions
por: Genheden, Samuel, et al.
Publicado: (2022) -
Buchwald–Hartwig
Amination of Aryl Halides
with Heterocyclic Amines in the Synthesis of Highly Fluorescent Benzodifuran-Based
Star-Shaped Organic Semiconductors
por: Bosiak, Mariusz J., et al.
Publicado: (2021) -
What can reaction databases teach us about Buchwald–Hartwig cross-couplings?
por: Fitzner, Martin, et al.
Publicado: (2020) -
The first Pd-catalyzed Buchwald–Hartwig aminations at C-2 or C-4 in the estrone series
por: Bacsa, Ildikó, et al.
Publicado: (2018) -
Solvent‐Free Synthesis of Core‐Functionalised Naphthalene Diimides by Using a Vibratory Ball Mill: Suzuki, Sonogashira and Buchwald–Hartwig Reactions
por: Panther, Lydia A., et al.
Publicado: (2022)