Facile and economical Miyaura borylation and one-pot Suzuki–Miyaura cross-coupling reaction
Sign Up to like & getrecommendations! Published in 2020 at "Inorganica Chimica Acta"
DOI: 10.1016/j.ica.2020.119538
Abstract: Abstract Facile and economical method for Miyaura borylation reaction between B2pin2 and aryl bromides is reported. The catalytic system containing 2 mol% PdCl2(PPh3)2 and KOAc serves to enable borylations to occur under solvent-free and atmospheric conditions.… read more here.
Keywords: facile economical; miyaura borylation; reaction; one pot ... See more keywords
Synthesis and characterization of Pd-γ-Fe2O3 nanocomposite and its application as a magnetically recyclable catalyst in ligand-free Suzuki-Miyaura reaction in water
Sign Up to like & getrecommendations! Published in 2018 at "Journal of Organometallic Chemistry"
DOI: 10.1016/j.jorganchem.2018.06.016
Abstract: Abstract A novel redox-driven method to synthesize Pd-γ-Fe 2 O 3 nanocomposite from Fe 3 O 4 and PdCl 2 under modified hydrothermal technique has been developed. The synthesized nanocomposite was characterized by XRD, FT-IR,… read more here.
Keywords: fe2o3 nanocomposite; water; suzuki miyaura; characterization fe2o3 ... See more keywords
Highly Stereoselective Synthesis of Tetrasubstituted Acyclic All-Carbon Olefins via Enol Tosylation and Suzuki-Miyaura Coupling.
Sign Up to like & getrecommendations! Published in 2017 at "Journal of the American Chemical Society"
DOI: 10.1021/jacs.7b05071
Abstract: A highly stereocontrolled synthesis of tetrasubstituted acyclic all-carbon olefins has been developed via a stereoselective enolization and tosylate formation, followed by a palladium-catalyzed Suzuki-Miyaura cross-coupling of the tosylates and pinacol boronic esters in the presence… read more here.
Keywords: synthesis tetrasubstituted; miyaura coupling; tetrasubstituted acyclic; suzuki miyaura ... See more keywords
Base-Free Nickel-Catalysed DecarbonylativeSuzuki-Miyaura Coupling of Acid Fluorides
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DOI: 10.1038/s41586-018-0628-7
Abstract: The Suzuki–Miyaura cross-coupling of organoboron nucleophiles with aryl halide electrophiles is one of the most widely used carbon–carbon bond-forming reactions in organic and medicinal chemistry1,2. A key challenge associated with these transformations is that they… read more here.
Keywords: boronic acids; miyaura coupling; nickel catalysed; base ... See more keywords
Transition-Metal-Catalyzed Suzuki–Miyaura-Type Cross-Coupling Reactions of π-Activated Alcohols
Sign Up to like & getrecommendations! Published in 2020 at "Synthesis"
DOI: 10.1055/s-0039-1690740
Abstract: The Suzuki–Miyaura reaction is one of the most powerful tools for the formation of carbon–carbon bonds in organic synthesis. The utilization of alcohols in this powerful reaction is a challenging task. This short review covers… read more here.
Keywords: catalysis; miyaura type; suzuki miyaura; miyaura ... See more keywords