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Suzuki–Miyaura cross coupling reaction: recent advancements in catalysis and organic synthesis

Brijesh S. Kadu
- 02 Mar 2021 - 
- Vol. 11, Iss: 4, pp 1186-1221
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TLDR
The advancements (within the last 4 years) in catalysis related to SMCR that would be beneficial for researchers in designing synthetic protocols for the preparation of pharmacophores as well as drug molecules are discussed.
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This article is published in Catalysis Science & Technology.The article was published on 2021-03-02. It has received 68 citations till now. The article focuses on the topics: Organic synthesis.

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Metal–Organic Framework: An Emergent Catalyst in C–N Cross-Coupling Reactions

TL;DR: In this paper , the state-of-the-art synthetic approaches for pristine and decorated metal-organic frameworks (MOFs) are comprehensively reviewed and discussed and forecast the future perspectives on MOFs catalyzed C-N cross-coupling reactions and associated challenges to establish the practical applicability of the catalyst at the industrial level.
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Access to chiral γ-butenolides via palladium-catalyzed asymmetric allylic C–H alkylation of 1,4-dienes

TL;DR: Asymmetric allylic C-H alkylation of 1,4-pentadienes with α-angelica lactones has been developed by tri-axial phosphoramidite-palladium catalysis as mentioned in this paper.
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Ionic chitosan Schiff bases supported Pd(II) and Ru(II) complexes; production, characterization, and catalytic performance in Suzuki cross-coupling reactions.

TL;DR: In this article, the authors developed new scaffolds (imidazolium-vanillyl-chitosan Schiff bases (IVCSSBs) for supporting Pd(II) and Ru(II)- ions in catalyzing Suzuki coupling reactions.
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Synthesis, crystal structure, spectral characterization, catalytic studies and computational studies of Ni(II) and Pd(II) complexes of symmetrical tetradentate Schiff base ligand

TL;DR: In this article , a symmetrical tetradentate Schiff base ligand (H2L) derived by the condensation of methoxy-salicylaldehyde with substituted phenylenediamine is used to prepare nickel (II) and palladium (II), and the chemical structures of the synthesized compounds were investigated with the help of combustion analysis and spectrophotometrically using FT-IR and 1H NMR.
References
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Journal ArticleDOI

Palladium-catalyzed cross-coupling reactions of organoboron compounds

Norio Miyaura, +1 more
- 01 Nov 1995 - 
TL;DR: In this paper, a cross-coupling reaction is proposed for coupling 1 -Alkenylboron Derivatives: Synthesis of Conjugated Dienes 6.
Journal ArticleDOI

Magnetic nanoparticles: Synthesis, protection, functionalization, and application

TL;DR: This review focuses on the synthesis, protection, functionalization, and application of magnetic nanoparticles, as well as the magnetic properties of nanostructured systems.
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Palladium(II)-catalyzed C-H activation/C-C cross-coupling reactions: versatility and practicality.

TL;DR: A review of palladium-catalyzed coupling of CH bonds with organometallic reagents through a PdII/Pd0 catalytic cycle can be found in this paper.
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A new stereospecific cross-coupling by the palladium-catalyzed reaction of 1-alkenylboranes with 1-alkenyl or 1-alkynyl halides

TL;DR: In this article, the representative (E)-1-alkenyldisiamylboranes and 1-alkenyl-1,3,2-benzodioxaboroles readily obtainable via hydroboration of 1 -alkynes react with (1) halides or (1)-alkynyl halides in the presence of a catalytic amount of tetrakis(triphenylphosphine)palladium and base to give corresponding conjugated (E-dienes or (E-)enynes with high regio-and
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Magnetic nanoparticles: design and characterization, toxicity and biocompatibility, pharmaceutical and biomedical applications.

TL;DR: Biocompatibility, Pharmaceutical and Biomedical Applications L. Harivardhan Reddy,‡ Jose ́ L. Arias, Julien Nicolas,† and Patrick Couvreur*,†.
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