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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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A Fluorescent Linear Conjugated Polymer Constructed from Pillararene and Anthracene

TL;DR: In this paper , a new luminescent linear conjugated polymers (CPs) was fabricated via the Sonogashira coupling of 9,10-diethynylanthracene and trifluoromethanesulfonic anhydride (OTf) modified pillar[5]arene, generating enhanced yellow-green fluorescence emission at around 552 nm.
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Monoribbed‐functionalized macrobicyclic iron( II ) complexes decorated with terminal reactive and vector groups: synthetic strategy towards, chemical transformations and structural characterization

TL;DR: In this article , a general and straightforward synthetic strategy towards the iron(II) clathrochelates with functionalizing substituents in their apical capping and one of the three chelate ribbed fragments was developed.
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Expanding the Synthetic Toolbox through Metal-Enzyme Cascade Reactions.

TL;DR: In this paper , a comprehensive review focusing on the period 2015 to early 2022, which has been divided into two main sections that comprise first the use of metals and enzymes as independent catalysts but working in an orchestral or sequential manner, and later their application as bionanohybrid materials through their coimmobilization in adequate supports.
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Palladium Supported on Bioinspired Materials as Catalysts for C–C Coupling Reactions

TL;DR: In this article , a review of biomaterials-supported metal catalysts applied to the formation of C-C bonds by Mizoroki-Heck, Suzuki-Miyaura and Sonogashira reactions is presented.
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
Journal ArticleDOI

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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