Magnetite Pd-loaded nitrogen-rich porous organic polymer as a catalyst for suzuki-miyaura coupling reaction

Rahimi, Jamal; Naderi, Mehdi; Ijdani, Mohammad Tajik; Heidari, Marzieh; Azizi, Mojtaba; Maleki, Ali

doi:10.1016/j.mtchem.2023.101375

Cited by 7 publications

(9 citation statements)

References 34 publications

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“…The generation of Fe 3 O 4 NPs was processed using the typical co-precipitation technique according to the literature ( Rahimi et al, 2023 ). The obtained black precipitate was purified and neutralized with deionized water.…”

Section: Methodsmentioning

confidence: 99%

Melamine phosphate-modified magnetic chitosan: a novel biocompatible catalyst for the synthesis of biological tetrahydrodipyrazolopyridine and pyrazolopyranopyrimidine derivatives

Mousavi-Ebadi,

Safaei-Ghomi

2024

Front. Chem.

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A novel biocompatible composite was fabricated by the functionalization of magnetic chitosan with the melamine phosphate (MP) ionic compound to serve as a recoverable and bifunctional catalyst, aiming at the diversity-oriented generation of biological tetrahydropyrazolopyridine and pyrazolopyrimidine derivatives. This involved a meticulously orchestrated reaction, exploiting the in situ generated pyrazole alongside aromatic aldehydes, ammonium acetate, and (thio) barbituric acid. The present work manifests outstanding advantages, offering a novel and great method for the optimal synthesis of two valuable heterocyclic series especially five new derivatives. The resulting novel biocompatible composite was comprehensively characterized through a range of analytical techniques, including FT-IR, NH3 and CO2-TPD, XRD, TEM, FE-SEM, VSM, EDX, elemental CHNS analysis, ICP-MS, and NMR spectroscopy. Notably, the study represents a critical step in the preparation of advanced materials from accessible and cost-effective precursors.

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Section: Methodsmentioning

confidence: 99%

Melamine phosphate-modified magnetic chitosan: a novel biocompatible catalyst for the synthesis of biological tetrahydrodipyrazolopyridine and pyrazolopyranopyrimidine derivatives

Mousavi-Ebadi,

Safaei-Ghomi

2024

Front. Chem.

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“…[53][54][55][56][57] The catalytic applications of various forms of iron oxides and related hybrid catalysts are deliberated with emphasis on the non-magnetic supported or/iron oxides, especially hematite. The magnetically recyclable catalysts, [58][59][60][61][62][63][64][65] electrocatalysts, [66][67][68][69][70] and assorted Fenton-type reactions [71][72][73][74] associated with iron oxides are not included here as they have been well discussed in the literature and being beyond the scope of this review, with the exception of environmental applications. [75][76][77][78][79][80][81][82] Iron oxides are ideal oxide supports, as they are straightforward to synthesize, presence of highly reactive surface hydroxyl groups, facilitating effective adsorption and immobilization of metals and ligands.…”

Section: Catalytic Applications Of Nanosized Iron Oxidesmentioning

confidence: 99%

A review on sustainable iron oxide nanoparticles: syntheses and applications in organic catalysis and environmental remediation

Chaudhari,

Upadhyay,

Shinde

et al. 2024

Green Chem.

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“…Rahimi et al, [65] synthesized magnetic organic polymer-based nanoparticles and catalyzed the Suzuki-Miyaura coupling reaction (Scheme 37). The catalyst was synthesized using CC and diethylenetriamine in dioxane solvent under mild reaction conditions (Figure 5).…”

Section: Synthesis Of 14-dihydropyridines: Hantzsch Reactionmentioning

confidence: 99%

Role of cyanuric chloride in organic synthesis: A concise overview

Sethiya

Jangid

Pradhan

et al. 2023

Journal of Heterocyclic Chem

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Cyanuric chloride, a chlorinated analog of 1,3,5‐triazine, is used as a catalyst, promoter, and activator to catalyze and initiate several reactions like Beckmann rearrangement, Lossen rearrangement, Biginelli reaction, Suzuki coupling reaction, Pictet Spengler reaction, Mannich reaction, etc. It is employed in several reactions due to its several properties like stable, non‐volatile, cost‐efficient, easy to handle, and easy commercial availability. Moreover, it is a very renowned precursor for the synthesis of triazine‐class pesticide atrazine, dyes, and crosslinking agents. Herein in this review article, the reactions initiated, catalyzed, and promoted by cyanuric chloride from 2010 to 2022 have been elaborated.

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Magnetite Pd-loaded nitrogen-rich porous organic polymer as a catalyst for suzuki-miyaura coupling reaction

Cited by 7 publications

References 34 publications

Melamine phosphate-modified magnetic chitosan: a novel biocompatible catalyst for the synthesis of biological tetrahydrodipyrazolopyridine and pyrazolopyranopyrimidine derivatives

Melamine phosphate-modified magnetic chitosan: a novel biocompatible catalyst for the synthesis of biological tetrahydrodipyrazolopyridine and pyrazolopyranopyrimidine derivatives

A review on sustainable iron oxide nanoparticles: syntheses and applications in organic catalysis and environmental remediation

Role of cyanuric chloride in organic synthesis: A concise overview

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