Copper catalyzed carbon-selenium bond formation via the coupling reaction of aryl halides, phenylboronic acid and Se DOI Creative Commons

Zeinab Shirvandi,

Nadya Ghorashi,

Amin Rostami

и другие.

Scientific Reports, Год журнала: 2025, Номер 15(1)

Опубликована: Апрель 16, 2025

This is the first report for C-Se bond formation involving reaction of aryl halides with arylboronic acid and selenium powder to synthesis unsymmetrical diaryl selenides in presence CuI as a homogeneous catalyst. A wide range react various substituted groups under optimal conditions provide desired good high yields. Also, same reactions were investigated M-MCF@Gua-Cu reusable magnetic nanocatalyst conditions. The catalyst allows simpler (easy work-up) greener methodology. In addition, advantages presented method include use acid/Se safe cost-effective arylselenating system, simplicity operation, green cheap solvent.

Язык: Английский

Recent progress in copper-free Sonogashira-Hagihara cross-couplings in water DOI Creative Commons
Julia Struwe, Lutz Ackermann, Fabrice Gallou

и другие.

Chem Catalysis, Год журнала: 2022, Номер 3(1), С. 100485 - 100485

Опубликована: Дек. 22, 2022

Язык: Английский

Процитировано

26

Base metal chemistry and catalysis DOI Creative Commons
Marissa L. Clapson, Connor S. Durfy, Devon Facchinato

и другие.

Cell Reports Physical Science, Год журнала: 2023, Номер 4(9), С. 101548 - 101548

Опубликована: Авг. 21, 2023

This perspective provides an entry-level conversation concerning base metal catalysis as a green and sustainable solution in industrial academic contexts. We establish definition of "base metal," challenging readers to consider the ethical implications sourcing. explore what it means be "sustainable" provide information on current efforts synthetic chemistry. examples catalytic trends transformations popular fields such cross-coupling small-molecule conversion, highlighting relevant systems. Finally, we social context—for example, decisions related catalyst development are often driven by factors including costliness, safety, adoptability (whether society will accept its usage), performance. How do move forefront? Is concerned if materials fabricated from cheaper more abundant sources? does chemistry community guide this knowledge translation?

Язык: Английский

Процитировано

15

Applications of bio-resource based sustainable heterogeneous Pd-Nanocatalyst for Cross-Coupling and Michael addition reactions DOI Creative Commons
Md. Shaharul Islam, Shaheen M. Sarkar, Lutfor Rahman

и другие.

Chemical Engineering Journal, Год журнала: 2024, Номер 483, С. 149271 - 149271

Опубликована: Фев. 3, 2024

The development of efficient and cost-effective catalysts from renewable sources is crucial for sustainable chemistry. Herein, we developed a bio-heterogeneous Pd-nanocatalyst (PdNc@PA) by incorporating palladium nanoparticles into biodegradable kenaf-cellulose modified with poly(amidoxime) ligands. catalyst has demonstrated remarkable stability exceptional catalytic performance in range cross-coupling including Mizoroki-Heck, Suzuki-Miyaura, Tamejiro-Hiyama reactions inactivated aryl chlorides resulting high yields the desired coupling products. Additionally, PdNc@PA was also found to be effective Michael addition producing N, S, O-alkylated products yields. Furthermore, robustness recoverability allowing it reused across successive cycles without significant loss activity. incorporation resources offers an environmentally conscious alternative traditional synthetic approaches. This research highlights potential utilizing materials as supports, which could significantly diminish environmental impact waste production. Moreover, this study demonstrates versatility proficient reusable diverse array organic reactions. These discoveries provide encouraging pathway towards economically viable suitable industrial applications.

Язык: Английский

Процитировано

5

The sustainability impact of Nobel Prize Chemistry: life cycle assessment of C–C cross-coupling reactions DOI Creative Commons
José Luis Osorio-Tejada, Francesco Ferlin, Luigi Vaccaro

и другие.

Green Chemistry, Год журнала: 2023, Номер 25(23), С. 9760 - 9778

Опубликована: Янв. 1, 2023

Carbon-to-carbon (C–C) cross-coupling reaction (CCR) protocols represent a major breakthrough in synthetic chemistry.

Язык: Английский

Процитировано

13

Fibrous Material Structure Developments for Sustainable Heterogeneous Catalysis – An Overview DOI
Eva Loccufier, Damien P. Debecker, Dagmar D’hooge

и другие.

ChemCatChem, Год журнала: 2024, Номер 16(14)

Опубликована: Фев. 13, 2024

Abstract The continuous development of advanced catalysts to increase process yield and selectivity is crucial. A high specific surface area a good active phase dispersion are generally essential create catalytic materials with large number sites. Notably, fibrous morphology appealing because their surface‐to‐volume ratio flexibility. This contribution highlights the different types structures currently under investigation, all way from nanoscale macroscale back, where distinction lies in length diameter fibers, as well connection between structures. Fibers at least one submicron characteristic result higher yield, but can display practical usability issues when unbound. Therefore, structure balance small handleability important for industrial viability. By combining morphologies, best both nanomaterials macroscopic integer be combined into materials. overview showcases potential these makes clear that further research needed keep expanding use effectiveness catalysis.

Язык: Английский

Процитировано

5

GrafeoPlad Palladium: Insight on Structure and Activity of a New Catalyst Series of Broad Scope DOI Creative Commons
Matteo Formenti,

Maria Pia Casaletto,

Giampaolo Barone

и другие.

Advanced Sustainable Systems, Год журнала: 2024, Номер 8(4)

Опубликована: Март 17, 2024

Abstract GrafeoPlad‐Pd, a new metal‐organic alloy comprised of Pd nanoparticles doped with 3D‐entrapped graphene oxide, has promising applicative potential in sustainable synthetic organic chemistry. Besides hydrogenation, the metal nanopowder comprising material is also active and relatively stable cross‐coupling reactions carried out consecutively. X‐ray photoelectron spectroscopy (XPS) surface investigation density functional theory (DFT) calculations are applied to gain insight into structure catalytic activity this class molecularly metals.

Язык: Английский

Процитировано

4

Graphene loaded with metal nanoparticles/complexes catalyzed cross-coupling reactions: A review DOI
Maryam Mirza‐Aghayan,

Amir Sepehr Moieni,

Rabah Boukherroub

и другие.

Journal of Organometallic Chemistry, Год журнала: 2023, Номер 995, С. 122737 - 122737

Опубликована: Апрель 25, 2023

Язык: Английский

Процитировано

11

Nucleophilic addition of bulk chemicals with imines using N-functionalized hydroxylamine reagents as precursors DOI Creative Commons
Wei Wang, Yuanyuan Peng, Yang Liu

и другие.

Nature Communications, Год журнала: 2025, Номер 16(1)

Опубликована: Янв. 2, 2025

C–C and C–X bond forming reactions are essential tools in organic synthesis, constantly revolutionizing human life. Among the key methods for constructing new chemical bonds nucleophilic addition involving imines. However, inherent challenges synthesizing storing imines have stimulated interest designing stable precursors, which generates situ during reaction. This approach offers a promising alternative to traditional strategies holds significant potential future applications. Here we report direct general of with cost-effective feedstocks easily accessible nucleophiles, specifically utilizing N‑functionalized hydroxylamine reagents as bench-stable precursors. methodology streamlines synthesis various products, such amino acid derivatives, through wide range reaction types, including C–C, C–N, C–O, C–S constructions. Mechanistic studies DFT calculations provide insights into plausible mechanism that supports in-situ imine formation. The stimulate precursors can generate Here, authors N functionalized

Язык: Английский

Процитировано

0

Simultaneous Generation of Methyl Esters and CO in Lignin Transformation DOI
Mingyang Liu, Buxing Han, Paul J. Dyson

и другие.

Angewandte Chemie International Edition, Год журнала: 2022, Номер 61(40)

Опубликована: Авг. 18, 2022

Lignin is an abundant renewable carbon source. Due to its complex structure, utilization of lignin very challenging. Herein, we describe efficient strategy for the simultaneous lignin, in which methoxy groups react with carboxylic acids generate methyl carboxylates and other alkyl phenyl carbons oxygen predominantly form CO that can be used directly carbonylation reactions. The method was applied methylation various functionalized aryl acids, including natural compounds, produce valuable chemicals, pharmaceuticals. No solid or liquid residues remain after reaction. Mechanistic studies demonstrate a well-ordered C-C C-O bond activation sequence takes place realize total transformation lignin. This work opens way entire polymer into products, exemplified by synthesis pharmaceutical, Ramipril, on gram scale.

Язык: Английский

Процитировано

15

Recent advancements review Suzuki and Heck reactions catalyzed by metalloporphyrins DOI
Amir Mohammad Ghadiri,

Mehran Farhang,

Parya Hassani

и другие.

Inorganic Chemistry Communications, Год журнала: 2022, Номер 149, С. 110359 - 110359

Опубликована: Дек. 30, 2022

Язык: Английский

Процитировано

15