Results 161 to 170 of about 81,237 (352)

Nitrogen‐Rich, Tröger's Base‐Linked Porous Organic Polymers (POPs) as Heterogeneous Catalysts and Adsorbents of Organic Pollutants From Water

open access: yesJournal of Applied Polymer Science, Volume 143, Issue 3, January 15, 2026.
Synthesized Tröger's based POPs showed great versatility in heterogeneous catalysis reactions and for pollutant adsorption. ABSTRACT Porous organic polymers are a new class of polymeric materials that combine permanent porosity, high surface area, monomer diversity, and synthetic tunability, making them highly promising candidates for application in ...
Tiago F. Machado   +4 more
wiley   +1 more source

Highly Efficient Organocatalytic House‐Meinwald Rearrangement for the Facile Synthesis of Aldehydes: Swift Access to Ibuprofen

open access: yesChemistry – A European Journal, Volume 32, Issue 2, 9 January 2026.
We use readily available epoxides and 0.5 mol% bis(trifluoromethane)sulfonimide (Tf2N) as a catalyst to synthesize a broad range of aldehydes in yields ranging from 89% to 97%. Furthermore, we identified aldehyde dimerization intermediates at lower temperatures and observed their cleavage at 55 °C.
Friedemann Dressler   +3 more
wiley   +1 more source

Structure–Activity Relationship of Pyrrolidine Pentamine Derivatives as Inhibitors of the Aminoglycoside 6′-N-Acetyltransferase Type Ib [PDF]

open access: gold
Jan Sklenicka   +12 more
openalex   +1 more source

Synthesis of Functionalized Homoallylic Alcohols via a Salt‐Free Three‐Component Nickel‐Catalyzed Coupling Reaction

open access: yesAdvanced Synthesis &Catalysis, Volume 368, Issue 2, January 2026.
A nickel catalyzed three‐component coupling reaction between an aldehyde, a secondary amine, and butadiene allows a straightforward access to 5‐aminopent‐3‐en‐1‐ol scaffolds according to a salt‐free process. Key steps are oxidative coupling reaction between one aldehyde, one butadiene on a low valent nickel precursor, and the nucleophilic attack of a ...
Anthony Saint Pol   +8 more
wiley   +1 more source

Bicyclic Pyrrolidine Inhibitors of Toxoplasma gondii Phenylalanine t-RNA Synthetase with Antiparasitic Potency In Vitro and Brain Exposure [PDF]

open access: green
Chloe C. Ence   +11 more
openalex   +1 more source

Novel C20 Conjugated Fatty Acids as Biohydrogenation Intermediates in Paraclostridium bifermentans

open access: yesJournal of the American Oil Chemists' Society, Volume 103, Issue 1, Page 27-34, January 2026.
ABSTRACT In this paper, we report a detailed characterization of the eicosapentaenoic acid (EPA) hydrogenation pathway in Paraclostridium bifermentans JCM 1386T, including the identification of novel intermediates of conjugated EPAs, cis‐5,cis‐8,cis‐11,trans‐13,cis‐17‐20:5 (CEPA1) and cis‐5,cis‐8,trans‐11,trans‐13,cis‐17‐20:5 (CEPA2) by nuclear ...
Juo‐Ying Chen   +7 more
wiley   +1 more source

The Chemistry of Subphthalocyanines: Synthetic Strategies for their Axial, Peripheral, and Remote Postfunctionalization

open access: yesChemistryEurope, Volume 4, Issue 1, January 2026.
From axial and peripheral reactivity to remote derivatization, the chemical versatility of subphthalocyanines (SubPcs) renders them ideal scaffolds for the design of advanced functional materials. This review assembles the synthetic toolbox, key reaction conditions, and future challenges in SubPc functionalization, guiding the development of next ...
Marta Gómez‐Gómez   +4 more
wiley   +1 more source

Imidazoline‐Proline and Imidazoline‐Prolinate Ligands for Copper‐Catalyzed Asymmetric Exo‐Selective [3 + 2] Cycloaddition of Iminoesters with Nitroalkenes

open access: yesChemistryEurope, Volume 4, Issue 1, January 2026.
From a modular synthesis of nonphosphine chiral nitrogen‐based chiral imidazoline–amino acid ligands, two new chiral imidazoline–proline‐copper catalysts are developed for targeting exo‐selective [3 + 2] cycloaddition reaction. Density functional theory studies rationalize the observed stereoselectivity and the distinct chiral pockets of the two ...
Yan Yu   +4 more
wiley   +1 more source

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