Results 21 to 30 of about 1,796 (140)

Redox‐Active Guanidines

open access: yesChemElectroChem, Volume 13, Issue 12, 17 June 2026.
Redox‐active guanidines, comprising guanidino‐functionalized aromatics (GFAs) and redox‐active urea azines (RAAs), are electron donors and strong Lewis and Brønsted bases that are used in several applications. They act as redox‐active ligands in bistable coordination compounds and as reagents in dehydrogenative coupling reactions and proton‐coupled ...
Hans‐Jörg Himmel
wiley   +1 more source

Emerging Trends in Organic Photoreactions Utilizing Disulfides

open access: yesEuropean Journal of Organic Chemistry, Volume 29, Issue 21, 4 June 2026.
Disulfides are versatile, nontoxic alternatives to metal photocatalysts. This review explores their role as photoactivated thiyl‐radical precursors and bifunctional catalysts (HAT/electron shuttling) in diverse transformations. Strategies for electronic tuning and development into recyclable heterogeneous materials are highlighted for sustainable ...
Sunil Kumar   +3 more
wiley   +1 more source

Direct Observation of Elusive (DTBM‐SEGPHOS)CuH Monomer Enables Mechanistic Insights Into Hydrocupration, Aggregation, and Dynamics of Alkene Functionalization Catalysis

open access: yesAngewandte Chemie Novit, Volume 2, Issue 2, June 2026.
The direct spectroscopic characterization of the elusive (DTBM‐SEGPHOS)CuH monomer enabled quantitative kinetic analysis to elucidate its stability, hydrocupration reactivity, and limitations in alkene functionalization catalysis. ABSTRACT The bulky diphosphine DTBM‐SEGPHOS is widely employed in CuH‐catalyzed transformations as it provides remarkably ...
David E. Ryan   +8 more
wiley   +1 more source

Constellation Plots in KNIME: An Automated Scaffold‐Based Workflow for Interactive Chemical Space Visualization

open access: yesMolecular Informatics, Volume 45, Issue 5, May 2026.
The interactive, automated scaffold‐based Constellation Plot workflow provides a high‐density visual representation of the chemical space of compound datasets with complex relationships. Chemical space analysis is extensively used in different chemistry areas, ranging from the study of natural products to drug discovery projects.
Carlos D. Ramírez‐Márquez   +2 more
wiley   +1 more source

Additives Promote Divergent Reactivity in Photolytic Deoxygenation and Lactonization Reactions of Cobalt Alkoxycarbonyls

open access: yesEuropean Journal of Organic Chemistry, Volume 29, Issue 14, 15 April 2026.
We report a carbonylation‐homolysis process to access acyl radicals that can undergo decarboxylation or cyclization onto tethered alkenes. In both cases, ligands and additives are shown to influence the outcome to give saturated or unsaturated products, in some cases with isomerization of the initial products.
Jacob N. Hackbarth   +4 more
wiley   +1 more source

Hypervalent Iodine‐Mediated Synthesis of Sulfones Using Organozinc Pivalates and Sulfinate Salts

open access: yesEuropean Journal of Organic Chemistry, Volume 29, Issue 13, 13 April 2026.
A general protocol for sulfone synthesis via sulfonyl‐containing hypervalent iodine reagents and organozinc pivalates is described. The method is practical, provides a broad scope of sulfone in moderate to high yield. bicyclo[1.1.1]pentane‐sulfones are also disclosed and a one‐pot synthesis of Diels–Alder adduct is presented. Sulfones are key motifs in
José C. Cunha   +4 more
wiley   +1 more source

A Review on Medicinal Chemistry and Biological Activity of Dihydropyrimidinones Against HIV

open access: yesArchiv der Pharmazie, Volume 359, Issue 4, April 2026.
This article presents the latest advances in the development of dihydropyrimidinone (DHPM) derivatives as promising candidates against HIV. By exploring their interactions with essential viral targets and highlighting innovative compounds with potent antiviral activity, we provide an updated perspective on the opportunities for new antiretroviral ...
Debora I. Leite   +11 more
wiley   +1 more source

Improved Process for the Continuous Acylation of 1,3-Benzodioxole

open access: yesMolecules
The acylation of 1,3-benzodioxole was studied in a continuous process using a recyclable heterogeneous substoichiometric catalyst. In a short time period (30 min), at 100 °C, the conversion rate was 73%, with a selectivity of 62% of the desired acylated product; the reaction was run continuously for 6 h, showing excellent stability and selectivity ...
Davide Pollon   +7 more
openaire   +5 more sources

BENZODIOXOLS FROM FERULA LAPIDOSA

open access: yesJournal of Research in Pharmacy, 2023
Kh. I. KHASANOVA   +2 more
openaire   +1 more source

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