Applied Organometallic Chemistry
A highly sensitive chemosensor based on a metal‐organic framework for determining zinc ions in cosmetics creams and wastewater
Applied Organometallic Chemistry, Volume 38, Issue 5, May 2024.
Applied Organometallic Chemistry
Copper (II)‐azo sulfathiazole complex immobilized on UiO‐66‐NH2 (MOF) as a catalyst for the one‐pot synthesis of spiroindole‐pyranopyrazoles
Applied Organometallic Chemistry, Volume 38, Issue 5, May 2024.
ChemSusChem
Advances in the Stability of Catalysts for Electroreduction of CO2 to Formic Acid
ChemSusChem, Volume 17, Issue 14, July 22, 2024.
ChemCatChem
Dehydrogenative Oxidation of Alcohols by Reusable Iridium Catalysts with a Cooperative Polymer Ligand
ChemCatChem, Volume 16, Issue 16, August 26, 2024.
Environmental Toxicology and Chemistry
Novel Reproduction Toxicity Test Method for Hyalella azteca Using Sexually Mature Amphipods Provides More Robust Data Than Standard Methods in Exposures to Imidacloprid
Environmental Toxicology and Chemistry, Volume 43, Issue 4, Page 723-735, April 2024.
Environmental Toxicology and Chemistry
Nondestructive Evaluation of Metal Bioaccumulation and Biochemical Biomarkers in Blood of Broad‐Snouted Caiman (Caiman latirostris) from Northeastern Brasil
Environmental Toxicology and Chemistry, Volume 43, Issue 4, Page 878-895, April 2024.
Environmental Toxicology and Chemistry
An Integrated Metabolomics‐Based Model, and Identification of Potential Biomarkers, of Perfluorooctane Sulfonic Acid Toxicity in Zebrafish Embryos
Environmental Toxicology and Chemistry, Volume 43, Issue 4, Page 896-914, April 2024.
Chemistry & Biodiversity
Anti‐inflammatory Polyketides from an Endophytic Fungus Chaetomium sp. UJN‐EF006 of Vaccinium bracteatum
Chemistry &Biodiversity, Volume 21, Issue 4, April 2024.
Applied Organometallic Chemistry
Improving the anticancer activity of fluorinated glucosamine and galactosamine analogs by attachment of a ferrocene or ruthenium tetrazene motif
Applied Organometallic Chemistry, Volume 38, Issue 5, May 2024.
Synlett
Manganese(I)-Catalyzed C–H Allylation of Tryptophans and Their Oligopeptides On Water
The manganese(I)-catalyzed allylation of the amino acid tryptophan is realized under exceedingly mild conditions using water as a sustainable and non-hazardous reaction medium, instead of classical organic solvents, with great potential for green and sustainable chemistry. Synthetically useful α,β-unsaturated esters can be accessed by reaction with Morita–Baylis–Hillman (MBH) adducts following a fast C–H activation approach. The robustness of this procedure is reflected by kinetic analysis at different reaction temperatures and reduced catalyst loadings are employed.