Results 311 to 320 of about 537,407 (394)

A Reexamination of CO2 Reduction with Fe2S2 Hydrogenase Mimics: Lessons in Using a Hydrogen Evolution Reaction Catalyst for CO2 to Formate Catalysis

open access: yesChemElectroChem, Volume 12, Issue 13, July 3, 2025.
Combining cyclic voltammetry, infrared spectroelectrochemistry, and density functional theory methods, the reduction of CO2 by an [FeFe] hydrogenase mimic was examined. Despite its ability to form stable reduced hydride species, this catalyst does not selectively reduce CO2 to HCOO− under the tested conditions.
Christopher J. Miller   +6 more
wiley   +1 more source

Alcohol and Carbonyl Redox Reactions in Electrochemical Organic Synthesis

open access: yesChemistryEurope, EarlyView.
This review aims to provide the reader with a useful tool to deal with electrochemical redox reactions involving alcohols and carbonyl compounds. The review is organized in an accessible format and divided into sections that focus on key parameters of wide‐ranging electrosynthetic methods.
Fiammetta Vitulano   +5 more
wiley   +1 more source

Development and validation of a risk prediction model for gastroesophageal reflux disease: Gastroesophageal Reflux Disease Risk Scoring System. [PDF]

open access: yesWorld J Gastrointest Pathophysiol
Subramanian S   +6 more
europepmc   +1 more source

Mono‐Ethyl‐Phosphonates: Functional Group Masking Strategy to Stabilize and Optimize the Pharmacokinetics of Rare Earth Radiochelates

open access: yesChemistryEurope, EarlyView.
Prodrug strategies are used to enhance the pharmacokinetics of small molecule drugs. Here, this approach to rare earth coordination complexes is adopted with applications as diagnostic and therapeutic radiopharmaceuticals: a mono‐ethyl‐phosphonate polyazamacrocyclic chelator for 44Sc and 177Lu reduces blood and bone uptake.
Jennifer N. Whetter   +8 more
wiley   +1 more source

Does Stapling Platform Influence Robotic Sleeve Gastrectomy Postoperative Outcomes? [PDF]

open access: yesObes Surg
Ying L   +5 more
europepmc   +1 more source

Synthetic Study on Bicyclic Pyranonaphthoquinone Natural Products: Construction of the Dioxabicyclo[3.3.1]nonene Motif

open access: yesChemistryEurope, EarlyView.
The method for the stereoselective formation of dioxabicyclo[3.3.1]nonene structure has been developed. The intriguing bicyclic skeleton is embedded in hybrid‐type pyranonaphthoquinone natural products, e.g., glenthamine Treatment of nanaomycin D and naphthol with Na2HPO4 in DMSO and water affords the bicyclic compound in good yield.
Yoshio Ando, Sota Ajima, Ken Ohmori
wiley   +1 more source

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