Resveratrol-Based Carbamates as Selective Butyrylcholinesterase Inhibitors: Design, Synthesis, Computational Study and Biometal Complexation Capability [PDF]
Mario Sviben +8 more
openalex +1 more source
Polyurethane-Based Electronic Packaging: The Characterization of Natural Aging over a Decade. [PDF]
Wei X, Li H, Zhou R, Xie C, Ning H.
europepmc +1 more source
Reactions and reactivity of allylic and benzylic carbamates.
Jeffrey Charles. Longley
openalex +1 more source
Predicting the Stability of Base‐mediated C─H Carboxylation Adducts Using Data Science Tools
A computational approach integrating quantum chemistry and machine learning enables the prediction of CO2–adduct stability. Model interpretability and experimental validation highlight its utility for designing base‐mediated C–H carboxylation reactions.
Maike Eckhoff +6 more
wiley +2 more sources
Climatic Conditions and Amine Loading Impact the Performance of Laminate-Supported Poly(ethylenimine) Direct Air Capture Sorbents. [PDF]
Ryu U +5 more
europepmc +1 more source
Total Synthesis of the Cyanobacterial Alkaloid Nostodione A
The total synthesis of the alkaloid nostodione A is successfully achieved utilizing 3,4‐dihydrocyclopenta[b]indole‐1,2‐dione as a key intermediate. The sensitive benzylidene moiety is introduced via a Knoevenagel condensation with p‐hydroxybenzaldehyde.
Oscar F. Casadiego‐Díaz +3 more
wiley +1 more source
Identification of Novel β-Lactam Derivatives as Proteasome Inhibitors for Antitumor Therapy. [PDF]
Cao Y +11 more
europepmc +1 more source
Electrochemical Intramolecular Aminobromination of Alkenes
A versatile electrochemical method for the intramolecular aminobromination of alkenes has been developed. The method provides access to five‐, six‐, and seven‐membered heterocycles by exploiting tetrabutylammonium bromide as an electrolyte and bromine source.
Sara Colombo +9 more
wiley +1 more source
Photolysis of ortho-Nitrobenzyl Esters: Kinetics and Substituent Effects. [PDF]
Fink AL, Groß AG, Puch F, Geitner R.
europepmc +1 more source

