Results 131 to 140 of about 12,908,442 (282)
STUDY OF THE PROTONATION OF 1, 2, 4-TRIAZOLE. DFT CALCULATIONS
У цій роботі досліджена реакція між 1,2,4-тріазолом і хлоридною кислотою (HCl) з метою синтезу протонованого 1,2,4-тріазолу (TAH+). Ми використовували розрахунки теорії функціоналу густини (DFT), щоб отримати уявлення про структурний аналіз молекули. Кілька дескрипторів реакційної здатності, включаючи спорідненість до електрона, різниця енергій HOMO ...
El Addali, Abdelahad +4 more
openaire +2 more sources
A study of the inhibition of catalase by 3-amino-1:2:4-triazole [PDF]
E, MARGOLIASH, A, NOVOGRODSKY
openaire +2 more sources
[Cu(hyetrz)3](ClO4)2·3H2O (hyetrz = 4-(2-hydroxyethyl)-1,2,4-triazole) represents the first structurally characterized metal(II) chain compound containing triple N1,N2-1,2,4-triazole bridges. The structure has been solved at 298 K by single-crystal X-ray
Yann Garcia (1727962) +9 more
core +1 more source
Click chemistry has evolved from making covalent connections to also breaking bonds. Here, a cascade assembly is reported that combines these maneuvers to build multifunctional biomolecular scaffolds in a modular one‐pot reaction. The unifying azide release‐tetrazine hub clicks with a trans‐cyclooctene tag, rapidly liberates N,N‐dimethylaniline to ...
Markus Staudt +9 more
wiley +1 more source
This review critically evaluates clotrimazole as a potential antifungal for finfish aquaculture, highlighting strong mechanistic and in vitro efficacy against aquatic mycoses alongside major gaps in in vivo evidence, toxicokinetics, residue safety, and environmental risk, outlining priorities for responsible therapeutic development and regulatory ...
Arya Sen +2 more
wiley +1 more source
Mild C─F Activation of Azido(per)Fluoroalkanes
Mild and selective activation of C(sp3)–F bonds in azido(per)fluoroalkanes using thiolates was developed, leading to novel functionalized azides. The reaction is initiated by nucleophilic attack of the sulfur atom to the terminal nitrogen of the azido group, followed by fluoride ion elimination.
Olena Shaitanova +7 more
wiley +1 more source
Hybrid macrocyclic peptides unite genetically encoded peptide libraries with the structural complexity of synthetic small molecules. This Review critically analyzes phage‐compatible cyclization and diversification chemistries, highlights emerging opportunities beyond traditional cysteine‐based approaches, and outlines how future advances may enable the
Titia Rixt Oppewal, Clemens Mayer
wiley +1 more source
Chiral Pyrazolinylidene Complexes for Asymmetric Catalysis
The synthesis and application of pyrazolin‐5‐ylidene NHC chiral‐at‐ruthenium catalysts is reported. The strong donating pyrazolin‐5‐ylidene ligands led to highly electron rich ruthenium complexes, which showed excellent catalytic activity and enantioselectivity in the intramolecular aziridination of an alkene.
Felix Möller +6 more
wiley +1 more source
Design, Synthesis and Biophysical Characterisation of CPP-PNA Conjugates for Targeting Oncogenic microRNA-221. [PDF]
Cell‐penetrating peptide‐peptide nucleic acid (CPP‐PNA) conjugates that target the oncogenic microRNA‐221‐5p were synthesised using Cu(I)‐catalysed azide‐alkyne cycloaddition (CuAAC) and disulfide‐mediated conjugation strategies. These constructs form highly stable, sequence‐selective PNA/RNA heteroduplexes and demonstrate preliminary antiproliferative
Rotondo M +3 more
europepmc +2 more sources
Anion‐Selective Channels Formed by Synthetic 13‐Mer Chimeric α ‐Peptide‐Oligourea Foldamers
Synthetic 13‐mer α‐peptide‐oligourea chimeric foldamers self‐assemble into supramolecular ion channels, demonstrating high ion transport activity with distinct anion selectivity in lipid membranes. This study supports the design of bioinspired functional foldamer‐based channels for synthetic ion transport applications.
Chiranjit Dutta +10 more
wiley +1 more source

