A5110084090- Synthetic Organic Chemistry Methods
- Organometallic Complex Synthesis and Catalysis
- Advanced Polymer Synthesis and Characterization
- Synthesis and properties of polymers
- Chemical Synthesis and Analysis
- biodegradable polymer synthesis and properties
- Alzheimer's disease research and treatments
- Membrane Separation and Gas Transport
- Antimicrobial agents and applications
- Carbon dioxide utilization in catalysis
- Bacterial Infections and Vaccines
- RNA and protein synthesis mechanisms
- Coagulation, Bradykinin, Polyphosphates, and Angioedema
- Cell death mechanisms and regulation
- Asymmetric Hydrogenation and Catalysis
- Catalytic Cross-Coupling Reactions
- Click Chemistry and Applications
- Photopolymerization techniques and applications
- Biochemical effects in animals
- Advanced Glycation End Products research
- Molecular Spectroscopy and Structure
- Bacterial biofilms and quorum sensing
- Muon and positron interactions and applications
- Organic Chemistry Cycloaddition Reactions
- RNA Interference and Gene Delivery
Russian Academy of Sciences
2014-2025
A.V. Topchiev Institute of Petrochemical Synthesis
2014-2025
Institute of Bioorganic Chemistry
2007-2020
Institute of Bioorganic Chemistry
1976-2010
Friedrich Schiller University Jena
1991
Institute of Chemistry of High-Purity Substances them. G.G.Devyatyh
1985-1989
Institut für Medizinische Informatik, Biometrie und Epidemiologie
1977
State Research Institute for Chemistry and Technology of Organoelement Compounds
1966
A. N. Nesmeyanov Institute of Organoelement Compounds
1966
A series of antimicrobial protonated diallylammonium polymers, poly(diallylammonium trifluoroacetate) (PDAATFA), were synthesized by classical polymerization, using an especially elaborated method for preparation polymers with low molecular weight (MW), and RAFT different end groups in a range MW values (8–43) × 103 g∙mol−1. Cytotoxicity relative to eukaryotic cells (epithelioid lines A-549 MA-104) bactericidal activity the (relative Pseudomonas aeruginosa Staphylococcus aureus) are...
Abstract An efficient grafting‐onto way to polyoctenamer‐ graft ‐polyethylene glycol brushes is proposed, based on the combination of ring‐opening metathesis polymerization and polymer‐analogous reaction. New monomers cyclooct‐4‐en‐1‐ylmethyl methanesulfonate 4‐methylbenzenesulfonate are synthesized from cyclooctadiene then polymerized with high yields first generation Grubbs’ catalyst. Mesylate tosylate pendants in resulting polymers readily substituted oligoethylene monomethyl ethers...
ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXT6-Glycine-8-phenyllactic Acid Bradykinin. Its Synthesis, Biological Activity, and Splitting by Kininase (Carboxypeptidase N)G. A. Ravdel, M. P. Filatova, L. Shchukina, T. S. Paskhina, Surovikina, Trapeznikova, EgorovaCite this: J. Med. Chem. 1967, 10, 2, 242–246Publication Date (Print):March 1, 1967Publication History Published online1 May 2002Published inissue 1 March...
Abstract In the present study, macromolecular chain composition of copolymers prepared by reactive blending poly(ethylene terephthalate) (PET) and bisphenol A polycarbonate (PC) in presence Ti(OBu) 4 catalyst was tested using 1 H 13 C NMR spectroscopy. The spectra were meticulously analyzed across all regions, revealing unexpected results that provide new insights into transreaction mechanism occurring between these two polymers melt phase. It found only primary reactions occurred: formation...
A series of novel copolyesters based on polyethylene terephthalate (PET) and 4′-hydroxy-biphenyl-4-carboxylic acid (HBCA) was obtained by melt polycondensation bis(2-hydroxyethyl) 4′-acetoxybiphenyl-4-carboxylic (ABCA) as co-monomers with Sb2O3 a catalyst. Using this synthetic procedure, set copolymers containing 20–80 mol% HBCA units prepared. According to NMR spectroscopy, the were random composition. Copolyesters comprising 60–80 possessed increased heat resistance formed nematic melts at...