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101.
We show that the structural properties of von Neumann algebra s are connected with the metric and order theoretic properties of various classes of affiliated subspaces. Among others we show that properly infinite von Neumann algebra s always admit an affiliated subspace for which (1) closed and orthogonally closed affiliated subspaces are different; (2) splitting and quasi‐splitting affiliated subspaces do not coincide. We provide an involved construction showing that concepts of splitting and quasi‐splitting subspaces are non‐equivalent in any GNS representation space arising from a faithful normal state on a Type I factor. We are putting together the theory of quasi‐splitting subspaces developed for inner product spaces on one side and the modular theory of von Neumann algebra s on the other side. 相似文献
102.
Nagaraju Chirra Varshitha Shanigarapu Naga Pranathi Abburi Ekaterina O. Sinegubova Ravi Kumar Pedapati Yana L. Esaulkova Vladimir V. Zarubaev Srinivas Kantevari 《Journal of heterocyclic chemistry》2024,61(3):496-505
Herein described the synthesis and antiviral evaluation of a novel series of morpholine and thio-morpholine coupled imidazo[2,1-b]thiazoles. The three-step reaction sequence involving the condensation of 1,3-dichloroacetone with thiourea followed by coupling with morpholine and thiomorpholine and finally cyclization with substituted α-bromoacetophenones yielded the desired imidazothiazoles 7(a–l) . Screening of all the new compounds for their in vitro antiviral activity against influenza virus A/Puerto Rico/8/34 (H1N1) in MDCK cells, resulted in two potent analogs, 7d (IC50: 1.1 μM, C50: >300 μM, SI = 273) and 7e (IC50: 2.0 μM, C50: >300 μM, SI = 150), with a favorable toxicity profile and are the best anti-influenza hit analogs for further structural optimization. 相似文献
103.
Nikita A. Kazin Nadezhda S. Demina Roman A. Irgashev Ekaterina F. Zhilina Gennady L. Rusinov 《Tetrahedron》2019,75(33):4686-4696
The effective approaches for regioselective double formylation and acetylation of 5,12-dialkyl-6,7-diaryl-substituted 5,12-dihydroindolo[3,2-a]carbazoles by their treatment with dichloromethyl methyl ether in the presence of SnCl4 or with acetyl chloride in the presence of AlCl3 to afford the 2,9-diformyl or 2,9-diacetyl derivatives, respectively, were developed. Furthermore, new 2,9-bis(2,2-dicyanovinyl) derivatives were synthesized by the Knoevenagel condensation of diformyl-containing substrates with malononitrile, when new 2,9-bis(quinoxaline-2-yl)- and 2,9-bis(benzo[g]quinoxaline-2-yl) derivatives were formed via microwave-promoted oxidation of diacetyl-containing substrates with SeO2 to the corresponding diglyoxals, followed by the reaction of these intermediates with o-phenylendiamine or 2,3-diaminonaphthalene, respectively. The basic optical and electrochemical properties of some 5,12-dihydroindolo[3,2-a]carbazoles were investigated. 相似文献
104.
A total synthesis of dioncoquinone B and related compounds, including ancistroquinones B, C and malvon A, is presented. The strategy is based on available reagents and can be used as a preparative synthesis of a number of natural and synthetic biologically active (3-alkyl)-2,7,8-di(tri)methoxy(hydroxy)-1,4-naphthoquinones. 相似文献
105.
Konstantin L. Ivanov Anna A. Kravtsova Elena A. Kirillova Mikhail Ya. Melnikov Ekaterina M. Budynina 《Tetrahedron letters》2019,60(30):1952-1955
A convenient synthetic strategy for the diastereoselective assembly of spiro[azepane-4,3′-oxindoles] was developed via a Staudinger/Michael/aza-Wittig/reduction/N-deprotection reaction sequence starting from PMB-protected oxindole-substituted ethylazides. The key step of the method is a domino self-catalytic Michael/aza-Wittig reaction wherein the phosphazene moiety acts first as the catalyst and then as the reactant, resulting in the formation of a seven-membered N-heterocycle. 相似文献
106.
Elizabeth Galati Huachen Tao Moritz Tebbe Rija Ansari Michael Rubinstein Ekaterina B. Zhulina Eugenia Kumacheva 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(10):3155-3159
Chiral packing of ligands on the surface of nanoparticles (NPs) is of fundamental and practical importance, as it determines how NPs interact with each other and with the molecular world. Herein, for gold nanorods (NRs) capped with end‐grafted nonchiral polymer ligands, we show a new mechanism of chiral surface patterning. Under poor solvency conditions, a smooth polymer layer segregates into helicoidally organized surface‐pinned micelles (patches). The helicoidal morphology is dictated by the polymer grafting density and the ratio of the polymer ligand length to nanorod radius. Outside this specific parameter space, a range of polymer surface structures was observed, including random, shish‐kebab, and hybrid patches, as well as a smooth polymer layer. We characterize polymer surface morphology by theoretical and experimental state diagrams. The helicoidally organized polymer patches on the NR surface can be used as a template for the helicoidal organization of other NPs, masked synthesis on the NR surface, as well as the exploration of new NP self‐assembly modes. 相似文献
107.
Daria D. Nedorezova Anna F. Fakhardo Daria V. Nemirich Ekaterina A. Bryushkova Dmitry M. Kolpashchikov 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(14):4702-4706
Despite decades of effort, gene therapy (GT) has failed to deliver clinically significant anticancer treatment, owing in part to low selectivity, low efficiency, and poor accessibility of folded RNA targets. Herein, we propose to solve these common problems of GT agents by using a DNA nanotechnology approach. We designed a deoxyribozyme‐based DNA machine that can i) recognize the sequence of a cancer biomarker with high selectivity, ii) tightly bind a structured fragment of a housekeeping gene mRNA, and iii) cleave it with efficiency greater than that of a traditional DZ‐based cleaving agent. An important advantage of the DNA nanomachine over other gene therapy approaches (antisense, siRNA, and CRISPR/cas) is its ability to cleave a housekeeping gene mRNA after being activated by a cancer marker RNA, which can potentially increase the efficiency of anticancer gene therapy. The DNA machine could become a prototype platform for a new type of anticancer GT agent. 相似文献
108.
Shakurova Elvira R. Salimova Elena V. Mescheryakova Ekaterina S. Parfenova Lyudmila V. 《Chemistry of Heterocyclic Compounds》2019,55(12):1204-1210
Chemistry of Heterocyclic Compounds - An efficient one-pot method was developed for the preparation of quaternary pyridinium salts and tetrahydropyridine derivatives of fusidane triterpenoids,... 相似文献
109.
Chi Zhang Ekaterina V. Vinogradova Alexander M. Spokoyny Stephen L. Buchwald Bradley L. Pentelute 《Angewandte Chemie (International ed. in English)》2019,58(15):4810-4839
Bioconjugation chemistry has been used to prepare modified biomolecules with functions beyond what nature intended. Central to these techniques is the development of highly efficient and selective bioconjugation reactions that operate under mild, biomolecule compatible conditions. Methods that form a nucleophile–sp2 carbon bond show promise for creating bioconjugates with new modifications, sometimes resulting in molecules with unparalleled functions. Here we outline and review sulfur, nitrogen, selenium, oxygen, and carbon arylative bioconjugation strategies and their applications to modify peptides, proteins, sugars, and nucleic acids 相似文献
110.
Azamat Temerdashev Ekaterina Dmitrieva Alice Azaryan Elina Gashimova 《Biomedical chromatography : BMC》2020,34(1):e4700
A simple and sensitive procedure for the quantification of two commonly abused aryl-propionamide-derived selective androgen receptor modulators (SARMs), namely S-4 (GTx-007, andarine) and S-22 (GTx-024, MK-2866, ostarine, enobosarm), has been described. Urine samples were prepared for analysis by means of a dispersive liquid–liquid microextraction using methanol and chloroform as dispersive and extracting solvents, respectively. Factors that might influence the extraction process as well as their optimum conditions were evaluated by Box–Benken and central composite designs. After extraction, the analytes were quantified by UHPLC–MS/MS. The proposed procedure was validated on human urine samples. As a result, for both SARMs the detection limits were observed at 0.05 ng/mL and calibration curves were linear in the concentration range of 0.25–50 ng/mL with the coefficient of determination of 0.998. 相似文献