Научная деятельность
Статьи (38) Подробнее
1 |
Filippov I.R.
, Sonina A.A.
, Vorob’ev A.Y.
The synthesis of indolizin-1-ylphosphonates via the reaction of ethynylphosphonates with pyridinium methylides Chemistry of Heterocyclic Compounds. 2023. V.59. N11-12. P.786-792. DOI: 10.1007/s10593-024-03272-9 WOS РИНЦ |
2 |
Panfilov M.A.
, Karogodina T.Y.
, Sibiryakova A.A.
, Tretyakova I.S.
, Vorob'ev A.Y.
, Moskalensky A.E.
Meso-Aminomethyl-BODIPY as a Scaffold for Nitric Oxide Photo-Releasers ChemistrySelect. 2023. N8. P.46. DOI: 10.1002/slct.202302681 WOS РИНЦ |
3 |
Philippov I.
, Gatilov Y.
, Sonina A.
, Vorob’ev A.
Oxidative [3+2]Cycloaddition of Alkynylphosphonates with Heterocyclic N-Imines: Synthesis of Pyrazolo[1,5-a]Pyridine-3-phosphonates Molecules. 2022. V.27. N22. P.7913. DOI: 10.3390/molecules27227913 WOS РИНЦ |
4 |
Zobnina A.
, Moskalensky A.
, Vorob’ev A.
8‐[4‐(2‐hydroxypropane‐2‐yl)phenyl]‐1,3,4,4,5,7‐hexamethyl‐4‐ boron‐3a,4a‐diaza‐s‐indacene MolBank. 2021. V.2021. N4. M1286 . DOI: 10.3390/M1286 WOS Scopus РИНЦ |
5 |
Panfilov M.
, Chernova D.
, Khalfina I.
, Moskalensky A.
, Vorob’ev A.
Design and synthesis of new acridone-based nitric oxide fluorescent probe Molecules. 2021. V.26. N14. 4340 . DOI: 10.3390/molecules26144340 WOS Scopus РИНЦ |
6 |
Vorob′ev A.Y.
, Borodkin G.I.
, Andreev R.V.
, Shubin V.G.
1,3-Dipolar cycloaddition of cyanopyridines to heterocyclic N-imines: experimental and theoretical study Chemistry of Heterocyclic Compounds. 2021. V.57. N3. P.284-291. DOI: 10.1007/s10593-021-02905-7 WOS Scopus РИНЦ |
7 |
Dranova T.Y.
, Vorobev A.Y.
, Pisarev E.V.
, Moskalensky A.E.
Diaminorhodamine and Light-Activatable NO Donors: Photorelease Quantification and Potential Pitfalls Journal of Fluorescence. 2021. V.31. N1. P.11–16. DOI: 10.1007/s10895-020-02643-7 WOS Scopus РИНЦ |
8 |
Vorobev A.Y.
, Moskalensky A.E.
Long-wavelength photoremovable protecting groups: On the way to in vivo application Computational and Structural Biotechnology Journal. 2020. V.18. P.27-34. DOI: 10.1016/j.csbj.2019.11.007 WOS Scopus РИНЦ |
9 |
Chernova D.N.
, Sokolovski S.G.
, Vorobev A.Y.
, Moskalensky A.E.
Biophotonics approach for the study of leukocyte activation Progress in Biomedical Optics and Imaging - Proceedings of SPIE. 2020. V.11457. 114570G . DOI: 10.1117/12.2560325 WOS Scopus РИНЦ |
10 |
Spiryova D.V.
, Vorobev A.Y.
, Klimontov V.V.
, Koroleva E.A.
, Moskalensky A.E.
Optical uncaging of ADP reveals the early calcium dynamics in single, freely moving platelets Biomedical Optics Express. 2020. V.11. N6. P.3319-3329. DOI: 10.1364/BOE.392745 WOS Scopus РИНЦ |
11 |
Alieva S.V.
, Vorob’ev A.Y.
Synthesis of 3-Fluoropyrazolo[1,5-A]Pyridines by Fluorination of Methyl Pyrazolo[1,5-A]Pyridine-3-Carboxylates Chemistry of Heterocyclic Compounds. 2020. V.56. N7. P.957-960. DOI: 10.1007/s10593-020-02757-7 WOS Scopus РИНЦ |
12 |
Spiryova D.V.
, Vorob'ev A.Y.
, Moskalensky A.E.
Study of calcium signaling dynamics in single platelets using optical activation methods Proceedings of SPIE - The International Society for Optical Engineering. 2020. V.11359. 113590U . DOI: 10.1117/12.2559414 WOS Scopus РИНЦ |
13 |
Sannikova V.А.
, Filippov I.R.
, Karmatskikh O.Y.
, Panfilov M.А.
, Andreev R.V.
, Vorob’ev A.Y.
Synthesis of 3-and 2,3-substituted pyrazolo[1,5-a][1,10]phenanthrolines Chemistry of Heterocyclic Compounds. 2020. V.56. N8. P.1042-1047. DOI: 10.1007/s10593-020-02772-8 WOS Scopus РИНЦ |
14 |
Spiryova D.
, Vorob’ev A.
, Moskalensky A.E.
Оптическая стимуляция тромбоцитов двойным агонистом приводит к повышенной и надежной активации Proceedings of SPIE - The International Society for Optical Engineering. 2020. 9214621 :1-4. DOI: 10.1109/CSGB51356.2020.9214621 Scopus |
15 |
Vorob'ev A.Y.
Photocatalytic reaction of 4-cyanopyridine with tertiary amines Chemistry of Heterocyclic Compounds. 2019. V.55. N1. P.90-92. DOI: 10.1007/s10593-019-02423-7 WOS Scopus РИНЦ |
16 |
Evtushok V.E.
, Vorob'ev A.Y.
Synthesis of pyrazolo- and [1,2,4]triazolo-[1,5-a]quinolin-9-ols by cycloaddition to 8-hydroxyquinoline N-imide Chemistry of Heterocyclic Compounds. 2019. V.55. N3. P.229-234. DOI: 10.1007/s10593-019-02446-0 WOS Scopus РИНЦ |
17 |
Vorob'ev A.Y.
Methods of synthesis of [1,2,4]triazolo[1,5-a]pyridines (microreview) Chemistry of Heterocyclic Compounds. 2019. V.55. N8. P.695-697. DOI: 10.1007/s10593-019-02522-5 WOS Scopus РИНЦ |
18 |
Vorobi'ev A.Y.
, Dranova T.Y.
, Moskalensky A.E.
Photolysis of dimethoxynitrobenzyl-"caged" acids yields fluorescent products Scientific Reports. 2019. V.9. 13421 . DOI: 10.1038/s41598-019-49845-z WOS Scopus РИНЦ |
19 |
Moskalensky A.E.
, Spiryova D.V.
, Karmatskih O.Y.
, Vorobev A.Y.
MEASURING PLATELET ACTIVATION DYNAMICS USING OPTICALLY CONTROLLED AGONIST INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY. 2018. V.40. NSI. P.101. WOS |
20 |
Logutenko O.A.
, Titkov A.I.
, Vorob'ev A.M.
, Shundrina I.K.
, Yukhin Y.M.
, Lyakhov N.Z.
Synthesis of Nickel Nanoparticles by the Reduction of Its Salts Using the Modified Polyol Method in the Presence of Sodium Polyacrylates with Various Molecular Weights Russian Journal of General Chemistry. 2018. V.88. N2. P.288-294. DOI: 10.1134/S1070363218020160 WOS Scopus РИНЦ |
21 |
Логутенко О.А.
, Титков А.И.
, Воробьев А.Ю.
, Шундрина И.К.
, Юхин Ю.М.
, Ляхов Н.З.
СИНТЕЗ НАНОЧАСТИЦ НИКЕЛЯ ВОССТАНОВЛЕНИЕМ ЕГО СОЛЕЙ МОДИФИЦИРОВАННЫМ ПОЛИОЛЬНЫМ МЕТОДОМ В ПРИСУТСТВИИ ПОЛИАКРИЛАТОВ НАТРИЯ С РАЗЛИЧНОЙ МОЛЕКУЛЯРНОЙ МАССОЙ Журнал общей химии (RUSS J GEN CHEM+). 2018. Т.88. №2. С.311-318. РИНЦ |
22 |
Spiryova D.V.
, Karmatskih O.Y.
, Vorob'ev A.Y.
, Moskalensky A.E.
Towards optical control of single blood platelet activation Proceedings of SPIE - The International Society for Optical Engineering. 2018. V.10717. 1071722 . DOI: 10.1117/12.2305477 WOS Scopus РИНЦ |
23 |
Abramov P.A.
, Brylev K.A.
, Vorob'ev A.Y.
, Gatilov Y.V.
, Borodkin G.I.
, Kitamura N.
, Sokolov M.N.
Emission tuning in Re(I) complexes: Expanding heterocyclic ligands and/or introduction of perfluorinated ligands Polyhedron. 2017. V.137. P.231-237. DOI: 10.1016/j.poly.2017.08.046 WOS Scopus |
24 |
Vorob'ev A.Y.
, Supranovich V.I.
, Borodkin G.I.
, Shubin V.G.
New approach toward the synthesis of deuterated pyrazolo[1,5-a] pyridines and 1,2,4-triazolo[1,5-a] pyridines Beilstein Journal of Organic Chemistry. 2017. V.13. P.800-805. DOI: 10.3762/bjoc.13.80 WOS Scopus РИНЦ |
25 |
Romanov V.
, Vorob'ev A.
, Bagryanskaya I.
, Parkhomenko D.
, Tretyakov E.
1,3-Dipolar Cycloaddition of a Nitronyl Nitroxide-Substituted Alkyne to Heteroaromatic N-Imines Australian Journal of Chemistry. 2017. V.70. N12. P.1317-1320. DOI: 10.1071/CH17476 WOS Scopus РИНЦ |
26 |
Supranovich V.I.
, Vorob'ev A.Y.
, Borodkin G.I.
, Gatilov Y.V.
, Shubin V.G.
Study on selectivity in the reaction of 2-substituted pyridinium-N-imines with dimethyl acetylenedicarboxylate Tetrahedron Letters. 2016. V.57. N10. P.1093-1096. DOI: 10.1016/j.tetlet.2016.01.092 WOS РИНЦ |
27 |
Supranovich V.I.
, Borodkin G.I.
, Vorob'ev A.Y.
, Shubin V.G.
Unexpected cleavage of the C-py-C-py bond in the reaction of 2,2 '-bipyridine N,N '-diimines with acetylenes Tetrahedron Letters. 2014. V.55. N39. P.5377-5380. DOI: 10.1016/j.tetlet.2014.08.015 WOS Scopus РИНЦ |
28 |
Borodkin G.I.
, Vorob'ev A.Y.
, Supranovich V.I.
, Gatilov Y.V.
, Shubin V.G.
Molecular and crystal structure of 1,1 '-diamino-2,2 '-bipyridinium and 1,1 '-diamino-4,4 '-bipyridinium dimesitylenesulphonates: A combined experimental and theoretical study Journal of Molecular Structure. 2013. V.1035. P.441-447. DOI: 10.1016/j.molstruc.2012.11.043 WOS Scopus РИНЦ |
29 |
Borodkin G.I.
, Vorob'ev A.Y.
, Gatilov Y.V.
Molecular and crystal structure of (pyrazin-1-ium-1-yl)(perfluoropyridin-4-yl) and (4,4 '-bipyridin-1-ium-1-yl)(perfluoropyridin-4-yl)amides Journal of Structural Chemistry. 2012. V.53. N5. P.948-953. DOI: 10.1134/S0022476612050186 WOS Scopus РИНЦ |
30 |
Бородкин Г.И.
, Воробьев А.Ю.
, Гатилов Ю.В.
Молекулярная и кристаллическая структура (пиразиний-1)(перфторпиридин-4-ил) и (4,4′-бипиридилий)-1-ил(перфторпиридин-4-ил) амидов Журнал структурной химии (J STRUCT CHEM+). 2012. Т.53. №5. С.967-972. РИНЦ |
31 |
Бородкин Г.И.
, Воробьев А.Ю.
, Шубин В.Г.
Структурно-кинетические закономерности аминирования шестичленных n-гетероароматических соединений Журнал органической химии (RUSS J ORG CHEM+). 2011. Т.47. №6. С.21-22. РИНЦ |
32 |
Бородкин Г.И.
, Воробьев А.Ю.
, Шакиров М.М.
, Шубин В.Г.
О региоселективности аминирования азинов: взаимодействие производных пиразина с о-мезитиленсульфонилгидроксиламином Журнал органической химии (RUSS J ORG CHEM+). 2011. Т.47. №6. С.19-20. РИНЦ |
33 |
Borodkin G.I.
, Vorob'ev A.Y.
, Shakirov M.M.
, Shubin V.G.
Regioselectivity in the amination of azines: Reaction of pyrazine derivatives with O-mesitylenesulfonylhydroxylamine Russian Journal of Organic Chemistry. 2011. V.47. N6. P.889-896. DOI: 10.1134/S1070428011060108 WOS Scopus РИНЦ |
34 |
Borodkin G.I.
, Vorob'ev A.Y.
, Shubin V.G.
Structure-kinetics relations holding in the amination of six-membered nitrogen-containing heterocyclic compounds Russian Journal of Organic Chemistry. 2011. V.47. N6. P.897-903. DOI: 10.1134/S107042801106011X WOS Scopus РИНЦ |
35 |
Borodkin G.I.
, Vorob'ev A.Y.
, Shakirov M.M.
, Shubin V.G.
Regioselectivity in the amination of methylsulfanyl-substituted azines with O-mesitylenesulfonylhydroxylamine Russian Journal of Organic Chemistry. 2010. V.46. N6. P.911-916. DOI: 10.1134/S1070428010060229 WOS Scopus РИНЦ |
36 |
Borodkin G.I.
, Vorob'ev A.Y.
, Shakirov M.M.
, Shubin V.G.
Regioselectivity in 2-X-pyrazine aminations by O-mesitylenesulfonylhydroxylamine Tetrahedron Letters. 2009. V.50. N49. P.6779-6782. DOI: 10.1016/j.tetlet.2009.09.103 WOS Scopus РИНЦ |
37 |
Andreev R.V.
, Borodkin G.I.
, Vorob'ev A.Y.
, Gatilov Y.V.
, Shubin V.G.
Molecular and crystal structure of 1-amino-X-pyrazinium mesitylenesulfonates Russian Journal of Organic Chemistry. 2008. V.44. N2. P.292-301. DOI: 10.1134/S1070428008020188 WOS Scopus РИНЦ |
38 |
Андреев Р.В.
, Бородкин Г.И.
, Воробьев А.Ю.
, Гатилов Ю.В.
, Шубин В.Г.
Молекулярная и кристаллическая структура 1-амино-х-пиразиний мезитиленсульфонатов Журнал органической химии (RUSS J ORG CHEM+). 2008. Т.44. №2. С.296-304. РИНЦ |