1
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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
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OpenAlex
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2
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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
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РИНЦ
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3
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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
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РИНЦ
OpenAlex
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4
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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
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РИНЦ
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5
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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
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РИНЦ
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6
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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
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РИНЦ
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7
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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
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РИНЦ
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8
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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
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РИНЦ
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9
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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
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РИНЦ
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10
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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
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РИНЦ
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11
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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
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РИНЦ
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12
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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
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РИНЦ
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13
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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
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РИНЦ
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14
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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
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РИНЦ
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15
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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
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РИНЦ
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16
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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
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РИНЦ
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17
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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
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РИНЦ
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18
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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.
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19
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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
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РИНЦ
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20
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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
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РИНЦ
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21
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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
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22
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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
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РИНЦ
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23
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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
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РИНЦ
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24
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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
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25
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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
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РИНЦ
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26
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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
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РИНЦ
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27
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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
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РИНЦ
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28
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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
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РИНЦ
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29
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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
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РИНЦ
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30
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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
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РИНЦ
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31
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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
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РИНЦ
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32
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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
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РИНЦ
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