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Articles (49) More info
1 |
Akulov A.A.
, Varaksin M.V.
, Nelyubina A.A.
, Tsmokaluk A.N.
, Mazhukin D.G.
, Tikhonov A.Y.
, Charushin V.N.
, Chupakhin O.N.
Iodine-Catalyzed Radical C–H Amination of Nonaromatic Imidazole Oxides: Access to Cyclic α-Aminonitrones Journal of Organic Chemistry. 2024. V.89. N1. P.463-473. DOI: 10.1021/acs.joc.3c02230 WOS Scopus |
2 |
Nikiforov E.A.
, Vaskina N.F.
, Moseev T.D.
, Varaksin M.V.
, Butorin I.I.
, Melekhin V.V.
, Tokhtueva M.D.
, Mazhukin D.G.
, Tikhonov A.Y.
, Charushin V.N.
, Chupakhin O.N.
Indolyl-Derived 4H-Imidazoles: PASE Synthesis, Molecular Docking and In Vitro Cytotoxicity Assay Processes. 2023. V.11. N3. P.846. DOI: 10.3390/pr11030846 WOS Scopus РИНЦ |
3 |
Uchida Y.
, Sakaguchi T.
, Oki S.
, Shimono S.
, Park J.
, Sugiyama M.
, Sato S.
, Zaytseva E.
, Mazhukin D.G.
, Tamura R.
Magnetically Manipulable Ionic Liquid Crystals Incorporating Neutral Radical Moiety ChemPlusChem. 2022. e202100352 . DOI: 10.1002/cplu.202100352 WOS Scopus РИНЦ |
4 |
Kirilyuk I.A.
, Mazhukin D.G.
Chapter 2 General Approaches to Synthesis of NitroxidesGeneral Approaches to Synthesis of Nitroxides Monography chapter Nitroxides: Synthesis, Properties and Applications. – Royal Society of Chemistry., 2021. – C.7-70. – ISBN 9781788017527. DOI: 10.1039/9781788019651-00007 |
5 |
Zaytseva E.V.
, Mazhukin D.G.
Spirocyclic Nitroxides as Versatile Tools in Modern Natural Sciences: From Synthesis to Applications. Part I. Old and New Synthetic Approaches to Spirocyclic Nitroxyl Radicals Molecules. 2021. V.26. N3. 677 . DOI: 10.3390/molecules26030677 WOS Scopus |
6 |
Grigor'eva L.N.
, Tikhonov A.Y.
, Lomanovich K.A.
, Mazhukin D.G.
Stable Bicyclic Functionalized Nitroxides: The Synthesis of Derivatives of Aza-nortropinone-5-Methyl-3-oxo-6,8-diazabicyclo[3.2.1]-6-octene 8-oxyls Molecules. 2021. V.26. N10. 3050 . DOI: 10.3390/molecules26103050 WOS Scopus РИНЦ |
7 |
Amitina S.A.
, Zaytseva E.V.
, Dmitrieva N.A.
, Lomanovich A.V.
, Kandalintseva N.V.
, Ten Y.A.
, Artamonov I.A.
, Markov A.F.
, Mazhukin D.G.
5-Aryl-2-(3,5-dialkyl-4-hydroxyphenyl)-4,4-dimethyl-4H-imidazole 3-Oxides and Their Redox Species: How Antioxidant Activity of 1-Hydroxy-2,5-dihydro-1H-imidazoles Correlates with the Stability of Hybrid Phenoxyl-Nitroxides Molecules. 2020. V.25. N14. 3118 . DOI: 10.3390/molecules25143118 WOS Scopus |
8 |
Zaytseva E.
, Shiomi D.
, Ten Y.
, Gatilov Y.V.
, Lomanovich A.
, Stass D.
, Bogomyakov A.
, Yu A.
, Sugisaki K.
, Sato K.
, Takui T.
, Bagryanskaya E.
, Mazhukin D.
Magnetic Properties of Jr -Conjugated Hybrid Phenoxyl Nitroxide Radicals with Extended Jr-Spin Delocalization Journal of Physical Chemistry A. 2020. V.124. N12. P.2416-2426. DOI: 10.1021/acs.jpca.9b11856 WOS Scopus РИНЦ |
9 |
Zaytseva E.
, Timofeev I.
, Krumkacheva O.
, Parkhomenko D.
, Mazhukin D.
, Sato K.
, Matsuoka H.
, Takui T.
, Bagryanskaya E.
EPR and DEER Characterization of New Mixed Weakly Coupled Nitroxide Triradicals for Molecular Three-Spin Qubits Applied Magnetic Resonance. 2019. V.50. N8. P.967-976. DOI: 10.1007/s00723-019-01125-9 WOS Scopus РИНЦ |
10 |
Takemoto Y.
, Zaytseva E.
, Suzuki K.
, Yoshioka N.
, Takanishi Y.
, Funahashi M.
, Uchida Y.
, Akita T.
, Park J.
, Sato S.
, Clevers S.
, Coquerel G.
, Mazhukin D.G.
, Shimono S.
, Sugiyama M.
, Takahashi H.
, Yamauchi J.
, Tamura R.
Unique Superparamagnetic-like Behavior Observed in Non-pi-delocalized Nitroxide Diradical Compounds Showing Discotic Liquid Crystalline Phase Chemistry - A European Journal. 2018. V.24. N65. P.17293-17302. DOI: 10.1002/chem.201803534 WOS Scopus РИНЦ |
11 |
Zaytseva E.V.
, Gatilov Y.V.
, Mazhukin D.G.
The synthesis of new functionalized 1,3,5-triazine-based stable bi- and trinitroxides of the 2,5-dihydroimidazole series ARKIVOC. 2018. P.359-374. DOI: 10.24820/ark.5550190.p010.614 WOS Scopus РИНЦ |
12 |
Ten Y.A.
, Salnikov O.G.
, Amitina S.A.
, Stass D.V.
, Rybalova T.V.
, Kazantsev M.S.
, Bogomyakov A.S.
, Mostovich E.A.
, Mazhukin D.G.
The Suzuki-Miyaura reaction as a tool for modification of phenoxyl-nitroxyl radicals of the 4H-imidazole N-oxide series RSC Advances. 2018. V.8. N46. P.26099-26107. DOI: 10.1039/c8ra05103h WOS Scopus |
13 |
Chugunova E.
, Samsonov V.
, Akylbekov N.
, Mazhukin D.
Synthesis of 2H-benzimidazole 1,3-dioxides, separase inhibitors, by reaction of o-benzoquinone dioximes with ketones Tetrahedron. 2017. V.73. N27-28. P.3986-3992. DOI: 10.1016/j.tet.2017.05.078 WOS Scopus РИНЦ |
14 |
Suzuki K.
, Takemoto Y.
, Takaoka S.
, Taguchi K.
, Uchida Y.
, Mazhukin D.G.
, Grigor'ev I.A.
, Tamura R.
Chiral all-organic nitroxide biradical liquid crystals showing remarkably large positive magneto-LC effects Chemical Communications. 2016. V.52. N20. P.3935-3938. DOI: 10.1039/c5cc09202g WOS Scopus РИНЦ |
15 |
Tolstikov S.E.
, Tretyakov E.V.
, Gorbunov D.E.
, Zhurko I.F.
, Fedin M.V.
, Romanenko G.V.
, Bogomyakov A.S.
, Gritsan N.P.
, Mazhukin D.G.
Reaction of Paramagnetic Synthon, Lithiated 4,4,5,5-Tetramethyl-4,5-dihydro-1H-imidazol-1-oxyl 3-oxide, with Cyclic Aldonitrones of the Imidazole Series Chemistry - A European Journal. 2016. V.22. N41. P.14598-14604. DOI: 10.1002/chem.201602049 WOS Scopus РИНЦ |
16 |
Zaytseva E.V.
, Gatilov Y.V.
, Amitina S.A.
, Tamura R.
, Grigor'ev I.A.
, Mazhukin D.G.
Spirocyclic 2,5-dihydro-1H-imidazole 1-oxyl radicals with a mesogenic substituent on C-4. Synthesis and crystal structure Russian Journal of Organic Chemistry. 2014. V.50. N1. P.72-77. DOI: 10.1134/S107042801401014X WOS Scopus РИНЦ |
17 |
Bogdanova L.A.
, Morozkova T.S.
, Amitina S.A.
, Mazhukin D.G.
, Nikolin V.P.
, Popova N.A.
, Kaledin V.I.
Dual Effects of Indoleamine 2,3-Dioxygenase Inhibitors on the Therapeutic Effects of Cyclophosphamide and Cycloplatam on Ehrlich Ascites Tumor in Mice Bulletin of Experimental Biology and Medicine. 2014. V.157. N4. P.506-509. DOI: 10.1007/s10517-014-2602-1 WOS Scopus РИНЦ |
18 |
Zaytseva E.V.
, Shernyukov A.V.
, Genaev A.M.
, Tamura R.
, Grigor'ev I.A.
, Mazhukin D.G.
New spirocyclic nitroxides of 2,5-dihydroimidazole series flanked by two mesogenic fragments ARKIVOC. 2014. P.10-24. DOI: 10.3998/ark.5550190.p008.808 WOS Scopus РИНЦ |
19 |
Zaitseva E.V.
, Shernyukov A.V.
, Amitina S.A.
, Tamura R.
, Grigor'ev I.A.
, Mazhukin D.G.
Synthesis of Diastereomeric Spirocyclic Nitroxyl Radicals of 3-Imidazoline Series with Two Mesogenic Groups Chemistry of Heterocyclic Compounds. 2014. V.50. N8. P.1113-1125. DOI: 10.1007/s10593-014-1571-7 WOS Scopus РИНЦ |
20 |
Mostovich E.A.
, Mazhukin D.G.
, Rybalova T.V.
Reactions of vicinal aliphatic bis(hydroxylamines) with trifunctionalized methane derivatives ARKIVOC. 2011. P.29-42. DOI: 10.3998/ark.5550190.0012.b03 WOS Scopus РИНЦ |
21 |
Suzuki K.
, Mazhukin D.G.
, Takahashi H.
, Uchida Y.
, Tamura R.
, Grigor'ev I.A.
SYNTHESIS AND STEREOCHEMISTRY OF NOVEL RIGID NITROXIDE BIRADICALS BASED ON PARAMAGNETIC PYRROLIDINE CORE HETEROCYCLES. 2009. V.78. N12. P.3091-3099. DOI: 10.3987/COM-09-11821 WOS |
22 |
Mashevskaya I.V.
, Aliev Z.G.
, Mazhukin D.G.
, Popov S.A.
, Tikhonov A.Y.
, Maslivets A.N.
Five-membered 2,3-dioxo heterocycles: LXII. Reaction of 3-aroyl-1H-pyrrolo[2,1-c][1,4]benzoxazine-1,2,4-triones with N,N '-dihydroxycyclohexane-1,2-diamine. Unusual rearrangement in the spiro[quinoxaline-2,2 '-pyrrole] system Russian Journal of Organic Chemistry. 2008. V.44. N8. P.1189-1193. DOI: 10.1134/S1070428008080149 WOS Scopus РИНЦ |
23 |
Mostovich E.A.
, Mazhukin D.G.
, Gatilov Y.V.
, Rybalova T.V.
Coupling of 1,2-bis(alkoxyamino)cyclohexanes with 1,3-dicarbonyl compounds: first synthesis of 1,4-dialkoxy-2,3-dihydro-1,4-diazepinium salts Mendeleev Communications. 2007. V.17. N1. P.48-50. DOI: 10.1016/j.mencom.2007.01.019 WOS Scopus РИНЦ |
24 |
Keiko N.
, Funtilkova E.
, Larina L.
, Sarapulova G.
, Mazhukin A.
, Rybajova T.
, Tikhonov A.
Reaction of 2-alkoxypropenals with alpha-hydroxyamino oximes and 1,2-bis(hydroxyamino)cyclohexane Russian Journal of Organic Chemistry. 2005. V.41. N10. P.1421-1429. DOI: 10.1007/s11178-005-0361-1 WOS Scopus РИНЦ |
25 |
Butakov V.
, Khlestkin V.
, Mazhukin D.
Formation of N,N '-dihydroxy- and N,N '-dimethoxy-1,4-diazepine derivatives in the reaction of 1,2-bis(hydroxyamines) and 1,2-bis(methoxyamine) with enone Mannich bases Mendeleev Communications. 2005. V.15. N4. P.162-163. DOI: 10.1070/MC2005v015n04ABEH002131 WOS Scopus РИНЦ |
26 |
Reznikov V.
, Roshchupkina G.
, Mazhukin D.
, Petrov P.
, Popov S.
, Fokin S.
, Romanenko G.
, Rybalova T.
, Gatilov Y.
, Shvedenkov Y.
, Irtegova I.
, Shundrin L.
, Ovcharenko V.
A new class of enehydroxylamino ketones - (R)-2-(1-hydroxy-4,4,5,5-tetraalkylimidazolidin-2-ylidene)ethanones: Synthesis and reactions European Journal of Organic Chemistry. 2004. V.2004. N4. P.749-765. DOI: 10.1002/ejoc.200300536 WOS Scopus РИНЦ |
27 |
Khlestkin V.
, Mazhukin D.
Recent advances in the application of N,O-dialkylhydroxylamines in organic chemistry Current Organic Chemistry. 2003. V.7. N10. P.967-993. DOI: 10.2174/1385272033486639 WOS Scopus |
28 |
Yelinova V.I.
, Bobko A.A.
, Mazhukin D.G.
, Markel A.L.
, Khramtsov V.V.
New donors and acceptors of nitrogen oxide as potential therapeutic agents Russian Journal of Bioorganic Chemistry. 2003. V.29. N4. P.395-401. DOI: 10.1023/A:1024913620825 WOS Scopus РИНЦ |
29 |
Khlestkin V.K.
, Mazhukin D.G.
, Tikhonov A.Y.
, Rybalova T.V.
, Bagryanskaya I.Y.
, Gatilov Y.V.
Intramolecular cyclization of 1,2-bis(N-alkoxy-N-nitrosoamino)alkanes: A unique route to 4,5-dihydro-1,2,3-triazole 2-oxides Synthesis. 2000. N5. P.681-690. DOI: 10.1055/s-2000-6399 WOS Scopus РИНЦ |
30 |
Mazhukin D.G.
, Tikhonov A.Y.
, Reznikov V.A.
, Volodarsky L.B.
Formation of cyclic ketene N-hydroxyaminals, 2-acylmethylene-1-hydroxyimidazolidines, in the reaction of 1,2-bishydroxylamines with 1,3-ketoaldehydes Mendeleev Communications. 2000. V.10. N2. P.69-71. DOI: 10.1070/MC2000v010n02ABEH001231 WOS Scopus РИНЦ |
31 |
Tikhonov A.Y.
, Mazhukin D.G.
, Grigor'eva L.N.
, Khlestkin V.K.
, Voinova N.N.
, Syropyatov B.o.Y.
, Shirinkina S.S.
, Volodarsky L.B.
Synthesis and inhibitory effect on platelet aggregation and antihypertensive activity of 1-hydroxy-2,5-dihydro-1H-imidazole-2-carboxylic acid 3-oxides, 1,3-dihydroxyimidazolidine-2-carboxylic acids, and 1,4-dihydroxy-2,3-piperazinediones Archiv der Pharmazie. 1999. V.332. N9. P.305-308. DOI: 10.1002/(SICI)1521-4184(19999)332:9<305::AID-ARDP305>3.0.CO;2-2 WOS Scopus РИНЦ |
32 |
Kirilyuk I.A.
, Utepbergenov D.I.
, Mazhukin D.G.
, Fechner K.
, Mertsch K.
, Khramtsov V.V.
, Blasig I.E.
, Haseloff R.F.
Thiol-induced nitric oxide release from 3-halogeno-3,4-dihydrodiazete 1,2-dioxides Journal of Medicinal Chemistry. 1998. V.41. N7. P.1027-1033. DOI: 10.1021/jm960737s WOS Scopus РИНЦ |
33 |
Mazhukin D.G.
, Tikhonov A.Y.
, Petrenko O.P.
, Volodarsky L.B.
Unexpected formation of substituted furazano[3,4-d]pyridazine trioxide from alpha-hydroxylaminoaldoxime and its photochemical transformation to nitroxyl radical of pyrrolidine series Химия гетероциклических соединений/Khimiya Geterotsiklicheskikh Soedinenii. 1997. N3. P.403-405. WOS |
34 |
Mazhukin D.G.
, Tikhonov A.Y.
, Petrenko O.P.
, Volodarskii L.B.
Unexpected formation of a substituted furazano-[3,4-d]pyridazine trioxide from α-hydroxylamino-aldoxime and its photochemical conversion to a pyrrolidine nitroxyl radical Chemistry of Heterocyclic Compounds. 1997. V.33. N3. P.343-345. DOI: 10.1007/BF02253116 Scopus РИНЦ |
35 |
Ovcharenko V.
, Korobkov I.
, Fokin S.
, Burdukov A.
, Romanenko G.
, Ikorskii V.
, Pervukhina N.
, Mazhukin D.
, Rezntkov V.
Complexes with nitroxides containing different substituents in the α-position to N·-O group competition of basicity and sterical availability of the donor functions of nitroxides in metal complexes with sterically hindered imidazolines Molecular Crystals and Liquid Crystals Science and Technology Section A: Molecular Crystals and Liquid Crystals. 1997. V.305. P.311-320. DOI: 10.1080/10587259708045068 WOS Scopus |
36 |
Khlestkin V.K.
, Mazhukin D.G.
, Tikhonov A.Y.
, Bagryanskaya I.Y.
, Gatilov Y.V.
, Utepbergenov D.I.
, Khramtsov V.V.
, Volodarsky L.B.
Unexpected transformation of 1,2-bis(N-methoxy-N-nitrosoamino) cycloalkanes: First synthesis of 4,5-dihydro-1,2,3-triazole 2-oxides Tetrahedron Letters. 1996. V.37. N33. P.5997-6000. DOI: 10.1016/0040-4039(96)01258-0 WOS Scopus РИНЦ |
37 |
Mazhukin D.G.
, Khlestkin V.K.
, Tikhonov A.Y.
, Volodarsky L.B.
Synthesis of 1,2-bis(methoxyamino)cycloalkanes from alicyclic 1,2-bis(hydroxyamines) Russian Chemical Bulletin. 1996. V.45. N4. P.880-884. DOI: 10.1007/BF01431317 WOS Scopus РИНЦ |
38 |
Dultseva G.G.
, Skubnevskaya G.I.
, Tikhonov A.Y.
, Mazhukin D.G.
, Volodarsky L.V.
Derivatives of dihydropyrazine-1,4-dioxide, 3-imidazoline 3-oxide, and alpha-phenyl nitrones with functional groups as new spin traps in solution and in the gas phase Journal of Physical Chemistry. 1996. V.100. N44. P.17523-17527. DOI: 10.1021/jp960438e WOS Scopus РИНЦ |
39 |
Khlestkin V.K.
, Reznikov V.A.
, Mazhukin D.G.
, Tikhonov A.Y.
, Volodarsky L.B.
Reaction of N-(1-cyano-1-methylethyl)-α-phenylnitrone with phenyl-, 2-pyridyl- And 2-thienyl magnesium bromides: A new approach to alkylaromatic α-hydroxyaminoketones Mendeleev Communications. 1996. V.6. N5. P.202-203. DOI: 10.1070/MC1996v006n05ABEH000646 Scopus РИНЦ |
40 |
Khramtsov V.V.
, Utepbergenov D.I.
, Woldman Y.Y.
, Vlassenko L.P.
, Markel A.L.
, Kiriljuk I.A.
, Grigor'ev I.A.
, Mazhokin D.G.
, Tikhonov A.Y.
, Volodarsky L.B.
In vitro and in vivo studies of derivatives of 1,2-diazetine and nitronylnitroxide as donors and acceptors of nitric oxide Biochemistry (Moscow). 1996. V.61. N10. P.1223-1231. WOS Scopus РИНЦ |
41 |
Utepbergenov D.I.
, Khramtsov V.V.
, Vlassenko L.P.
, Markel A.L.
, Mazhukin D.G.
, Tikhonov A.Y.
, Volodarsky L.B.
KINETICS OF NITRIC-OXIDE LIBERATION BY 3,4-DIHYDRO-1,2-DIAZETE 1,2-DIOXIDES AND THEIR VASODILATORY PROPERTIES IN-VITRO AND IN-VIVO Biochemical and Biophysical Research Communications. 1995. V.214. N3. P.1023-1032. DOI: 10.1006/bbrc.1995.2388 WOS Scopus РИНЦ |
42 |
Mazhukin D.G.
, Tikhonov A.Y.
, Volodarsky L.B.
, Evlampieva N.P.
, Vetchinov V.P.
, Mamatyuk V.I.
SYNTHESIS OF INDENO[1,2-B]PYRAZINE N-OXIDES BY REACTION OF NINHYDRIN WITH 1,2-BISHYDROXYLAMINES Liebigs Annalen der Chemie. 1994. N10. P.983-987. WOS |
43 |
Mazhukin D.G.
, Tikhonov A.Y.
, Volodarsky L.B.
, Evlampieva N.P.
, Vetchinov V.P.
, Mamatyuk V.I.
Synthesis of Indeno[1,2‐b]pyrazine N‐Oxides by Reaction of Ninhydrin with 1,2‐Bishydroxylamines Liebigs Annalen der Chemie. 1994. V.1994. N10. P.983-987. DOI: 10.1002/jlac.199419941005 Scopus |
44 |
Mazhukin D.G.
, Tikhonov A.Y.
, Volodarsky L.B.
, Konovalova E.P.
INTERACTION OF 1,2-BISHYDROXYLAMINES WITH 1,2-DICARBONYL COMPOUNDS - PREPARATION AND PROPERTIES OF 2,3-DIHYDROPYRAZINE-1,4-DIOXIDES Химия гетероциклических соединений/Khimiya Geterotsiklicheskikh Soedinenii. 1993. N4. P.514-522. WOS |
45 |
Mazhukin D.G.
, Tikhonov A.Y.
, Volodarskii L.B.
, Konovalova E.P.
, Tikhonova L.A.
, Bagryanskaya I.Y.
, Gatilov Y.V.
SYNTHESIS OF ALIPHATIC 1,2-BISHYDROXYLAMINES FROM 1,3-DIHYDROXYIMIDAZOLIDINES - THE CRYSTAL-STRUCTURE OF 1,2-BISHYDROXYLAMINOCYCLOALKANES Russian Chemical Bulletin. 1993. V.42. N5. P.851-857. DOI: 10.1007/BF00698944 WOS Scopus РИНЦ |
46 |
Mazhukin D.G.
, Tikhonov A.Y.
, Volodarskii L.B.
, Konovalova E.P.
Interaction of 1,2-bishyroxylamines with 1,2-dicarbonyl compounds. Isolation and properties of 2,3-dihydropyrazine-1,4-dioxides Chemistry of Heterocyclic Compounds. 1993. V.29. N4. P.437-445. DOI: 10.1007/BF00529884 Scopus РИНЦ |
47 |
Mazhukin D.G.
, Volodarskii L.B.
, Tikhonova L.A.
, Tikhonov A.Y.
Synthesis of 3,4-Dihydro-1,2-diazete 1,2-Dioxides based on 1,2-Bishydroxylamines and 1,2-Nitroso Oxime Mendeleev Communications. 1992. V.2. N1. P.29-30. DOI: 10.1070/MC1992v002n01ABEH000111 WOS Scopus РИНЦ |
48 |
Dulepova N.V.
, Mazhukin D.G.
, Tikhonov A.Y.
, Volodarskii L.B.
FORMATION OF 2-IMIDAZOLINE DERIVATIVES BY INTERACTION OF 1,2-HYDROXYLAMINOOXIMES WITH PHENYLGLYOXALS AND METHYLGLYOXALS Химия гетероциклических соединений/Khimiya Geterotsiklicheskikh Soedinenii. 1986. N8. P.1060-1064. WOS |
49 |
Dulepova N.V.
, Mazhukin G.
, Tikhonov Y.
, Volodarskii B.
Formation of 2-imidazoline derivatives in the reaction of 1,2-hydroxyamino oximes with phenyl- and methylglyoxal Chemistry of Heterocyclic Compounds. 1986. V.22. N8. P.856-860. DOI: 10.1007/BF01175059 Scopus РИНЦ |
Identifiers
Scopus ID:
6602487018
, 57221956469
ORCID: 0000-0002-6915-6287
ResearcherID: A-9160-2010 , R-1502-2019
ORCID: 0000-0002-6915-6287
ResearcherID: A-9160-2010 , R-1502-2019