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41
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Larin A.A.
, Ananyev I.V.
, Dubasova E.V.
, Teslenko F.E.
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, Khakimov D.V.
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Simple and energetic: Novel combination of furoxan and 1,2,4-triazole rings in the synthesis of energetic materials
Energetic Materials Frontiers. 2022.
V.3. N3. P.146-153. DOI: 10.1016/j.enmf.2022.08.002
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42
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Izmest'ev A.N.
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, Kravchenko A.N.
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5‐Indolylidene‐2‐iminothiazolidin‐4‐ones – Convenient Starting Compounds for Stereoselective Synthesis of Novel Dispirooxindole Derivatives
ChemistrySelect. 2022.
V.7. N2. e202104128
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43
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Kuptsova A.O.
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Methods for substitution of the thioxo group with the oxo group in imidazolidine-2-thione derivatives
Russian Chemical Bulletin. 2022.
V.71. N5. P.885-904. DOI: 10.1007/s11172-022-3488-0
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44
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Izmest’ev A.N.
, Streltsov A.А.
, Kravchenko A.N.
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The Chemo- and Regioselectivity of the Cyclization of Thiosemicarbazides with Haloacetic Acids and their Derivatives
Chemistry of Heterocyclic Compounds. 2022.
V.58. N10. P.483-492. DOI: 10.1007/s10593-022-03117-3
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45
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Vinogradov D.B.
, Izmest’ev A.N.
, Kravchenko A.N.
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A regioselective synthesis of imidazothiazolotriazines based on the cyclization of imidazotriazinethiones with phenacyl bromides
Chemistry of Heterocyclic Compounds. 2022.
V.58. N10. P.524-530. DOI: 10.1007/s10593-022-03123-5
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46
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Serkov S.A.
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, Kostikova N.N.
, Fedorov A.E.
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Synthesis of S-substituted 5-sulfonylmethyl(ethyl)-1,3,4-thiadiazol-2-amines
Chemistry of Heterocyclic Compounds. 2022.
V.58. N10. P.514-517. DOI: 10.1007/s10593-022-03121-7
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47
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Izmest'ev A.N.
, Kravchenko A.N.
, Gazieva G.A.
Synthesis of 7-oxindolylidene-3a,9a-diphenylimidazothiazolo[2,3-c][1,2,4]triazines by skeletal rearrangement of their [3,2-b]-fused isomers
Mendeleev Communications. 2022.
V.32. N5. P.678-679. DOI: 10.1016/j.mencom.2022.09.037
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48
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Izmest’ev A.N.
, Kravchenko A.N.
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Synthesis and antiproliferative activity characterization of new imidazothiazolotriazine oxindolylidene derivatives containing various substituents in the oxindole ring
Chemistry of Heterocyclic Compounds. 2022.
V.58. N10. P.531-538. DOI: 10.1007/s10593-022-03125-3
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49
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Izmest'ev A.N.
, Gazieva G.A.
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, Karnoukhova V.A.
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Synthesis and evaluation of the antiproliferative activity of new heterylmethylidene derivatives of imidazothiazolotriazinones
New Journal of Chemistry. 2021.
V.45. N27. P.12271-12285. DOI: 10.1039/d1nj02163j
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50
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Serkov S.А.
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, Sigay N.V.
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, Volkhina T.N.
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Synthesis of 1,3-dialkyl-4-[(arylmethylidene)amino]glycolurils
Chemistry of Heterocyclic Compounds. 2021.
V.57. N6. P.646-655. DOI: 10.1007/s10593-021-02963-x
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51
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Vinogradova E.E.
, Gazieva G.A.
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Dimroth-type N/S-interchange of N-aminothioglycolurils in the synthesis of 2-hydrazonoimidazo[4,5-d]thiazolones
RSC Advances. 2021.
V.11. N45. P.28395-28400. DOI: 10.1039/d1ra05568b
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52
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Izmest’ev A.N.
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, Kolotyrkina N.G.
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Synthesis of functionalized imidazo[4,5-e]thiazolo[3,2-b]triazines by condensation of imidazo[4,5-e]triazinethiones with DMAD or DEAD and rearrangement to imidazo[4,5-e]thiazolo[2,3-c]triazines
Beilstein Journal of Organic Chemistry. 2021.
V.17. P.1141-1148. DOI: 10.3762/bjoc.17.87
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53
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Makhova N.N.
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, Gazieva G.A.
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, Kuznetsov V.V.
, Kravchenko A.N.
, Krayushkin M.M.
, Rakitin O.A.
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Progress in the chemistry of nitrogen-, oxygen- and sulfur-containing heterocyclic systems
Russian Chemical Reviews. 2020.
V.89. N1. P.55-124. DOI: 10.1070/rcr4914
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54
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Izmest’ev A.N.
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Regioselectivity of (3+2) cycloaddition of azomethine ylides to activated olefins in the synthesis of spiro[oxindole-3,2′-pyrrolidine] derivatives
Chemistry of Heterocyclic Compounds. 2020.
V.56. N3. P.255-264. DOI: 10.1007/s10593-020-02654-z
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55
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Anikina L.V.
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Nootropic activity of N-(2-acetylaminoethyl)glycolurils
Russian Chemical Bulletin. 2020.
V.69. N3. P.563-566. DOI: 10.1007/s11172-020-2799-2
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56
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Izmest'ev A.N.
, Gazieva G.A.
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Diastereodivergent synthesis of dispiroheterocyclic structures comprising pyrrolidinyloxindole and imidazothiazolotriazine moieties
Organic & Biomolecular Chemistry. 2020.
V.18. N35. P.6905-6911. DOI: 10.1039/d0ob01628d
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57
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Izmest’ev A.N.
, Gazieva G.A.
, Kolotyrkina N.G.
, Daeva E.D.
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Synthesis of 5-arylmethylidene-3-(arylmethylideneamino)thiazolidine-2,4-diones via triazine ring cleavage of tetrahydroimidazothiazolotriazinediones and their reactions with azomethine ylides
Chemistry of Heterocyclic Compounds. 2020.
V.56. N12. P.1569-1578. DOI: 10.1007/s10593-020-02851-w
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58
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Ivolgina V.A.
, Popov L.D.
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Protolytic and potential antithyroid properties of thioglycolurils and fused azolo-1,2,4-triazines
Russian Chemical Bulletin. 2020.
V.69. N11. P.2215-2221. DOI: 10.1007/s11172-020-3024-z
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59
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Vikrishchuk N.I.
, Tkachev V.V.
, Borodkin G.S.
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Synthesis of 1,2,4-triazolo[5′,1′:2,3][1,3]thiazino[6,5-b]indol-10(5H)-ones based on 2-chloro-1H-indole-3-carbaldehyde
Tetrahedron Letters. 2020.
V.61. N45. 152490
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60
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Shmatkova N.V.
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Composition and Structure of Complexes Formed in GeCl4–2-Hydroxybenzene(2-hydroxynaphthaline-1)carbaldehyde Isonicotinoylhydrazone–ZnCl2–Methanol
Russian Journal of General Chemistry. 2020.
V.90. N12. P.2323-2327. DOI: 10.1134/s1070363220120154
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