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41
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Muravyev N.V.
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V.24. N26. P.16325-16342. DOI: 10.1039/d1cp04663b
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42
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Khoranyan T.E.
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V.58. N1. P.37-44. DOI: 10.1007/s10593-022-03054-1
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43
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Suponitsky K.Y.
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Density Estimation Method for Individual Compounds from X-Ray Diffraction Analysis of their Solvated Forms
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V.58. N10. P.539-542. DOI: 10.1007/s10593-022-03126-2
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44
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Shkineva T.K.
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Synthesis of 2,5-disubstituted pyrazolyl-1,3,4-oxadiazoles by the Huisgen reaction
Russian Chemical Bulletin. 2022.
V.71. N8. P.1737-1744. DOI: 10.1007/s11172-022-3584-1
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45
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Gladyshkin A.G.
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Nitration of N-(fluorodinitroethyl)pyrazoles
Russian Chemical Bulletin. 2022.
V.71. N8. P.1701-1709. DOI: 10.1007/s11172-022-3580-5
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46
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Sinditskii V.P.
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Unique zwitterionic explosophore azasydnonimine: thermal stability, decomposition and combustion mechanism of aromatic derivatives
Journal of Thermal Analysis and Calorimetry. 2022.
V.147. N22. P.12871-12881. DOI: 10.1007/s10973-022-11503-4
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47
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Muravyev N.V.
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Chemical Engineering Journal. 2021.
V.421. 129804
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49
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FirePhysChem. 2021.
V.1. N2. P.83-89. DOI: 10.1016/j.fpc.2021.04.005
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Bastrakov M.A.
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V.57. N1. P.95-98. DOI: 10.1007/s10593-021-02873-y
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51
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Synthesis of 3(5)-aryl-5(3)-pyrazolyl-1,2,4-oxadiazole nitro derivatives
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V.57. N7-8. P.828-836. DOI: 10.1007/s10593-021-02987-3
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52
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Nazin G.M.
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V.15. N1. P.74-80. DOI: 10.1134/s1990793121010115
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Sinditskii V.P.
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Physical Chemistry Chemical Physics. 2021.
V.23. N20. P.11797-11806. DOI: 10.1039/d1cp01530c
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55
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V.89. N1. P.55-124. DOI: 10.1070/rcr4914
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V.32. N03. P.277-282. DOI: 10.1055/s-0040-1705960
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Pressure DSC for energetic materials. Part 2. Switching between evaporation and thermal decomposition of 3,5-dinitropyrazole
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58
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Dalinger I.L.
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Reactivity of Azasydnones: Unusual Diversity in Reactions of Chloro‐ and Nitrophenyl Derivatives with Nitrogen Nucleophiles
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V.9. N5. P.811-817. DOI: 10.1002/ajoc.201900757
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59
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Dalinger A.I.
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V.56. N2. P.180-191. DOI: 10.1007/s10593-020-02643-2
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V.4. N4. P.1510-1515. DOI: 10.1002/slct.201803068
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