B. V. Lyalin, V. L. Sigacheva, V. A. Kokorekin, V. A. Petrosyan, “A new synthesis of azopyrazoles by oxidation of C-aminopyrazoles on a NiO(OH) electrode”, Mendeleev Commun., 25:6 (2015), 479–481
L. S. Konstantinova, S. A. Amelichev, S. G. Zlotin, M. I. Struchkova, T. I. Godovikova, O. A. Rakitin, “[1,4]Dithiino[2,3-c:5,6-c' ]bis[1,2,5]oxadiazole di-N-oxide: synthesis and oxidation to mono- and bis-S-oxides”, Mendeleev Commun., 25:5 (2015), 339–340
S. G. Zlotin, A. M. Churakov, O. A. Luk'yanov, N. N. Makhova, A. Yu. Sukhorukov, V. A. Tartakovsky, “Novel approaches to pharmacology-oriented and energy rich organic nitrogen–oxygen systems”, Mendeleev Commun., 25:6 (2015), 399–409
С. Г. Злотин, С. В. Кочетков, “$C_2$-симмeтpичныe диaмины и иx пpoизвoдныe – пepcпeктивныe opгaнoкaтaлизaтopы для acиммeтpичecкoгo cинтeзa”, Усп. хим., 84:11 (2015), 1077–1099 ; S. G. Zlotin, S. V. Kochetkov, “$C_2$-symmetric diamines and their derivatives as promising organocatalysts for asymmetric synthesis”, Russian Chem. Reviews, 84:11 (2015), 1077–1099
A. G. Gerbst, N. E. Ustyuzhanina, N. E. Nifantiev, “Computational study of the possible formation of the ternary complex between thrombin, antithrombin III and fucosylated chondroitin sulfates”, Mendeleev Commun., 25:6 (2015), 420–421
V. D. Gvozdev, K. N. Shavrin, M. P. Egorov, O. M. Nefedov, “One-pot synthesis of 1-arylmethylidene-1,2,3,3a-tetrahydro-5H-pyrrolo[1,2-a]-[3,1]benzoxazines and 1-arylmethylidene-1,2,3,3a,4,5-hexahydropyrrolo[1,2-a]-quinazolines from 5-arylalk-4-ynals and o-aminobenzylic alcohol/amine”, Mendeleev Commun., 25:5 (2015), 329–331
A. O. Chizhov, E. V. Sukhova, E. A. Khatuntseva, Yu. E. Tsvetkov, N. E. Nifantiev, “High-resolution mass spectra of biotinylated, HEG-spacered molecular probes with oligosaccharide fragments of the capsular polysaccharides from Streptococcus pneumoniae”, Mendeleev Commun., 25:6 (2015), 457–459
P. V. Markov, O. V. Turova, I. S. Mashkovsky, A. K. Khudorozhkov, V. I. Bukhtiyarov, A. Yu. Stakheev, “Size effect in the liquid phase semihydrogenation of substituted alkynes over supported Pd/Al2O3 catalysts”, Mendeleev Commun., 25:5 (2015), 367–369
М. Л. Генинг, Е. А. Курбатова, Ю. Е. Цветков, Н. Э. Нифантьев, “Paзpaбoткa пoдxoдoв к coздaнию yглeвoднoй кoнъюгиpoвaннoй вaкцины тpeтьeгo пoкoлeния пpoтив Streptococcus pneumoniae: пoиcк oптимaльныx oлигocaxapидныx лигaндoв”, Усп. хим., 84:11 (2015), 1100–1113 ; M. L. Gening, E. A. Kurbatova, Yu. E. Tsvetkov, N. E. Nifantiev, “Development of approaches to a third-generation carbohydrate-conjugate vaccine against Streptococcus pneumoniae: the search for optimal oligosaccharide ligands”, Russian Chem. Reviews, 84:11 (2015), 1100–1113
A. A. Zeifman, V. S. Stroylov, I. Yu. Titov, F. N. Novikov, O. V. Stroganov, I. Svitanko, G. G. Chilov, “Modeling of the Diels–Alder reaction enantioselectivity by quantum mechanics and molecular mechanics”, Mendeleev Commun., 25:4 (2015), 269–270
L. L. Fershtat, S. S. Ashirbaev, A. S. Kulikov, V. V. Kachala, N. N. Makhova, “Ionic liquid-mediated synthesis of (1H-1,2,3-triazol-1-yl)furoxans by [3 + 2] cycloaddition of azidofuroxans to acetylenes”, Mendeleev Commun., 25:4 (2015), 257–259