TRANSFORMATION OF 2-METHYL-1-PHENYLETHYNYL-1,2,3,4-TETRAHYDROISOQUINOLINE BY THE ACTION OF ACTIVATED ALKYNES СтатьяVoskressensky L.G., Samavati R., Titov A.А., Alexandrova E.V., Chernikova N.Y., Varlamov A.V.Chemistry of Heterocyclic Compounds. Том 54. 2018. С. 576-580
ALCOHOL-INITIATED DINITRILE CYCLIZATION IN BASIC MEDIA: A ROUTE TOWARD PYRAZINO[1,2- A ]INDOLE-3-AMINES СтатьяFesta A.A., Golantsov N.E., Storozhenko O.A., Shumsky A.N., Varlamov A.V., Voskressensky L.G.Synlett. Том 29. 2018. С. 898-903
GOLD AND SILVER NANOPARTICLE-CATALYZED SYNTHESIS OF HETEROCYCLIC COMPOUNDS СтатьяKaur R., Bariwal J., Voskressensky L.G., Van Der Eycken E.V.Chemistry of Heterocyclic Compounds. Том 54. 2018. С. 241-248
INTERACTION OF CONDENSED TETRAHYDROPYRIDO[4,3-D]PYRIMIDIN-4-ONES WITH DEHYDROBENZENE – SYNTHESIS OF 6-VINYLPYRIMIDINONES FUSED WITH FIVE-MEMBERED HETEROCYCLE CONTAINING TWO OR THREE HETEROATOMS СтатьяVarlamov A.V., Guranova N.I., Borisova T.N., Sorokina E.A., Aksenov A.V., Voskressensky L.G.Chemistry of Heterocyclic Compounds. Том 54. 2018. С. 173-176
GOLD-CATALYZED POST-MCR TRANSFORMATIONS TOWARDS COMPLEX (POLY)HETEROCYCLES СтатьяSharma U.K., Tian G., Voskressensky L.G., Van Der Eycken E.V.Drug Discovery Today: Technologies. 2018.
UNEXPECTED CYCLIZATION OF 2-(2-AMINOPHENYL)INDOLES WITH NITROALKENES TO FURNISH INDOLO[3,2-: C] QUINOLINES СтатьяAksenov A.V., Aksenov D.A., Griaznov G.D., Aksenov N.A., Voskressensky L.G., Rubin M.Organic and Biomolecular Chemistry. Том 16. 2018. С. 4325-4332
DESIGN OF NEW ANTI-ALZHEIMER DRUGS: RING-EXPANSION SYNTHESIS AND SYNCHROTRON X-RAY DIFFRACTION STUDY OF DIMETHYL 4-ETHYL-11-FLUORO-1,4,5,6,7,8-HEXAHYDROAZONINO[5,6-B]INDOLE-2,3-DICARBOXYLATE СтатьяToze F.A.A., Listratova A.V., Voskressensky L.G., Chernikova N.Yu., Lobanov N.N., Bilyachenko A.N., Dorovatovskii P.V.Acta Crystallographica Section E: Crystallographic Communications. Том 74. 2018. С. 298-301
REACTION OF BENZYNE WITH 1,2,3,4-TETRAHYDROISOQUINOLINES AS AN ACCESS TO 1H-3-BENZAZEPINES СтатьяGuranova N.I., Varlamov A.V., Novikov R.A., Aksenov A.V., Borisova T.N., Sorokina E.A., Voskressensky L.G.Mendeleev Communications. Том 28. 2018. С. 22-24
SYNTHESIS AND CYTOTOXICITY OF DIBENZO[(Γ-ARYL)PYRIDINO]AZA-17-CROWN-5 ETHERS СтатьяAnh L.T., Phuong N.T.T., Hieu T.H., Soldatenkov A.T., Van B.T., Van T.T.T., Nhung D.T., Voskressensky L.G., Tung T.H., Khrustalev V.N.Macroheterocycles. Том 11. 2018. С. 197-202
СИЛИЛИРОВАНИЕ С ГЕНЕРАЦИЕЙ ФИКСИРОВАННОГО ЗАРЯДА ДЛЯ АНАЛИЗА СПИРТОВ МЕТОДОМ МАСС-СПЕКТРОМЕТРИИ МАЛДИ И ПАЛДИ СтатьяЖиляева Д.И., Воскресенский Л.Г., Половков Н.Ю., Борисов Р.С.Масс-спектрометрия. Том 15. 2018. С. 22-25
СОВРЕМЕННЫЕ ТЕНДЕНЦИИ ОРГАНИЧЕСКОЙ ХИМИИ В УНИВЕРСИТЕТАХ РОССИИ СтатьяКоновалов А.И., Антипин И.С., Бурилов В.А., Маджидов Т.И., Курбангалиева А.Р., Немтарев А.В., Соловьева С.Е., Стойков И.И., Мамедов В.А., Захарова Л.Я., Гаврилова Е.Л., Синяшин О.Г., Балова И.А., Васильев А.В., Зенкевич И.Г., Красавин М.Ю., Кузнецов М.А., Молчанов А.П., Новиков М.С., Николаев В.А. ...ЖУРНАЛ ОРГАНИЧЕСКОЙ ХИМИИ. Том 54. 2018. С. 161-360
EXPANDING THE REACTIVITY OF DONOR-ACCEPTOR CYCLOPROPANES: SYNTHESIS OF BENZANNULATED FIVE-MEMBERED HETEROCYCLES VIA INTRAMOLECULAR ATTACK OF A PENDANT NUCLEOPHILIC GROUP СтатьяIvanova O.A., Andronov V.A., Vasin V.S., Shumsky A.N., Rybakov V.B., Voskressensky L.G., Trushkov I.V.Organic Letters. Том 20. 2018. С. 7947-7952
DOMINO REACTIONS OF VINYL ETHYNYL KETONES WITH 1-ARYL-3,4-DIHYDROISOQUINOLINES — SEARCH FOR SELECTIVITY СтатьяMatveeva M., Golovanov A., Borisova T., Titov A., Varlamov A., Shaabani A., Obydennik A., Voskressensky L.Molecular Catalysis. Том 461. 2018. С. 67-72
SYNTHESIS OF 1-(PARA-METHOXYPHENYL)TETRAZOLYL-SUBSTITUTED 1,2,3,4-TETRAHYDROISOQUINOLINES AND THEIR TRANSFORMATIONS INVOLVING ACTIVATED ALKYNES СтатьяTitov A.A., Samavati R., Alexandrova E.V., Borisova T.N., Nguyen V.T., Le T.A., Varlamov A.V., Voskressensky L.G., Dang Thi T.A., Van Der Eycken E.V.Molecules. Том 23. 2018.
RECENT ADVANCES IN PHTHALAN AND COUMARAN CHEMISTRY СтатьяEfimov Ilya, Kulikova L., Van Der Eycken E.V., Voskressensky L.ChemistryOpen. Том 7. 2018. С. 914-929