THE DEVELOPMENT OF METHODS FOR THE SYNTHESIS OF PYRROLO[2,1-A][2]BENZAZEPINES ArticleKhvostova P.E., Nevskaya A.A., Borisova T.N.Успехи синтеза и комплексообразования = Advances in synthesis and complexing. 2022. 187 с.
SWITCHABLE LIGHT VS. ACID-INDUCED TRANSFORMATIONS OF COMPLEX FRAMEWORK COMPOUNDS AT ROOM TEMPERATURE ArticleKobzev M.S., Titov A.A., Borisova T.N., Voskressensky L.G., Varlamov A.V., D'alterio M.C., Petrone A., Luque R., Talarico G.Green Chemistry. 2022.
HOMOBIVALENT LAMELLARIN-LIKE SCHIFF BASES: IN VITRO EVALUATION OF THEIR CANCER CELL CYTOTOXICITY AND MULTITARGETING ANTI-ALZHEIMER’S DISEASE POTENTIAL ArticleNevskaya A.A., Anikina L.V., Purgatorio R., Catto M., Nicolotti O., Pisani L., Borisova T.N., Miftyakhova A.R., Varlamov A.V., Nevskaya E.Yu., Borisov R.S., Voskressensky L.G., Altomare C.D., De Candia M.Molecules. Том 26. 2021.
SYNTHESIS AND CYTOTOXICITY OF NOVEL 1-ARYLINDOLIZINES AND 1-ARYLPYRROLO[2,1-A]ISOQUINOLINES ArticleNevskaya A.A., Miftyakhova A.R., Anikina L.V., Borisova T.N., Varlamov A.V., Voskressensky L.G.Tetrahedron Letters. 2021.
AWAY FROM FLATNESS: UNPRECEDENTED NITROGEN-BRIDGED CYCLOPENTA[ A]INDENE DERIVATIVES AS NOVEL ANTI-ALZHEIMER MULTITARGET AGENTS ArticleTitov A.A., Kobzev M.S., Catto M., Gambacorta N., Denora N., Pisani L., Nicolotti O., Borisova T.N., Varlamov A.V., Voskressensky L.G., Altomare C.D., De Candia M.ACS Chemical Neuroscience. Том 12. 2021. С. 340-353
SYNTHESIS OF 8-PHENYL SUBSTITUTED 3-BENZAZECINES WITH ALLENE MOIETY, THEIR THERMAL REARRANGEMENT AND EVALUATION AS ACETYLCHOLINESTERASE INHIBITORS ArticleKobzev M.S., Titov A.A., Alexandrova E.V., Purgatorio R., Catto M., Sorokina E.A., Borisova T.N., Varlamov A.V., Altomare C.D., Voskressensky L.G.MOLECULAR DIVERSITY. 2021.
TACTICS OF CHEMORADIOTHERAPY IN PATIENTS WITH LOCALLY ADVANCED SQUAMOUS CELL CARCINOMA OF THE PHARYNX WITH INDEX OF METASTATIC REGIONAL LYMPH NODES STAGE N3 ArticleАлиева С.Б., Задеренко И.А., Борисова Т.Н., Каледин Р.Р., Секретная А.О., Хромушина А.В.Опухоли головы и шеи. Том 11. 2021. С. 25-30
A THREE-COMPONENT SYNTHESIS OF 3-FUNCTIONALLY SUBSTITUTED 5,6-DIHYDROPYRROLO[2,1-A]ISOQUINOLINES ArticleMiftyakhova A.R., Borisova T.N., Titov A.A., Sidakov M.B., Novikov R.A., Efimov I.V., Varlamov A.V., Voskressensky L.G.Chemistry and Biodiversity. 2021.
СИНТЕЗ 4-ТЕТРАЗОЛИЛЗАМЕЩЁННЫХ ТИЕНОПИРИДИНОВ И АPОЦИНОВ ArticleСбеи Н., Титов А.А., Варламов А.В., Борисова Т.Н., Кобзев М.С., Нгуен Ван Т., Ле Туань А.Актуальные вопросы органической химии и биотехнологии. 2020. С. 249-250
FACILE SYNTHESIS OF PYRROLO[2,1-A]ISOQUINOLINES BY DOMINO REACTION OF 1-AROYL-3,4-DIHYDROISOQUINOLINES WITH CONJUGATED KETONES, NITROALKENES AND NITRILES ArticleAstakhov G.S., Shigaev R.R., Borisova T.N., Ershova A.A., Titov A.A., Varlamov A.V., Voskressensky L.G., Matveeva M.D.MOLECULAR DIVERSITY. 2020.
UNUSUAL TRANSFORMATIONS OF CYCLIC ALLENES WITH AN ENAMINE MOIETY INTO COMPLEX FRAMEWORKS ArticleTitov A.A., Kobzev M.S., Borisova T.N., Sorokina E.A., Varlamov A.V., Voskressensky L.G., Van Der Eycken E.Synlett. Том 31. 2020. С. 672-676
FACILE METHODS FOR THE SYNTHESIS OF 8-YLIDENE-1,2,3,8-TETRAHYDROBENZAZECINES ArticleTitov A.A., Kobzev M.S., Borisova T.N., Listratova A.V., Evenko T.V., Varlamov A.V., Voskressensky L.G.European Journal of Organic Chemistry. Том 2020. 2020. С. 3041-3049
FACILE SYNTHESIS AND BIOLOGICAL EVALUATION OF NEW THIENO[2,3-G]INDOLIZINE DERIVATIVES ArticleZinoveva A.D., Borisova T.N., Politova P.A., Titov A.A., Varlamov A.V., Voskressensky L.G., Nguyen V.T., Le T.A.ChemistrySelect. Том 5. 2020. С. 10821-10826
ДОМИНО-РЕАКЦИИ ГЕТЕРОЦИКЛОВ, СОДЕРЖАЩИХ ИМИНО-КЕТОННЫЙ ФРАГМЕНТ, С УЧАСТИЕМ ЭЛЕКТРОНОДЕФИЦИТНЫХ АЛКЕНОВ И АЛКИНОВ ArticleБорисова Т.Н., Матвеева М.Д., Невская А.А., Мифтяхова А.Р., Зиновьева А.Д., Варламов А.В., Воскресенский Л.Г.Актуальные вопросы органической химии и биотехнологии. 2020. С. 83-85
DOMINO-REACTIONS OF 1-AROYL-3,4-DIHYDROBENZO[H]ISOQUINOLINES WITH ACTIVATED ALKYNES AND ALKENES ArticleErshova A.A., Borisova T.N., Voskressensky L.G., Nguyen V.T., Le T.A.Advances in synthesis and complexing. 2019. 129 с.