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.
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
ТАКТИКА ХИМИОЛУЧЕВОЙ ТЕРАПИИ БОЛЬНЫХ МЕСТНО-РАСПРОСТРАНЕННЫМ ПЛОСКОКЛЕТОЧНЫМ РАКОМ ГЛОТКИ СТАДИИ 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
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.
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.
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
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.
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 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
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
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
DOMINO REACTIONS OF 4-AROYL-6,7-DIHYDROTHIENOPYRIDINES WITH ELECTRON DEFICIENT ALKYNES AND ALKENES ArticleZinoveva A.D., Borisova T.N., Dyachenko S.V., Nguyen V.T., Le T.A.Advances in synthesis and complexing. 2019. 288 с.
DOMINO REACTIONS OF 1-ARYL-3,4-DIHYDROISOQUINOLINES WITH CROSS-CONJUGATED KETONES - SEARCH FOR SELECTIVITY ArticleObydennik A.Y., Matveeva M.D., Borisova T.N.Advances in synthesis and complexing. 2019. 209 с.
3-BENZAZECINE-BASED CYCLIC ALLENE DERIVATIVES AS HIGHLY POTENT P-GLYCOPROTEIN INHIBITORS OVERCOMING DOXORUBICIN MULTIDRUG RESISTANCE ArticleTitov A.A., Niso M., Candia M., Kobzev M.S., Varlamov A.V., Borisova T.N., Voskressensky L.G., Colabufo N.A., Cellamare S., Pisani L., Altomare C.D.Future medicinal chemistry. Том 11. 2019. С. 2095-2106