A THREE-COMPONENT SYNTHESIS OF 3-FUNCTIONALLY SUBSTITUTED 5,6-DIHYDROPYRROLO[2,1-A]ISOQUINOLINES Article Miftyakhova 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. Wiley-VCH Verlag. 2021.
SYNTHESIS OF 8-PHENYL SUBSTITUTED 3-BENZAZECINES WITH ALLENE MOIETY, THEIR THERMAL REARRANGEMENT AND EVALUATION AS ACETYLCHOLINESTERASE INHIBITORS Article Kobzev 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. SPRINGER. 2021.
ДОМИНО-РЕАКЦИИ ГЕТЕРОЦИКЛОВ, СОДЕРЖАЩИХ ИМИНО-КЕТОННЫЙ ФРАГМЕНТ, С УЧАСТИЕМ ЭЛЕКТРОНОДЕФИЦИТНЫХ АЛКЕНОВ И АЛКИНОВ Article Борисова 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. Общество с ограниченной ответственностью "ИЗДАТЕЛЬСТВО АМБ". 2020. P. 83-85
FACILE METHODS FOR THE SYNTHESIS OF 8-YLIDENE-1,2,3,8-TETRAHYDROBENZAZECINES Article Titov 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. Vol. 2020. 2020. P. 3041-3049
FACILE SYNTHESIS OF PYRROLO[2,1-A]ISOQUINOLINES BY DOMINO REACTION OF 1-AROYL-3,4-DIHYDROISOQUINOLINES WITH CONJUGATED KETONES, NITROALKENES AND NITRILES Article Astakhov 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. SPRINGER. 2020.
FACILE SYNTHESIS AND BIOLOGICAL EVALUATION OF NEW THIENO[2,3-G]INDOLIZINE DERIVATIVES Article Zinoveva A.D., Borisova T.N., Politova P.A., Titov A.A., Varlamov A.V., Voskressensky L.G., Nguyen V.T., Le T.A. ChemistrySelect. Wiley-Blackwell. Vol. 5. 2020. P. 10821-10826
СИНТЕЗ 4-ТЕТРАЗОЛИЛЗАМЕЩЁННЫХ ТИЕНОПИРИДИНОВ И АPОЦИНОВ Article Сбеи 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. Общество с ограниченной ответственностью "ИЗДАТЕЛЬСТВО АМБ". 2020. P. 249-250
UNUSUAL TRANSFORMATIONS OF CYCLIC ALLENES WITH AN ENAMINE MOIETY INTO COMPLEX FRAMEWORKS Article Titov A.A., Kobzev M.S., Borisova T.N., Sorokina E.A., Varlamov A.V., Voskressensky L.G., Van Der Eycken E. Synlett. Vol. 31. 2020. P. 672-676
DOMINO REACTIONS OF 1-ARYL-3,4-DIHYDROISOQUINOLINES WITH CROSS-CONJUGATED KETONES - SEARCH FOR SELECTIVITY Article Obydennik A.Y., Matveeva M.D., Borisova T.N. Advances in synthesis and complexing. РУДН. 2019. 209 p.
1-AROYLISOQUINOLINE AND 2-BENZOYLPYRIDINE IN REACTIONS WITH ACROLEIN Article Nevskaya A.A., Miftyahova A.R., Borisova T.N., Voskressensky L.G., Varlamov A.V. Advances in synthesis and complexing. РУДН. 2019. 75 p.
SYNTHESIS OF 2-SUBSTITUTED PYRIDO[2,3-B]INDOLIZINE-10-CARBONITRILES - PROMISING COMPOUNDS WITH FLUORESCENT PROPERTIES Article Sokolova E.A., Festa A.A., Borisova T.N., Voskressensky L.G. Advances in synthesis and complexing. РУДН. 2019. 248 p.
3-BENZAZECINE-BASED CYCLIC ALLENE DERIVATIVES AS HIGHLY POTENT P-GLYCOPROTEIN INHIBITORS OVERCOMING DOXORUBICIN MULTIDRUG RESISTANCE Article Titov 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. NLM (Medline). Vol. 11. 2019. P. 2095-2106
DOMINO REACTIONS OF 4-AROYL-6,7-DIHYDROTHIENOPYRIDINES WITH ELECTRON DEFICIENT ALKYNES AND ALKENES Article Zinoveva A.D., Borisova T.N., Dyachenko S.V., Nguyen V.T., Le T.A. Advances in synthesis and complexing. РУДН. 2019. 288 p.
DOMINO-REACTIONS OF 1-AROYL-3,4-DIHYDROBENZO[H]ISOQUINOLINES WITH ACTIVATED ALKYNES AND ALKENES Article Ershova A.A., Borisova T.N., Voskressensky L.G., Nguyen V.T., Le T.A. Advances in synthesis and complexing. РУДН. 2019. 129 p.
NEW APPROACHES TO THE SYNTHESIS OF BENZO[H]PYRROLOISOQUINOLINE DERIVATIVES Article Ershova A.A., Zinoveva A.D., Borisova T.N., Titov A.A., Varlamov A.V., Voskressensky L.G., Tuyen Nguyen V., Anh Le T. Tetrahedron Letters. Elsevier Ltd. Vol. 60. 2019.