EVALUATION OF WATER-SOLUBLE MANNICH BASE PRODRUGS OF 2,3,4,5-TETRAHYDROAZEPINO[4,3-B]INDOL-1(6H)-ONE AS MULTITARGET-DIRECTED AGENTS FOR ALZHEIMER'S DISEASE ArticlePurgatorio R., Catto M., Rullo M., Pisani L., Denora N., Carrieri A., Nevskaya A.A., Voskressensky L.G., Altomare C.D., De Candia M.ChemMedChem. Том 16. 2021. С. 589-598
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.
PROFESSOR, DOCTOR OF SCIENCES IN CHEMISTRY ALEXANDER VIKTOROVICH AKSENOV TO THE 55TH BIRTHDAY ArticleVoskressensky L.G.Chemistry of Heterocyclic Compounds. Том 57. 2021. С. 613-614
SUPPORTED PHOSPHINE FREE BIS-NHC PALLADIUM PINCER COMPLEX: AN EFFICIENT REUSABLE NANOCATALYST FOR SUZUKI-MIYAURA COUPLING REACTION ArticleRajabi F., Burange A.S., Voskressensky L.G., Luque R.Molecular Catalysis. Том 515. 2021.
RECENT ADVANCES FOR THE SYNTHESIS OF N-UNSUBSTITUTED PYRROLES ArticleEfimov I.V., Kulikova L.N., Miftyakhova A.R., Matveeva M.D., Voskressensky L.G.ChemistrySelect. Том 6. 2021. С. 13740-13772
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.
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
INSIGHTS INTO THE BINDING INTERACTION MECHANISM OF 12,12-DIHYDROCHROMENO[2,3-C]ISOQUINOLIN-5-AMINE IN BOVINE SERUM ALBUMIN AND PROSTAGLANDIN H2 SYNTHASE-1: A BIOPHYSICAL APPROACH ArticleKarthikeyan S., Yue X., Festa A.A., Voskressensky L.G.Journal of Molecular Structure. Том 1245. 2021.
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
RECENT DEVELOPMENTS IN TRANSITION-METAL CATALYZED DIRECT C-H ALKENYLATION, ALKYLATION, AND ALKYNYLATION OF AZOLES ArticleChen S., Ranjan P., Voskressensky L.G., Sharma U.K., Van Der Eycken E.V.Molecules. Том 25. 2020.
A FACILE ONE-POT SYNTHESIS OF 1,2,3,4-TETRAHYDROISOQUINOLINE-1-CARBONITRILES VIA THE ELECTROGENERATED CYANIDE ANIONS FROM ACETONITRILE ArticleSbei N., Titov A.A., Markova E.B., Elinson M.N., Voskressensky L.G.ChemistrySelect. Том 5. 2020. С. 4493-4495
GREEN SYNTHESIS OF POLYSUBSTITUTED PYRROLES THROUGH A DOMINO SEQUENCE OF AZA-CLAISEN REARRANGEMENT/NUCLEOPHILIC ADDITION/OXIDATION/ACYLATION ArticleGolubenkova A.S., Golantsov N.E., Varlamov A.V., Voskressensky L.G.Актуальные вопросы органической химии и биотехнологии. 2020. С. 44-46
MICROWAVE-ASSISTED SEQUENTIAL THREE-COMPONENT SYNTHESIS OF PYRROLYL-SUBSTITUTED CHROMENO[2,3-C]ISOQUINOLIN-5-AMINES ArticleYue X., Storozhenko O.A., Festa A.A., Sorokina E.A., Varlamov A.V., Voskressensky L.G.Chemistry of Heterocyclic Compounds. Том 56. 2020. С. 495-498
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
REDUCTIVE DOMINO REACTION TO ACCESS CHROMENO[2,3-C]ISOQUINOLINE-5-AMINES WITH ANTIPROLIFERATIVE ACTIVITIES AGAINST HUMAN TUMOR CELLS ArticleYue X., Festa A.A., Storozhenko O.A., Varlamov A.V., Subramani K., Boccarelli A., Purgatorio R., Altomare C.D., Voskressensky L.G.Bioorganic Chemistry. Том 104. 2020.