MODERN TRENDS OF ORGANIC CHEMISTRY IN RUSSIAN UNIVERSITIES СтатьяKonovalov A.I., Antipin I.S., Burilov V.A., Madzhidov T.I., Kurbangalieva A.R., Nemtarev A.V., Solovieva S.E., Stoikov I.I., Mamedov V.A., Zakharova L.Y., Gavrilova E.L., Sinyashin O.G., Balova I.A., Vasilyev A.V., Zenkevich I.G., Krasavin M.Y., Kuznetsov M.A., Molchanov A.P., Novikov M.S., Nikolaev V.A. ...Russian Journal of Organic Chemistry. Том 54. 2018. С. 157-371
SYNTHESIS OF SYMMETRICAL CHROMENO[2,3-B]CHROMENES ON THE BASIS OF О-QUINONE METHIDES AND 1,1-BIS(MORPHOLINO)ETHENE СтатьяOsyanin V.A., Osipov D.V., Demidov M.R., Krasnikov P.E., Klimochkin Y.N.Chemistry of Heterocyclic Compounds. Том 53. 2017. С. 1310-1314
REACTIONS OF 1-[(DIMETHYLAMINO)METHYL]NAPHTHALEN-2-OLS WITH CYCLIC PUSH-PULL NITROENAMINES СтатьяLukashenko A.V., Osipov D.V., Osyanin V.A., Klimochkin Y.N.Chemistry of Heterocyclic Compounds. Том 53. 2017. С. 1369-1372
ORTHO-QUINONE METHIDES AS KEY INTERMEDIATES IN CASCADE HETEROCYCLIZATIONS СтатьяOsipov D.V., Osyanin V.A., Klimochkin Y.N.Russian Chemical Reviews. Том 86. 2017. С. 625-687
REACTION OF PUSH-PULL ENAMINOKETONES AND IN SITU GENERATED ORTHO-QUINONE METHIDES: SYNTHESIS OF 3-ACYL-4H-CHROMENES AND 2-ACYL-1H-BENZO[F]CHROMENES AS PRECURSORS FOR HYDROXYBENZYLATED HETEROCYCLES СтатьяLukashenko A.V., Osyanin V.A., Osipov D.V., Klimochkin Y.N.Journal of Organic Chemistry. Том 82. 2017. С. 1517-1528
OXIDATIVE REARRANGEMENT OF 4H-CHROMENES TO 2-AROYLBENZOFURANS IN THE PRESENCE OF SELENIUM DIOXIDE СтатьяDemidov M.R., Lapshina M.Y., Osipov D.V., Osyanin V.A., Klimochkin Y.N.Chemistry of Heterocyclic Compounds. Том 53. 2017. С. 1053-1056
REACTIONS OF O-QUINONE METHIDES WITH HALOGENATED 1H-AZOLES: ACCESS TO BENZO[E]AZOLO[1,3]OXAZINES СтатьяOsipov D.V., Osyanin V.A., Voskressensky L.G., Klimochkin Y.N.Synthesis. Том 49. 2017. С. 2286-2296
REACTION OF TRIFLUOROACETYLCHROMENES WITH 6-AMINOURACILS. SYNTHESIS OF PYRIDO[2,3-D]PYRIMIDINES СтатьяPopova Y.V., Osipov D.V., Osyanin V.A., Klimochkin Y.N.Russian Journal of Organic Chemistry. Том 53. 2017. С. 599-603