Maxim D. Gotsko

From 4,5,6,7-tetrahydroindoles to 3- or 5-(4,5,6,7-tetrahydroindol-2-yl)isoxazoles in two steps: a regioselective switch between 3- and 5-isomers

Lyubov N. Sobenina, Denis N. Tomilin, Maxim D. Gotsko et al. · Tetrahedron · 2014 · 26 citations

Engineering, Natural Sciences, Diversity-oriented Synthesis +7

Synthesis and Optical Properties of <i>meso</i>‐CF₃‐BODIPY with Acylethynyl Substituents in the 3‐Position of the Indacene Core

Denis N. Tomilin, Konstantin B. Petrushenko, Lyubov N. Sobenina et al. · Asian Journal of Organic Chemistry · 2016 · 21 citations

Materials Science, Organic Material Chemistry, Chemical Engineering +14

Catalyst-Free Annulation of Acylethynylpyrroles with 1-Pyrrolines: A Straightforward Access to Tetrahydrodipyrrolo[1,2-<i>a</i>:1′,2′-<i>c</i>]imidazoles

Ludmila A. Oparina, Kseniya V. Belyaeva, Nikita A. Kolyvanov et al. · The Journal of Organic Chemistry · 2022 · 19 citations

Topochemical mechanoactivated phosphonylethynylation of pyrroles with chloroethynylphosphonates on solid Al2O3 or K2CO3 media

Maxim D. Gotsko, Lyubov N. Sobenina, Denis N. Tomilin et al. · Tetrahedron Letters · 2015 · 16 citations

Solid Al2o3, Inorganic Chemistry, Materials Science +4

N-Vinyl-2-(trifluoroacetylethynyl)pyrroles and E-2-(1-bromo-2-trifluoroacetylethenyl)pyrroles: Cross-coupling vs. addition during C H-functionalization of pyrroles with bromotrifluoroacetylacetylene in solid Al2O3 medium. H-bonding control

Denis N. Tomilin, Maxim D. Gotsko, Lyubov N. Sobenina et al. · Journal of Fluorine Chemistry · 2016 · 15 citations

Chemical Engineering, Cross-coupling Reaction, Engineering +8