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Acylacetylenes in multiple functionalization of hydroxyquinolines and quinolones
Belyaeva K.V.
with acylacetylenes (20 mol% KOH, 5 equiv. H2O, MeCN, 55–60 °C), which, according to the previous finding, might
Azidothymidine "clicked" into 1,2,3-Triazoles: First Report on Carbonic Anhydrase-Telomerase Dual-Hybrid Inhibitors
Berrino E., Angeli A., Zhdanov D.D., Kiryukhina A.P., Milaneschi A., Bozdag M., Carradori S., Selleri S., Bartolucci G., Peat T.S., Ferraroni M., Supuran C.T., Carta F., De Luca A.
instead. In this context, we exploited the validated antitumor targets carbonic anhydrases (CAs; EC 4.2.1.1
(3aS,4R,5R,6S,7aR)-4,5-Di­bromo-2-[4-(tri­fluoro­meth­yl)phen­yl]-2,3,3a,4,5,6,7,7a-octa­hydro-3a,6-ep­oxy-1H-isoindol-1-one: Crystal structure and Hirshfeld surface analysis
Mertsalov D.F., Alekseeva K.A., Daria M.S., Cheshigin M.E., Celikesir S.T., Akkurt M., Grigoriev M.S., Mlowe S.
The asymmetric unit of the title compound, C15H12Br2F3NO2, consists of two crystallographically
Crystal structure and Hirshfeld surface analysis of 4,5-di­bromo-2-(4-meth­oxy­phen­yl)-2,3,4,4a,5,6,7,7a-octa­hydro-1H-4,6-ep­oxy-1H-cyclo­penta­[c]pyridin-1-one
Mertsalov D.F., Surina N.S., Sorokina E.A., Celikesir S.T., Akkurt M., Grigoriev M.S., Mlowe S.
The mol­ecule of the title compound, C15H15Br2NO3, comprises a fused tricyclic system consisting
Crystal structures and Hirshfeld surface analyses of (E)-1-[1-(4-tert-butyl­phen­yl)-2,2-di­chloro­ethen­yl]-2-phenyl­diazene, (E)-1-[1-(4-tert-butyl­phen­yl)-2,2-di­chloro­ethen­yl]-2-(4-methyl­phen­yl)diazene, (E)-1-[1-(4-tert-butyl­phen­yl)-2,2-di­chloro­ethen­yl]-2-(4-meth­oxy­phen­yl)diazene and (E)-1-[1-(4-tert-butyl­phen­yl)-2,2-di­chloro­ethen­yl]-2-(3-methyl­phen­yl)diazene
Maharramov A., Shikhaliyev N.Q., Qajar A., Atakishiyeva G.T., Niyazova A., Khrustalev V.N., Akkurt M., Yildirim S.Ö., Bhattarai A.
in the monoclinic space group C2/c with Z = 8, and (E)-1-[1-(4-tert-butyl­phen­yl)-2,2-di­chloro­ethen­yl]-2-(4-meth­oxy­phen­yl
(1 R,3 S)-3-(1 H -Benzo[ d ]imidazol-2-yl)-1,2,2-tri­methyl­cyclo­pentane-1-carb­oxy­lic acid as a new anti-diabetic active pharmaceutical ingredient
Kovalenko, S. M., Konovalova, I. S., Merzlikin, S. I., Chuev, V. P., Kravchenko, D. V.
, was prepared from (1R,3S)-camphoric acid and o-phenyl­enedi­amine. It crystallized from an ethanol solution
(1 R,3 S)-3-(1 H -Benzo[ d ]imidazol-2-yl)-1,2,2-tri­methyl­cyclo­pentane-1-carb­oxy­lic acid as a new anti-diabetic active pharmaceutical ingredient
Kovalenko, S. M., Konovalova, I. S., Merzlikin, S. I., Chuev, V. P., Kravchenko, D. V.
, was prepared from (1R,3S) - camphoric acid and o-phenylenediamine
Reaction of Substituted Chalcone with Guanidine in the Presence of Hydrogen Peroxide
Mamedov I.G., Khrustalev V.N.
Abstract: A new compound, 2-amino-5-(4-bromophenyl)-5-{5-bromo-2-[(prop-2-en-1-yl)oxy]benzyl}-3
Keto-oxy tautomerism
Fain V.Ya., Zaitsev B.E., Ryabov M.A.
Keto-oxy tautomerism
Hemorheological parameters and their correlations in OXYS rats: A new model of hyperviscosity syndrome
Maslov, Mikhail Y., Smolyakova, Vera I., Aliev, Oleg I., Kolosova, Natalia G., Plotnikov, Mark B., Chernysheva, Galina A.
rats at low (3–10 s−1) and high (45–300 s−1) shear rates were 14–20% and 7–10% higher than in Wistar

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