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ISSN:
2310-757X
Электронный научный архив УрФУ
Browsing by Author Bakulev, V. A.
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Showing results 1 to 20 of 32
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Issue Date
Title
Author(s)
2001
Application of the Hurd-Mori reaction for the synthesis of chiral 1,2,3-thia(seleno)diazole derivatives from (+)-3-carene and α-pinene
Morzherin, Yu. Yu.
;
Glukhareva, T. V.
;
Mokrushin, V. S.
;
Tkachev, A. V.
;
Bakulev, V. A.
2020
A Base-Controlled Reaction of 2-Cyanoacetamidines (3,3-Diaminoacrylonitriles) with Sulfonyl Azides as a Route to Nonaromatic 4-Methylene-1,2,3-triazole-5-imines
Silaichev, P. S.
;
Beryozkina, T. V.
;
Novikov, M. S.
;
Dehaen, W.
;
Bakulev, V. A.
2023
Cyanothioacetamides as a synthetic platform for the synthesis of aminopyrazole derivatives
Filimonov, V. O.
;
Topchiy, A. I.
;
Ilkin, V. G.
;
Beryozkina, T. V.
;
Bakulev, V. A.
2024
Development of A. Solani β-tubulin Models and Comparison of Docking Results for Benzo[d]azoles Derivatives as Potential Antifungal Agents
Obydennov, K. L.
;
Kalinina, T. A.
;
Glukhareva, T. V.
;
Bakulev, V. A.
2023
Differentiation between Isomeric 4,5-Functionalized 1,2,3-Thiadiazoles and 1,2,3-Triazoles by ESI-HRMS and IR Ion Spectroscopy
Mazur, D. M.
;
Piacentino, E. L.
;
Berden, G.
;
Oomens, J.
;
Ryzhov, V.
;
Bakulev, V. A.
;
Lebedev, A. T.
2020
Facile one-pot synthesis of pharmacologically relevant 1,2,3-triazoles linked to equol
Joy, M. N.
;
Beliaev, N. A.
;
Beryozkina, T. V.
;
Bakulev, V. A.
2019
Is Nonaflate a Better Leaving Group Than Corresponding Triflate? A Case Study in the Palladium Catalyzed Cross-Coupling Reaction of 7-Substituted Coumarins
Joy, M. N.
;
Bakulev, V. A.
2019
Is nonaflate a better leaving group than corresponding triflate? A case study in the palladium catalyzed cross-coupling reaction of 7-substituted coumarins
Joy, M. N.
;
Bakulev, V. A.
2013
New opportunities for the synthesis of quinoxaline-substituted heterocyclic and aryl moieties
Azev, Y. A.
;
Kodess, M. I.
;
Ezhikova, M. A.
;
Gibor, A. M.
;
Baranov, V. I.
;
Ermakova, O. S.
;
Bakulev, V. A.
2018
New Transformations of N-hetarylcyclopentano[d][1,2,3]triazoline Ring into 5-alkoxyvaleramidines
Belyaev, N. A.
;
Beryozkina, T. V.
;
Lubec, G.
;
Dehaen, W.
;
Bakulev, V. A.
2012
Novel method for the synthesis of 4-(azol-5-yl)-1,2,3-triazoles
Bakulev, V. A.
;
Efimov, I. V.
;
Belyaev, N. A.
;
Rozin, Yu. A.
;
Volkova, N. N.
;
El'Tsov, O. S.
2013
Novel method for the synthesis of 4-(azol-5-yl)isoxazoles
Bakulev, V. A.
;
Efimov, I. V.
;
Belyaev, N. A.
;
Zhidovinov, S. S.
;
Rozin, Y. A.
;
Volkova, N. N.
;
Khabarova, A. A.
;
Ele'tsov, O. S.
2013
Reactions of 3-phenyl-1,2,4-triazine with some C-nucleophiles
Azev, Y. A.
;
Ermakova, O. S.
;
Kodess, M. I.
;
Ezhikova, M. A.
;
Kovalev, I. S.
;
Bakulev, V. A.
2022
Selective Synthesis of Azoloyl NH-1,2,3-Triazoles and Azolyl Diazoketones: Experimental and Computational Insights
Shafran, Y. M.
;
Hussein, A. A.
;
Beliaev, N. A.
;
Shevyrin, V. A.
;
Shityakov, S.
;
Beryozkina, T. V.
;
Bakulev, V. A.
2020
Suzuki-Miyaura coupling under microwave enhanced conditions: Synthesis of 2-(hetero)aryl benzimidazoles
Karuvalam, R. P.
;
Haridas, K. R.
;
Sajith, A. M.
;
Pakkath, R.
;
Bhaskaran, S.
;
Padusha, M. S. A.
;
Bakulev, V. A.
;
Joy, M. N.
2008
Synthesis and oxidative cyclization of 2-arylhydrazono-2-cyanoacetamidines to 5-amino-2-aryl-2H-[1,2,3]triazole-4-carbonitrile
Bel'Skaya, N. P.
;
Demina, M. A.
;
Sapognikova, S. G.
;
Fan, Z. -J.
;
Zhang, H. -K.
;
Dehaen, W.
;
Bakulev, V. A.
2019
Synthesis and Pharmacological Study of Novel Benzotriazoles Containing Amides
Muthipeedika Nibin Joy
;
Bakulev, V. A.
;
Saveliev, D.
2010
Synthesis and properties of hydrazones bearing amide, thioamide and amidine functions
Belskaya, N. P.
;
Dehaen, W.
;
Bakulev, V. A.
2019
Synthesis and Reactivity of Azides Towards Enamines
Dehaen, W.
;
Bakulev, V. A.
;
Beryozkina, T. V.
;
Saveliev, D. A.
2013
Synthesis and structure of new imidazo- and pyrazolo[5,1-d][1,2,3,5] thiatriazines based on the reaction of diazoazoles with acyl isothiocyanates controlled by Sa⋯O interaction
Sadchikova, E. V.
;
Bakulev, V. A.
;
Subbotina, J. O.
;
Privalova, D. L.
;
Dehaen, W.
;
Van Hecke, K.
;
Robeyns, K.
;
Van Meervelt, L.
;
Mokrushin, V. S.