Просмотр коллекции по группе - По автору Bakulev, V. A.

Перейти к: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
А Б В Г Д Е Ж З И Й К Л М Н О П Р С Т У Ф Х Ц Ч Ш Щ Ъ Ы Ь Э Ю Я
или введите несколько первых букв:  
Отображение результатов 1 до 20 из 32  дальше >
Дата публикацииНазваниеАвторы
2001Application of the Hurd-Mori reaction for the synthesis of chiral 1,2,3-thia(seleno)diazole derivatives from (+)-3-carene and α-pineneMorzherin, Yu. Yu.; Glukhareva, T. V.; Mokrushin, V. S.; Tkachev, A. V.; Bakulev, V. A.
2020A Base-Controlled Reaction of 2-Cyanoacetamidines (3,3-Diaminoacrylonitriles) with Sulfonyl Azides as a Route to Nonaromatic 4-Methylene-1,2,3-triazole-5-iminesSilaichev, P. S.; Beryozkina, T. V.; Novikov, M. S.; Dehaen, W.; Bakulev, V. A.
2023Cyanothioacetamides as a synthetic platform for the synthesis of aminopyrazole derivativesFilimonov, V. O.; Topchiy, A. I.; Ilkin, V. G.; Beryozkina, T. V.; Bakulev, V. A.
2024Development of A. Solani β-tubulin Models and Comparison of Docking Results for Benzo[d]azoles Derivatives as Potential Antifungal AgentsObydennov, K. L.; Kalinina, T. A.; Glukhareva, T. V.; Bakulev, V. A.
2023Differentiation between Isomeric 4,5-Functionalized 1,2,3-Thiadiazoles and 1,2,3-Triazoles by ESI-HRMS and IR Ion SpectroscopyMazur, D. M.; Piacentino, E. L.; Berden, G.; Oomens, J.; Ryzhov, V.; Bakulev, V. A.; Lebedev, A. T.
2020Facile one-pot synthesis of pharmacologically relevant 1,2,3-triazoles linked to equolJoy, M. N.; Beliaev, N. A.; Beryozkina, T. V.; Bakulev, V. A.
2019Is Nonaflate a Better Leaving Group Than Corresponding Triflate? A Case Study in the Palladium Catalyzed Cross-Coupling Reaction of 7-Substituted CoumarinsJoy, M. N.; Bakulev, V. A.
2019Is nonaflate a better leaving group than corresponding triflate? A case study in the palladium catalyzed cross-coupling reaction of 7-substituted coumarinsJoy, M. N.; Bakulev, V. A.
2013New opportunities for the synthesis of quinoxaline-substituted heterocyclic and aryl moietiesAzev, Y. A.; Kodess, M. I.; Ezhikova, M. A.; Gibor, A. M.; Baranov, V. I.; Ermakova, O. S.; Bakulev, V. A.
2018New Transformations of N-hetarylcyclopentano[d][1,2,3]triazoline Ring into 5-alkoxyvaleramidinesBelyaev, N. A.; Beryozkina, T. V.; Lubec, G.; Dehaen, W.; Bakulev, V. A.
2012Novel method for the synthesis of 4-(azol-5-yl)-1,2,3-triazolesBakulev, V. A.; Efimov, I. V.; Belyaev, N. A.; Rozin, Yu. A.; Volkova, N. N.; El'Tsov, O. S.
2013Novel method for the synthesis of 4-(azol-5-yl)isoxazolesBakulev, V. A.; Efimov, I. V.; Belyaev, N. A.; Zhidovinov, S. S.; Rozin, Y. A.; Volkova, N. N.; Khabarova, A. A.; Ele'tsov, O. S.
2013Reactions of 3-phenyl-1,2,4-triazine with some C-nucleophilesAzev, Y. A.; Ermakova, O. S.; Kodess, M. I.; Ezhikova, M. A.; Kovalev, I. S.; Bakulev, V. A.
2022Selective Synthesis of Azoloyl NH-1,2,3-Triazoles and Azolyl Diazoketones: Experimental and Computational InsightsShafran, Y. M.; Hussein, A. A.; Beliaev, N. A.; Shevyrin, V. A.; Shityakov, S.; Beryozkina, T. V.; Bakulev, V. A.
2020Suzuki-Miyaura coupling under microwave enhanced conditions: Synthesis of 2-(hetero)aryl benzimidazolesKaruvalam, R. P.; Haridas, K. R.; Sajith, A. M.; Pakkath, R.; Bhaskaran, S.; Padusha, M. S. A.; Bakulev, V. A.; Joy, M. N.
2008Synthesis and oxidative cyclization of 2-arylhydrazono-2-cyanoacetamidines to 5-amino-2-aryl-2H-[1,2,3]triazole-4-carbonitrileBel'Skaya, N. P.; Demina, M. A.; Sapognikova, S. G.; Fan, Z. -J.; Zhang, H. -K.; Dehaen, W.; Bakulev, V. A.
2019Synthesis and Pharmacological Study of Novel Benzotriazoles Containing AmidesMuthipeedika Nibin Joy; Bakulev, V. A.; Saveliev, D.
2010Synthesis and properties of hydrazones bearing amide, thioamide and amidine functionsBelskaya, N. P.; Dehaen, W.; Bakulev, V. A.
2019Synthesis and Reactivity of Azides Towards EnaminesDehaen, W.; Bakulev, V. A.; Beryozkina, T. V.; Saveliev, D. A.
2013Synthesis 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 interactionSadchikova, E. V.; Bakulev, V. A.; Subbotina, J. O.; Privalova, D. L.; Dehaen, W.; Van Hecke, K.; Robeyns, K.; Van Meervelt, L.; Mokrushin, V. S.