Эта публикация цитируется в 15 научных статьях (всего в 15 статьях)
Communications
Sodium acetate catalyzed multicomponent approach to medicinally privileged 2-amino-4H-chromene scaffold from salicylaldehydes, malononitrile and cyanoacetates
Аннотация:
Sodium acetate-catalyzed multicomponent assembling of salicylaldehydes, malononitrile and cyanoacetates in water–alcohol mixture (1: 1) at ambient temperature affords alkyl (2-amino-3-cyano-4H-chromen-4-yl)cyanoacetates in 88–95% yields.
Образец цитирования:
M. N. Elinson, F. V. Ryzhkov, R. F. Nasybullin, T. A. Zaimovskaya, M. P. Egorov, “Sodium acetate catalyzed multicomponent approach to medicinally privileged 2-amino-4H-chromene scaffold from salicylaldehydes, malononitrile and cyanoacetates”, Mendeleev Commun., 24:3 (2014), 170–172
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc2513
https://www.mathnet.ru/rus/mendc/v24/i3/p170
Эта публикация цитируется в следующих 15 статьяx:
Rahul A Nagarkar, Sudhir E Dapurkar, “Disodium Anacardate: A Bio-based Catalyst for Room Temperature Synthesis of New, Fluorescent 1, 4-Benzoxazinone and Benzophenoxazinone Derivatives”, J Chem Sci, 134:3 (2022)
Majid Heravi, Vahideh Zadsirjan, Recent Advances in Applications of Name Reactions in Multicomponent Reactions, 2020, 269
M. N. Elinson, A. N. Vereshchagin, Y. E. Anisina, A. S. Goloveshkin, I. E. Ushakov, M. P. Egorov, “Multicomponent transformation of salicylaldehydes, 2-aminoprop-1-ene-1,1,3-tricarbonitrile, and pyrazolin-5-ones into substituted 2,4-diamino-5-(5-hydroxy-3-methyl-1H-pyrazol-4-yl)-5H-chromeno[2,3-b]pyridine-3-carbonitriles”, Russ Chem Bull, 67:9 (2018), 1695
Michail N. Elinson, Anatoly N. Vereshchagin, Alexander D. Korshunov, Mikhail P. Egorov, “A fast and efficient 'on-solvent' cascade assembling of salicylaldehydes and dimethylbarbituric acid into 5-(1,3-dimethyl-2,4-dioxo-1,3,4,5-tetrahydro-2H-chromeno[2,3-d]pyrimidin-5-yl)-1,3-dimethylpyrimidine-2,4,6(1H,3H,5H)-triones”, Heterocyclic Communications, 24:2 (2018), 79
M. N. Elinson, A. N. Vereshchagin, Yu. E. Anisina, A. S. Goloveshkin, I. E. Ushakov, M. P. Egorov, “PASE facile and efficient multicomponent approach to the new type of 5-C-substituted 2,4-diamino-5H-chromeno[2,3-b]pyridine scaffold”, Mendeleev Commun., 28:4 (2018), 372–374
Majid M. Heravi, Vahideh Zadsirjan, Malihe Mollaiye, Masumeh Heydari, Afsaneh Taheri Kal Koshvandi, “Salicylaldehydes as privileged synthons in multicomponent reactions”, Усп. хим., 87:6 (2018), 553–585; Majid M. Heravi, Vahideh Zadsirjan, Malihe Mollaiye, Masumeh Heydari, Afsaneh Taheri Kal Koshvandi, “Salicylaldehydes as privileged synthons in multicomponent reactions”, Russian Chem. Reviews, 87:6 (2018), 553–585
M. N. Elinson, F. V. Ryzhkov, A. N. Vereshchagin, A. D. Korshunov, R. A. Novikov, M. P. Egorov, “'On-solvent' new domino reaction of salicylaldehyde, malononitrile and 4-hydroxy-6-methylpyridin-2(1H)-one: fast and efficient approach to medicinally relevant 4-pyridinyl-2-amino-4H-chromene scaffold”, Mendeleev Commun., 27:6 (2017), 559–561
Michail N. Elinson, Fedor V. Ryzhkov, Victor A. Korolev, Mikhail P. Egorov, “Pot, atom and step-economic (PASE) synthesis of medicinally relevant spiro[oxindole-3,4′-pyrano[4,3-b]pyran] scaffold”, Heterocyclic Communications, 22:1 (2016), 11
Michail N. Elinson, Fedor V. Ryzhkov, Ruslan F. Nasybullin, Anatoly N. Vereshchagin, Mikhail P. Egorov, “Fast Efficient and General PASE Approach to Medicinally Relevant 4H,5H‐Pyrano‐[4,3‐b]pyran‐5‐one and 4,6‐Dihydro‐5H‐pyrano‐[3,2‐c]pyridine‐5‐one Scaffolds”, Helvetica Chimica Acta, 99:9 (2016), 724
M. N. Elinson, F. V. Ryzhkov, A. N. Vereshchagin, T. A. Zaimovskaya, V. A. Korolev, M. P. Egorov, “Multicomponent assembling of isatins, malononitrile and 4-hydroxy-6-methylpyridin-2(1H)-ones: one-pot efficient approach to privileged spiro[indoline-3,4'-pyrano[3,2-c]pyridine]-2,5'(6'H)-dione scaffold”, Mendeleev Commun., 26:5 (2016), 399–401
Anatoly N. Vereshchagin, Michail N. Elinson, Ruslan F. Nasybullin, Fedor V. Ryzhkov, Sergey I. Bobrovsky, Ivan S. Bushmarinov, Mikhail P. Egorov, “One‐Pot 'On‐solvent' Multicomponent Protocol for the Synthesis of Medicinally Relevant 4H‐Pyrano[3,2‐c]quinoline Scaffold”, Helvetica Chimica Acta, 98:8 (2015), 1104
Yufeng Ren, Wei Zhang, Jun Lu, Kai Gao, Xiali Liao, Xiaozhen Chen, “One-pot synthesis of tetrahydro-4H-chromenes by supramolecular catalysis in water”, RSC Adv., 5:97 (2015), 79405
Anatoly N. Vereshchagin, Michail N. Elinson, Fedor V. Ryzhkov, Ruslan F. Nasybullin, Sergey I. Bobrovsky, Alexander S. Goloveshkin, Mikhail P. Egorov, “Multicomponent assembling of salicylaldehydes, malononitrile, and 4-hydroxy-6-methyl-2H-pyran-2-one: A fast and efficient approach to medicinally relevant 2-amino-4H-chromene scaffold”, Comptes Rendus. Chimie, 18:12 (2015), 1344
Michail N. Elinson, Fedor V. Ryzhkov, Anatoly N. Vereshchagin, Sergey V. Gorbunov, Mikhail P. Egorov, “Multicomponent assembling of salicylaldehydes, malononitrile and cyanoacetamides: A simple and efficient approach to medicinally relevant 2-amino-4H-chromene scaffold”, Comptes Rendus. Chimie, 18:5 (2015), 540
Michail N. Elinson, Fedor V. Ryzhkov, Ruslan F. Nasybullin, Tatiana A. Zaimovskaya, Mikhail P. Egorov, “ChemInform Abstract: Sodium Acetate Catalyzed Multicomponent Approach to Medicinally Privileged 2‐Amino‐4H‐chromene Scaffold from Salicylaldehydes, Malononitrile and Cyanoacetates.”, ChemInform, 45:42 (2014)