Эта публикация цитируется в 18 научных статьях (всего в 18 статьях)
Communications
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
Аннотация:
The new one-pot multicomponent assembling of isatins, malononitrile and 4 hydroxy-6-methylpyridin-2(1H)-ones into previously unknown 2’-amino-7’-methyl-2,5’-dioxo-5’,6’-dihydrospiro[indoline-3,4’-pyrano[3,2-c]pyridine]-3’-carbonitriles in 80–98% yields has been accomplished by their reflux in ethanol in the presence of sodium acetate.
Образец цитирования:
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
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc2226
https://www.mathnet.ru/rus/mendc/v26/i5/p399
Эта публикация цитируется в следующих 18 статьяx:
Fatemeh Asilpour, Dariush Saberi, Alireza Hasaninejad, “Synthesis of novel chromeno[1,6]naphthyridine derivatives in PEG-400 via catalyst-free, one-pot, and multicomponent reactions”, New J. Chem., 48:1 (2024), 237
Michail N. Elinson, Anatoly N. Vereshchagin, Yuliya E. Ryzhkova, Kirill A. Karpenko, Varvara M. Kalashnikova, “Cascade assembling of aldehydes and two molecules of dimedone into 4H-spiro[1-benzofuran-2,1'-cyclohexane]-2',4,6'-triones under column chromatography-free protocol at room temperature”, Chem Heterocycl Comp, 60:5-6 (2024), 239
Dipti B. Upadhyay, Ruturajsinh M. Vala, Subham G. Patel, Paras J. Patel, Celestine Chi, Hitendra M. Patel, “Water mediated TBAB catalyzed synthesis of spiro-indoline-pyrano[3,2-c]quinolines as α-amylase inhibitor and in silico studies”, Journal of Molecular Structure, 1273 (2023), 134305
Yuliya E. Ryzhkova, Varvara M. Kalashnikova, Michail N. Elinson, “6′-Amino-5,7-dibromo-2-oxo-3′-(trifluoromethyl)-1′H-spiro[indoline-3,4′-pyrano[2,3-c]pyrazole]-5′-carbonitrile”, Molbank, 2022:1 (2021), M1309
Pedro Brandão, Carolina S. Marques, Elisabete P. Carreiro, M. Pineiro, Anthony J. Burke, “Engaging Isatins in Multicomponent Reactions (MCRs) – Easy Access to Structural Diversity”, The Chemical Record, 21:4 (2021), 924
Majid Heravi, Vahideh Zadsirjan, Recent Advances in Applications of Name Reactions in Multicomponent Reactions, 2020, 139
Majid Heravi, Vahideh Zadsirjan, Recent Advances in Applications of Name Reactions in Multicomponent Reactions, 2020, 269
I. G. Mamedov, F. N. Naghiev, A. M. Maharramov, O. Uwangue, A. Farewell, P. Sunnerhagen, M. Erdelyi, “Antibacterial activity of 2-amino-3-cyanopyridine derivatives”, Mendeleev Commun., 30:4 (2020), 498–499
Zhenhang Xu, Yijun Du, Songxiang Wang, Zeru Wu, Yuhao Lou, Furen Zhang, “One‐pot Two‐step Reaction for Synthesis of Poly‐substituted Pyrano[3,2‐c]pyridones and Spiro[indoline‐3,4′‐pyrano[3,2‐c]pyridine]‐2,5′(6′H)‐diones in Water”, Journal of Heterocyclic Chem, 56:9 (2019), 2517
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
A. N. Vereshchagin, K. A. Karpenko, T. M. Iliyasov, M. N. Elinson, E. O. Dorofeeva, A. N. Fakhrutdinov, M. P. Egorov, “Diastereoselective multicomponent synthesis of (4RS,6SR)-4,6-diaryl-5,5-dicyano-2-methyl-1,4,5,6-tetrahydropyridine-3-carboxylates”, Russ Chem Bull, 67:11 (2018), 2049
A. N. Vereshchagin, K. A. Karpenko, M. N. Elinson, S. V. Gorbunov, Yu. E. Anisina, M. P. Egorov, “Stereoselective multicomponent synthesis of (2RS,6SR)-2,6-diaryl-3,3,5,5-tetracyanopiperidines”, Russ Chem Bull, 67:8 (2018), 1534
Vairaperumal Veeramani, Perumal Muthuraja, Sengodu Prakash, Muthiah Senthil Kumar, Antony Susaimanickam, Paramasivam Manisankar, “NbCl5‐Catalyzed One‐Pot Four Component Synthesis of Spiro Pyrazole and Benzo[7, 8]chromene Derivatives”, ChemistrySelect, 3:35 (2018), 10027
D. A. Tatarinov, V. I. Osipova, A. V. Bogdanov, R. R. Fayzullin, V. F. Mironov, “3-(4-Phosphoryl-4-methyl-2-oxopentyl)-3-hydroxyindolin-2-ones, the first phosphorus analogues of natural convolutamydines”, Mendeleev Commun., 28:3 (2018), 292–294
A. N. Vereshchagin, K. A. Karpenko, M. N. Elinson, E. O. Dorofeeva, A. S. Goloveshkin, M. P. Egorov, “Pseudo six-component stereoselective synthesis of 2,4,6-triaryl-3,3,5,5-tetracyanopiperidines”, Mendeleev Commun., 28:4 (2018), 384–386
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
A. N. Vereshchagin, “Classical and interdisciplinary approaches to the design of organic and hybrid molecular systems”, Russ Chem Bull, 66:10 (2017), 1765