Эта публикация цитируется в 9 научных статьях (всего в 9 статьях)
Communications
A PASE-based approach towards 12-(1H-1,2,3-triazol-1-yl)-indolo[2,1-a]isoquinolines via the reaction of 3-(isoquinolin-1-yl)-1,2,4-triazines with benzyne
Аннотация:
12-(1H-1,2,3-Triazol-1-yl)indolo[2,1-a]isoquinolines are prepared in 51–56% yields using a PASE (pot, atom, step, economic)-based approach, namely, by the reaction between available 5-R-6-Ar-3-(isoquinolin-1-yl)-1,2,4-triazines and in situ generated benzyne. A mechanism comprising domino-transformation was suggested, and the structure of one key product was confirmed by a single crystal X-ray diffraction analysis.
Образец цитирования:
S. Gundala, M. R. Guda, A. F. Khasanov, D. S. Kopchuk, A. P. Krinochkin, S. Santra, G. V. Zyryanov, P. Venkatapuram, J. R. Garcia, V. N. Charushin, “A PASE-based approach towards 12-(1H-1,2,3-triazol-1-yl)-indolo[2,1-a]isoquinolines via the reaction of 3-(isoquinolin-1-yl)-1,2,4-triazines with benzyne”, Mendeleev Commun., 29:4 (2019), 369–371
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc1525
https://www.mathnet.ru/rus/mendc/v29/i4/p369
Эта публикация цитируется в следующих 9 статьяx:
A. Rammohan, A. P. Krinochkin, Yu. M. Sayfutdinova, Y. K. Shtaitz, S. S. Potapova, P. A. Slepukhin, V. S. Gaviko, D. S. Kopchuk, G. V. Zyryanov, O. N. Chupakhin, “Reaction of 6Н-5-(4-Fluorophenyl)-3-(2-pyridyl)-1,2,4-triazine with 4,5-Difluoro-1,2-dehydrobenzene”, Russ J Gen Chem, 94:9 (2024), 2255
M. R. Crampton, Organic Reaction Mechanisms Series, Organic Reaction Mechanisms 2019, 2023, 179
Zeinab A. Abdallah, Sherif M. H. Sanad, Ahmed E. M. Mekky, Mohamed S. Mohamed Ahmed, “New Arylazo‐Based (Chromene‐Thiazole) Hybrids as Potential MRSA Inhibitors”, Chemistry & Biodiversity, 20:4 (2023)
Wenyan Zhou, Jianbo Gan, Haiwen Li, Cunde Wang, “ZnCl2-Promoted Three-Component Reaction of 2-Aminochromenones, Aromatic Aldehydes, and Quinone Monoketals: Access to 5,6-Dihydro-12H-chromeno[2,3-c]isoquinolin-12-one Derivatives”, J. Org. Chem., 88:20 (2023), 14767
Rahimeh Hajinasiri, “A review of the synthesis of 1,2-dihydroisoquinoline, [2,1-a] isoquinoline and [5,1-a] isoquinoline since 2006”, Tetrahedron, 104 (2022), 132576
Guda Mallikarjuna Reddy, Vijaya Kumar Reddy Avula, Dmitry S. Kopchuk, Igor S. Kovalev, Grigory V. Zyryanov, Oleg N. Chupakhin, Jarem Raul Garcia, “Intramolecular oxazole-olefin Diels–Alder reactions: A review of the last two decades”, Synthetic Communications, 51:12 (2021), 1782
Yasuhiro Wada, Nobuhito Kurono, Hisanori Senboku, Kazuhiko Orito, “Synthesis of indolo[2,1‐a]isoquinolines by CF3COOH‐induced cyclization”, Journal of Heterocyclic Chem, 57:10 (2020), 3703
A. V. Shaferov, A. S. Malysheva, A. D. Averin, O. K. Grigorova, A. K. Buryak, I. P. Beletskaya, “Synthesis of optically active 3,3'-disubstituted biphenyl derivatives using palladium-catalyzed amination and their evaluation as enantioselective fluorescent detectors for amino alcohols and metal cations”, Russ Chem Bull, 69:7 (2020), 1366
G. V. Zyryanov, D. S. Kopchuk, I. S. Kovalev, S. Santra, M. Rahman, A. F. Khasanov, A. P. Krinochkin, O. S. Taniya, O. N. Chupakhin, V. N. Charushin, “Rational synthetic methods in creating promising (hetero)aromatic molecules and materials”, Mendeleev Commun., 30:5 (2020), 537–554