References
- Deng, G.; Wang, Q.; Yang, M.; Li, B.; Han, T.; Chang, B.; Li, X.; Zhang, X.; Li, Z. Synthesis and Modifications of Electron-Withdrawing Groups Based on Multi-Cyano Heterocyclics. Mini-Rev. Org. Chem. 2019, 16, 208–215. DOI: 10.2174/1570193X15666180412151523.
- Li, M.; Li, Y.; Zhang, H.; Wang, S.; Ao, Y.; Cui, Z. Molecular Engineering of Organic Chromophores and Polymers for Enhanced Bulk Second-Order Optical Nonlinearity. J. Mater. Chem. C. 2017, 5, 4111–4122. DOI: 10.1039/C7TC00713B.
- Cho, M. J.; Choi, D. H.; Sullivan, P. A.; Akelaitis, A. J. P.; Dalton, L. R. Recent Progress in Second-Order Nonlinear Optical Polymers and Dendrimers. Prog. Polym. Sci. 2008, 33, 1013–1058. DOI: 10.1016/j.progpolymsci.2008.07.007.
- Redon, S.; Eucat, G.; Ipuy, M.; Jeanneau, E.; Gautier-Luneau, I.; Ibanez, A.; Andraud, C.; Bretonnière, Y. Tuning the Solid-State Emission of Small Push-Pull Dipolar Dyes to the Far-Red through Variation of the Electron-Acceptor Group. Dyes Pigm. 2018, 156, 116–132. DOI: 10.1016/j.dyepig.2018.03.049.
- Belikov, M.; Yu Ievlev, M.; Yu Fedoseev, S. V.; Ershov, O. V. Tuning the Photochromic Properties of Chromophores Containing a Nitrile-Rich Acceptor: A Novel Branch in the Investigation of Negative Photochromes. New J. Chem. 2019, 43, 8414–8417. DOI: 10.1039/C9NJ01648A.
- Dhondge, A. P.; Chen, J.-Y.; Lin, T.; Yen, F.-M.; Li, K.-W.; Hsieh, H.-C.; Kuo, M.-Y. Di-2-(2-Oxindolin-3-Ylidene)Malononitrile Derivatives for N-Type Air-Stable Organic Field-Effect Transistors. Org. Lett. 2018, 20, 40–43. DOI: 10.1021/acs.orglett.7b03284.
- Dhondge, A. P.; Tsai, P.-C.; Nien, C.-Y.; Xu, W.-Y.; Chen, P.-M.; Hsu, Y.-H.; Li, K.-W.; Yen, F.-M.; Tseng, S.-L.; Chang, Y.-C.; et al. Angular-Shaped Naphthalene Bis(1,5-Diamide-2,6-Diylidene)Malononitrile for High-Performance, Air-Stable N-Type Organic Field-Effect Transistors. Org. Lett. 2018, 20, 2538–2542. DOI: 10.1021/acs.orglett.8b00684.
- Dhondge, A. P.; Huang, Y.-X.; Lin, T.; Hsu, Y.-H.; Tseng, S.-L.; Chang, Y.-C.; Chen, H. J. H.; Kuo, M.-Y. Benzodipyrrole-2,6-Dione-3,7-Diylidenedimalononitrile Derivatives for Air-Stable n-Type Organic Field-Effect Transistors: Critical Role of N-Alkyl Substituent on Device Performance. J. Org. Chem. 2019, 84, 14061–14068. DOI: 10.1021/acs.joc.9b02207.
- Zhao, D.; Hu, J.; Liu, Z.; Xiao, B.; Wang, X.; Zhou, E.; Zhang, Q. Isatylidene Malononitrile Derived Acceptors for Fullerene Free Organic Solar Cells. Dyes Pigm. 2018, 151, 102–109. DOI: 10.1016/j.dyepig.2017.12.054.
- Zhao, D.; Hu, J.; Cao, K.; Xiao, B.; Zhou, E.; Zhang, Q. Isatin-Derived Non-Fullerene Acceptors towards High Open Circuit Voltage Solar Cells. Dyes Pigm. 2019, 162, 898–904. DOI: 10.1016/j.dyepig.2018.11.027.
- Chen, R.; Zhang, G.; Zhou, W. CN Patent 110790776, 2020.
- El-Sharief, A. M.; Sh.; Ammar, Y. A.; Belal, A.; El-Sharief, M. A. M.; Sh.; Mohamed, Y. A.; Mehany, A. B. M.; Elhag Ali, G. A. M.; Ragab, A. Design, Synthesis, Molecular Docking and Biological Activity Evaluation of Some Novel Indole Derivatives as Potent Anticancer Active Agents and Apoptosis Inducers. Bioorg. Chem. 2019, 85, 399–412. DOI: 10.1016/j.bioorg.2019.01.016.
- Salem, M. A.; Ragab, A.; Askar, A. A.; El-Khalafawy, A.; Makhlouf, A. H. Design, Synthesis, Molecular Docking and Biological Activity Evaluation of Some Novel Indole Derivatives as Potent Anticancer Active Agents and Apoptosis Inducers. Eur. J. Med. Chem. 2020, 188, 111977. DOI: 10.1016/j.ejmech.2019.111977.
- El-Gaby, M. S. A.; El-Hag Ali, G. A. M.; El-Maghraby, A. A.; Abd El-Rahman, M. T.; Helal, M. H. M. Synthesis, Characterization and in Vitro Antimicrobial Activity of Novel 2-Thioxo-4-Thiazolidinones and 4,4'-bis(2-Thioxo-4-Thiazolidinone-3-yl)Diphenylsulfones. Eur. J. Med. Chem. 2009, 44, 4148–4152. DOI: 10.1016/j.ejmech.2009.05.005.
- Chu, W.; Rothfuss, J.; Zhou, D.; Mach, R. H. Synthesis and Evaluation of Isatin Analogs as Caspase-3 Inhibitors: Introduction of a Hydrophilic Group Increases Potency in a Whole Cell Assay. Bioorg. Med. Chem. Lett. 2011, 21, 2192–2197. DOI: 10.1016/j.bmcl.2011.03.015.
- Chu, W.; Rothfuss, J.; Avignon, A.; Zeng, C.; Zhou, D.; Hotchkiss, R. S.; Mach, R. H. Isatin Sulfonamide Analogs Containing a Michael Addition Acceptor: A New Class of Caspase 3/7 Inhibitors. J. Med. Chem. 2007, 50, 3751–3755. DOI: 10.1021/jm070506t.
- Belikov, M.; Yu. Ievlev, M.; Yu Milovidova, A. G.; Ershov, O. V. Synthesis of 2-(5-Aryl-4-Methyl-2-Oxo-1,2-Dihydro-3H-Pyrrol-3-Ylidene)Malononitriles. Russ. J. Org. Chem. 2017, 53, 1601–1603. DOI: 10.1134/S1070428017100207.
- Milovidova, A. G.; Belikov, M.; Yu.; Ievlev, M.; Yu.; Ershov, O. V.; Nasakin, O. E.; Tafeenko, V. A. Pyrrole Ring Opening – Pyridine Ring Closure: Recyclization of 2-(2-Oxo-1,2-Dihydro-3H-Pyrrol-3-Ylidene)Malononitriles into Highly Functionalized Nicotinonitriles. Tetrahedron Lett. 2020, 61, 151368. DOI: 10.1016/j.tetlet.2019.151368..
- Milovidova, A. G.; Belikov, M.; Yu. Ievlev, M.; Yu Ershov, O. V.; Nasakin, O. E. Reaction of 2-(2-Oxo-1,2-Dihydro-3H-Pyrrol-3-Ylidene)Malononitriles with C-Nucleophiles. Synthesis of New Spiro-Fused Pyrrole Derivatives. Russ. J. Org. Chem. 2018, 54, 1790–1793. DOI: 10.1134/S1070428018120084.
- Ievlev, M.; Yu. Ershov, O. V.; Milovidova, A. G.; Belikov, M.; Yu. Nasakin, O. E. A Novel Method for the Domino Synthesis of 6-Imino-2,7-Dioxabicyclo[3.2.1]Octane-4,4,5-Tricarbonitriles and Studies of Stereochemical Characteristics of Formation and Structure Thereof. Chem. Heterocyc. Comp. 2015, 5, 457–461. DOI: 10.1007/s10593-015-1720-7.
- Ievlev, M.; Yu.; Ershov, O. V.; Milovidova, A. G.; Belikov, M.; Yu.; Vasil’ev, A. N.; Tafeenko, V. A. A New Branch of the Diversity-Oriented Synthesis Based on 4-Oxoalkane-1,1,2,2-Tetracarbonitriles: Synthesis of Cyano-Substituted Iminofuran Derivatives. Russ. J. Org. Chem. 2018, 54, 1337–1340. DOI: 10.1134/S1070428018090129.
- Ievlev, M.; Yu.; Ershov, O. V.; Belikov, M.; Yu.; Milovidova, A. G.; Tafeenko, V. A.; Nasakin, O. E. Diastereoselective Synthesis of 3,4-Dihydro-2H-Pyran-4-Carboxamides through an Unusual Regiospecific Quasi-Hydrolysis of a Cyano Group. Beilstein J. Org. Chem. 2016, 12, 2093–2098. DOI: 10.3762/bjoc.12.198.
- Crystallographic data (excluding structure factors) for the structure 6 in this paper have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication number CCDC 2033762. Copies of the data can be obtained free of charge from The Cambridge Crystallographic Data Centre via. https://www.ccdc.cam.ac.uk/structures/.
- Sheldrick, G. M. A Short History of SHELX. Acta Crystallogr. A. 2008, 64, 112–122. DOI: 10.1107/s0108767307043930.