References
- Pivovarenko, V. G.; Klueva, A. V.; Doroshenko, A. O.; Demchenko, A. P. Bands Separation in Fluorescence Spectra of Ketocyanine Dyes: Evidence for Their Complex Formation with Monohydric Alcohols. Chem. Phys. Lett. 2000, 325, 389–398. DOI: https://doi.org/10.1016/S0009-2614(00)00708-9.
- Das, P. K.; Pramanik, R.; Banerjee, D.; Bagchi, S. Studies of Solvation of Ketocyanine Dyes in Homogeneous and Heterogeneous Media by UV/Vis Spectroscopic Method. Spectrochim. Acta A 2000, 56, 2763–2773. DOI: https://doi.org/10.1016/S1386-1425(00)00321-8.
- Doroshenko, A. O.; Grigorovich, A. V.; Posokhov, E. A.; Pivovarenko, V. G.; Demchenko, A. P. Mol. Eng. 1998, 8, 199–215. DOI: https://doi.org/10.1023/A:1008393201193.
- Kawamata, J.; Inoue, K.; Inabe, T. Molecular and Crystal Structures of Novel Second-Order Nonlinear Optical Crystals: α, α′-Dibenzylidenecycloalkanones. Bcsj. 1998, 71, 2777–2786. DOI: https://doi.org/10.1246/bcsj.71.2777.
- Kaatz, P.; Shelton, D. P. Polarized Hyper‐Rayleigh Light Scattering Measurements of Nonlinear Optical Chromophores. J. Chem. Phys. 1996, 105, 3918–3929. DOI: https://doi.org/10.1063/1.472264.
- Kawamata, J.; Inoue, K.; Inabe, T.; Kiguchi, M.; Kato, M.; Taniguchi, Y. Large Second-Harmonic Generation Coefficients of Bis(Benzylidine) Cycloalkanones Estimated by the Second-Harmonic Wave Generated with the Evanescent Wave Technique. Chem. Phys. Lett. 1996, 249, 29–34. DOI: https://doi.org/10.1016/0009-2614(95)01373-3.
- Wu, J.; Shi, M.; Zhao, Y.; Wu, F. Two-Photon Absorption Property and Photopolymerization Sensitizing Efficiency of Asymmetrical Benzylidene Cyclopentanone Dyes. Dyes Pigm. 2008, 76, 690–695. DOI: https://doi.org/10.1016/j.dyepig.2007.01.007.
- Vatsadze, S. Z.; Gromov, S. P. Novel Linear Bis-Crown Receptors with Cross-Conjugated and Conjugated Central Cores. Mhc. 2017, 10, 432–445. DOI: https://doi.org/10.6060/mhc171142v.
- Li, G.; Zheng, Y.; Yao, J.; Hu, L.; Liu, Q.; Ke, F.; Feng, W.; Zhao, Y.; Yan, P.; He, W.; et al. Design and Green Synthesis of Piperlongumine Analogs and Their Antioxidant Activity against Cerebral Ischemia-Reperfusion Injury. ACS Chem. Neurosci. 2019, 10, 4545–4557. DOI: https://doi.org/10.1021/acschemneuro.9b00402.
- (a) Hasaninejad, A.; Zare, A.; Balooty, L.; Mehregan, H.; Shekouhy, M. Synth. Commun. 2010, 40, 3488–3495. (b) Wei, X.; Du, Z-Y.; Zheng, X.; Cui, X-X.; Conney, A. H.; Zhang, K. Eur. J. Med. Chem. 2012, 53, 235–245.
- (a) Rahman, A. F. M. M.; Ali, R.; Jahng, Y.; Kadi, A. A. Molecules 2012, 17, 571–583. (b) Kumar, S.; Kumar, P.; Makrandi, J. K. Der Chemica Sinica 2012, 3, 269–273.
- Karimi-Jaberi, Z.; Pooladian, B. A Facile Synthesis of α,α′-Bis(Substituted Benzylidene) Cycloalkanones Catalyzed by p -TSA under Solvent-Free Conditions. Green Chem. Let. Rev. 2012, 5, 187–193. DOI: https://doi.org/10.1080/17518253.2011.611478.
- (a) Deng, G.; Ren, T. Synth. Commun. 2003, 33, 2995–3001. (b) Li, J., Su W. Li, N. Synth. Commun. 2005, 35, 3037–3043. (c) Wang, L., Sheng J. Tian, H. Han, J. Fan, Z. Qian, C. Synthesis 2004, 18, 3060–3064.
- Li, J.; Yang, W.; Chen, G.; Li, T. A Facile Synthesis of α,α′- Bis (Substituted Benzylidene) Cycloalkanones Catalyzed by KF/Al 2 O 3 under Ultrasound Irradiation. Synth. Commun. 2003, 33, 2619–2625. DOI: https://doi.org/10.1081/SCC-120021982.
- Das, B.; Thirupathi, P.; Mahender, I.; Reddy, K. R. Convenient and Facile cross-Aldol Condensation Catalyzed by Molecular Iodine: An Efficient Synthesis of α,α′-Bis(Substituted-Benzylidene) Cycloalkanones. J. Mol. Catal. A: Chem. 2006, 247, 182–185. DOI: https://doi.org/10.1016/j.molcata.2005.11.044.
- (a) Amoozadeh, A.; Rahmani, S.; Nemati, F. S. Afr. J. Chem. 2000, 63, 72–74. (b) Tanemura, K.; Suzuki, T.; Nishida, Y.; Horaguchi, T. Chem. Lett. 2005, 34, 576–577. (c) Cao, Y-Q.; Dai, Z.; Zhang, R.; Chen, B-H. Synth. Commun. 2005, 35, 1045.
- (a) Jain, S. L.; Singhal, S.; Sain, B. PEG-Assisted Solvent and Catalyst Free Synthesis of 3,4-Dihydropyrimidinones under Mild Reaction Conditions. Green Chem. 2007, 9, 740–741. DOI: https://doi.org/10.1039/b702311a.
- (a) Rajeswari, M.; Sindhu, J.; Singh, H.; Khurana, J. M. RSC Ad. 2015, 5, 39686–39691. (b) Sindhu, J.; Singh, H.; Khurana, J. M. Mol. Divers. 2014, 18, 345–355.
- (a) Batalin, S.; Golikova, M.; Krustaleva, A.; Pchelintseva, N. Synth. Commun. 2020, 5, 659–668. (b) Batalim, S. D.; Golikova, M. A.; Khrustaleva, A. A.; Bakal, A. A.; Ponomareva, T. S.; Yu Goryacheva, I. ChemistrySelect 2021, 6, 11375–11380.
- Wang, X.; Gong, H.; Quan, Z.; Li, L.; Ye, H. One-Pot, Three-Component Synthesis of 1,4-Dihydropyridines in PEG-400. Synth. Commun. 2011, 41, 3251–3258. DOI: https://doi.org/10.1080/00397911.2010.517888.
- (a) Knölker, H.-J.; Baum, E.; Graf, R.; Jones, P. G.; Spieβ, O. Angew. Chem. Int. Ed. 1999, 38, 2583–2585. (b) Varshalomidze, I. E.; Golikov, A. G.; Krivenko, A. P. Chem. Heterocycl. Compd. 2009, 45, 1014–1016. (c) Vasilkova, N. O.; Kalugina, A. S.; Nikulin, A. V.; Krivenko, A. P. Russ. J. Org. Chem. 2019, 55, 995–998.
- Din, Z. U.; Trapp, M. A.; Soman de Medeiros, L.; Lazarin-Bidóia, D.; Garcia, F. P.; Peron, F.; Nakamura, C. V.; Rodríguez, I. C.; Wadood, A.; Rodrigues-Filho, E. Symmetrical and Unsymmetrical Substituted 2,5-Diarylidene Cyclohexanones as anti-Parasitic Compounds. Eur. J. Med. Chem. 2018, 155, 596–608. DOI: https://doi.org/10.1016/j.ejmech.2018.06.031.
- (a) Zoto, C. A.; Connors, R. E. J. Mol. Struct. 2010, 982, 121–126. (b) Zoto, C. A.; MacDonald, J. C. J. Mol. Struct. 2017, 1146, 458–466. DOI: https://doi.org/10.1016/j.molstruc.2010.08.016.
- Zhao, Y.; Wang, W.; Wu, F.; Zhou, Y.; Huang, N.; Gu, Y.; Zou, Q.; Yang, W. Polyethylene Glycol-Functionalized Benzylidene Cyclopentanone Dyes for Two-Photon Excited Photodynamic Therapy. Org. Biomol. Chem. 2011, 9, 4168–4175. DOI: https://doi.org/10.1039/c0ob01278e.
- Austin, M.; Egan, O. J.; Tully, R.; Pratt, A. C. Quinoline Synthesis: scope and Regiochemistry of Photocyclisation of Substituted Benzylidenecyclopentanone O-Alkyl and O-Acetyloximes. Org. Biomol. Chem. 2007, 5, 3778–3786. DOI: https://doi.org/10.1039/b711620a.
- (a) Kreher, U. P.; Rosamilia, A. E.; Raston, C. L.; Scott, J. L.; Strauss, C. R. Org. Lett. 2003, 5, 3107–3100. (b) Din, Z. U.; Rodrigues-Filho, E. Arab. J. Chem. 2016, 12, 4756–4763.
- Chen, J.; Spear, S. K.; Huddleston, J. G.; Rogers, R. D. Green Chem. 2005, 7, 64–82.