DBU-catalyzed synthesis of unsymmetrical cross-conjugated 2-arylidene-5-((dimethylamino)methylene)cyclopentanones

References

• Li, G.; Zheng, Y.; Yao, J.; Hu, L.; Liu, Q.; Ke, F.; Feng, W.; Zhao, Y.; Yan, P.; He, W.; et al. ACS Chem. Neurosci. 2019, 10, 4545–4557. DOI: 10.1021/acschemneuro.9b00402.
   PubMed Web of Science ®Google Scholar
• Zhao, Y.; Wang, W.; Wu, F.; Zhou, Y.; Huang, N.; Gu, Y.; Zou, Q.; Yang, W. Org. Biomol. Chem. 2011, 9, 4168–4175. DOI: 10.1039/c0ob01278e.
   PubMed Web of Science ®Google Scholar
• (a) Zoto, C. A.; Connors, R. E. J. Mol. Struct. 2010, 982, 121–126. DOI: 10.1016/j.molstruc.2010.08.016.
   Web of Science ®Google Scholar
  (b) Zoto, C. A.; MacDonald, J. C. J. Mol. Struct. 2017, 1146, 458–466. DOI: 10.1016/j.molstruc.2010.08.016.
   Web of Science ®Google Scholar
• (a) Gutrov, V. N.; Zakharova, G. V.; Nuriev, V. N.; Vatsadze, S. Z.; Gromov, S. P.; Chibisov, A. K. High Energy Chem. 2020, 54, 189–193. DOI: 10.1134/S0018143920030066.
   Web of Science ®Google Scholar
  (b) (Gutrov, V. N.; Zakharova, G. V.; Artsiusheuski, M. A.; Nuriev, V. N.; Vatsadze, S. Z.; Gromov, S. P.; Chibisov, A. K. High Energy Chem. 2019, 53, 198–203. DOI: 10.1134/S0018143919030056.
   Web of Science ®Google Scholar
  (c) (Doroshenko, A. O.; Sychevskaya, L. B.; Grygorovych, A. V.; Pivovarenko, V. G. J. Fluoresc. 2002, 12, 455–464. DOI: 10.1023/A:1021374212498.
   Web of Science ®Google Scholar
• (a) Knölker, H. J.; Baum, E.; Graf, R.; Jones, P. G.; Spieβ, O. Angew. Chem., Int. Ed. 1999, 38, 2853–2855.
   Web of Science ®Google Scholar
  (b) Vasilkova, N. O.; Kalugina, A. S.; Nikulin, A. V.; Krivenko, A. P. Russ. J. Org. Chem. 2019, 55, 995–998. DOI: 10.1134/S1070428019070145.
   Web of Science ®Google Scholar
• Austin, M.; Egan, O. J.; Tully, R.; Pratt, A. C. Org. Biomol. Chem. 2007, 5, 3778–3786. DOI: 10.1039/b711620a.
   PubMed Web of Science ®Google Scholar
• (a) 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. Eur. J. Med. Chem. 2018, 155, 596–608. DOI: 10.1016/j.ejmech.2018.06.031.
   PubMed Web of Science ®Google Scholar
  (b) Kreher, U. P.; Rosamilia, A. E.; Raston, C. L.; Scott, J. L.; Strauss, C. R. Org. Lett. 2003, 5, 3107–3110. DOI: 10.1021/ol0351145.
   PubMed Web of Science ®Google Scholar
  (c) Din, Z. U.; Rodrigues-Filho, E. Arab. J. Chem. 2019, 12, 4756–4763. DOI: 10.1016/j.arabjc.2016.09.014.
   Web of Science ®Google Scholar
• (a) Gümüş, M.; Koca, İ. ChemistrySelect 2020, 5, 12377–12397. DOI: 10.1002/slct.202002205.
   Web of Science ®Google Scholar
  (b) Abu-Shanab, F. A.; Sherif, S. M.; Mousa, S. A. S. J. Heterocyclic Chem. 2009, 46, 801–827. DOI: 10.1002/slct.202002205.
   Web of Science ®Google Scholar
• (a) Puyol, M.; Encinas, C.; Rivera, L.; Miltsov, S.; Alonso, J. Sens. Actuators B Chem. 2006, 115, 287–296. DOI: 10.1016/j.snb.2005.09.011.
   Web of Science ®Google Scholar
  (b) (Miltsov, S.; Encinas, C.; Alonso, J. Tetrahedron Lett. 2001, 42, 6129–6131. DOI: 10.1016/S0040-4039(01)01210-2.
   Web of Science ®Google Scholar
  (c) Yesudas, K.; Jemmis, E. D.; Bhanuprakash, K. Phys. Chem. Chem. Phys. 2015, 17, 12988–12999. DOI: 10.1039/C5CP01410G.
   PubMed Web of Science ®Google Scholar
• I. S. Martins, J. A. S. Coelho, MPs 2019, 2, 69. DOI: 10.3390/mps2030069.
   PubMedGoogle Scholar
• (a) Batalin, S.; Golikova, M.; Khrustaleva, A.; Pchelintseva, N. Synth. Commun. 2020, 50, 659–668. DOI: 10.1080/00397911.2019.1706182.
   Web of Science ®Google Scholar
  (b) Batalin, S. D.; Golikova, M. A.; Khrustaleva, A. A.; Bakal, A. A.; Ponomareva, T. S.; Goryacheva, I. Y. ChemistrySelect 2021, 6, 11375–11380. DOI: 10.1002/slct.202103128.
   Web of Science ®Google Scholar
  (c) Khrustaleva, A.; Batalin, S. Synth. Commun. 2022, 52, 787–793. DOI: 10.1080/00397911.2022.2056056.
   Web of Science ®Google Scholar
  (d) Batalin, S. Dyes Pigm. 2023, 208, 110850. DOI: 10.1016/j.dyepig.2022.110850.
   Google Scholar
• Boddu, S. K.; Ur Rehman, N.; Mohanta, T. K.; Majhi, A.; Avula, S. K.; Al-Harrasi, A. Green Chem. Let. Rev. 2022, 15, 765–795. DOI: 10.1080/17518253.2022.2132836.
   Web of Science ®Google Scholar
• (a) Al-Mousawi, S.; Abdel-Khalik, M. M.; El-Sherbiny, S.; John, E.; Elnagdi, M. H. J. Heterocycl. Chem. 2001, 38, 949–953. 201DOI: 10.1002/jhet.5570380422.
   Web of Science ®Google Scholar
  (b) Kumar, D.; Kommi, D. D.; Chopra, P.; Ansari, M. I.; Chakraborti, A. K. Eur. J. Org. Chem. 2012, 2012, 6407–6413. DOI: 10.1002/ejoc.201200778.
   Web of Science ®Google Scholar
• Connors, R. E.; Ucak-Astarlioglu, M. G. J. Phys. Chem. A 2003, 107, 7684–7691. DOI: 10.1021/jp0219597.
   Web of Science ®Google Scholar
• Palashuddin, S. M.; Chattopadhyay, A. RSC Adv. 2014, 4, 31994–31999. DOI: 10.1039/C4RA04264F.
   Web of Science ®Google Scholar
• Kellog, R. E.; Bennet, R. G. J. Chem. Phys. 1964, 41, 3042–3045.
   Web of Science ®Google Scholar