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Letters in Organic Chemistry

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ISSN (Print): 1570-1786
ISSN (Online): 1875-6255

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Mini-Review Article

Ionic Liquid: A Review on Multicomponent Synthesis of Dihydropyrano [3,2-c] Chromenes

Author(s): Kalpana M. Tekale, Santosh S. Katkar* and Diksha B. Wahul

Volume 20, Issue 10, 2023

Published on: 05 May, 2023

Page: [922 - 930] Pages: 9

DOI: 10.2174/1570178620666230309154227

Price: $65

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Abstract

The development of efficient and eco-friendly synthetic processes or techniques for the synthesis of heterocyclic compounds is increasing enormously. Here, an environmentally friendly ionic liquid is used as an efficient catalyst for the synthesis of biologically important dihydropyrano [3,2- c] chromenes. This is because ionic liquids play an important role in green chemistry due to their distinctive properties, easy handling, non-toxicity, increased reaction selectivity, and low solubility. This review focuses on dihydropyrano [3,2-c] chromenes synthesis due to their great importance as natural products, pharmaceuticals, and bioactive molecules. The review summarizes the application of ionic liquids as an effective catalyst for the multicomponent synthesis of dihydropyrano [3,2-c] chromene derivatives by using aromatic aldehydes, 4-hydroxycoumarin, and malononitrile in a green chemical manner.

Keywords: Ionic liquid, dihydropyorno [3, 2-c] chromene, multicomponent reaction, ecofriendly, heterocyclic compounds, heterocyclic compounds.

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[1]
Weber, L. Curr. Med. Chem., 2002, 9(23), 2085-2093.
[http://dx.doi.org/10.2174/0929867023368719] [PMID: 12470248]
[2]
Cimarelli, C. Molecules, 2019, 24(13), 2372-2373.
[http://dx.doi.org/10.3390/molecules24132372] [PMID: 31252514]
[3]
Younus, H.A.; Al-Rashida, M.; Hameed, A.; Uroos, M.; Salar, U.; Rana, S.; Khan, K.M. Expert Opin. Ther. Pat., 2021, 31(3), 267-289.
[http://dx.doi.org/10.1080/13543776.2021.1858797] [PMID: 33275061]
[4]
Inman, G.; Nlebedim, I.C.; Prodius, D. Energies, 2022, 15(2), 628-656.
[http://dx.doi.org/10.3390/en15020628]
[5]
Seddon, N.; Bearpark, T. Science, 2003, 302(5650), 1537-1540.
[http://dx.doi.org/10.1126/science.1089342] [PMID: 14593156]
[6]
Ye, Y.S.; Rick, J.; Hwang, B.J. J. Mater. Chem. A Mater. Energy Sustain., 2013, 1(8), 2719-2743.
[http://dx.doi.org/10.1039/C2TA00126H]
[7]
Marsh, K.N.; Boxall, J.A.; Lichtenthaler, R. Fluid Phase Equilib., 2004, 219(1), 93-98.
[http://dx.doi.org/10.1016/j.fluid.2004.02.003]
[8]
Yu, G.; Zhao, D.; Wen, L.; Yang, S.; Chen, X. AIChE J., 2012, 58(9), 2885-2899.
[http://dx.doi.org/10.1002/aic.12786]
[9]
Ratti, R. Adv. Chem. 1, 2014, 2014, 729842.
[http://dx.doi.org/10.1155/2014/729842]
[10]
Jain, S.; Rajguru, D.; Keshwal, B.S.; Acharya, A.D. ISRN Org. Chem., 2013, 2013, 1-5.
[http://dx.doi.org/10.1155/2013/185120]
[11]
Azarifar, D.; Nejat-Yami, R.; Sameri, F. Akrami. Z. Lett. Org. Chem., 2012, 9(6), 435-439.
[http://dx.doi.org/10.2174/157017812801322435]
[12]
Zendehdel, M.; Bodaghifard, M.A.; Behyar, H.; Mortezaei, Z. Microporous Mesoporous Mater., 2018, 266, 83-89.
[http://dx.doi.org/10.1016/j.micromeso.2018.02.052]
[13]
Jooya, A.; Davoodnia, A.; Fattahi, M.; Tavakoli-Hoseini, N. Org. Prep. Proced. Int., 2018, 50(6), 565-574.
[http://dx.doi.org/10.1080/00304948.2018.1537732]
[14]
Mobinikhaledi, A.; Moghanian, H. Souri. Z. Lett. Org. Chem., 2014, 11(6), 432-439.
[http://dx.doi.org/10.2174/1570178611666140304000656]
[15]
Mobinikhaledi, A.; Yazdanipour, A.; Ghashang, M. Green Process. Synth., 2016, 5, 289.
[16]
Nazemi Nasirmahale, L.; Goli Jolodar, O.; Shirini, F.; Tajik, H. Polycycl. Aromat. Compd., 2021, 41(1), 199-210.
[http://dx.doi.org/10.1080/10406638.2019.1576748]
[17]
Ren, Q.; Siau, W.Y.; Du, Z.; Zhang, K. Wang. J. Chemistry., 2011, 17(28), 7781-7785.
[http://dx.doi.org/10.1002/chem.201100927] [PMID: 21618299]
[18]
Patil, S.A.; Patil, S.A.; Patil, R. Future Med. Chem., 2015, 7(7), 893-909.
[http://dx.doi.org/10.4155/fmc.15.38] [PMID: 26061107]
[19]
Niknam, K.; Piran, A. Chem, 2013, 03, 1-8.
[20]
Mayank; Billing, B.K.; Agnihotri, P.K.; Kaur, N.; Singh, N.; Jang, D.K. ACS Sustain. Chem. Eng., 2018, 6(3), 3714-3743.
[http://dx.doi.org/10.1021/acssuschemeng.7b04048]
[21]
Mohammadi, R.; Esmati, S.; Gholamhosseini-Nazari, M.; Teimuri-Mofrad, R. J. Mol. Liq., 2019, 275, 523-534.
[http://dx.doi.org/10.1016/j.molliq.2018.11.042]
[22]
Shaterian, H.R.; Honarmand, M. Synth. Commun., 2011, 41(23), 3573-3581.
[http://dx.doi.org/10.1080/00397911.2010.519594]
[23]
Gong, K.; Wang, H-L.; Luo, J.; Liu, Z-L. J. Heterocycl. Chem., 2009, 46(6), 1145-1150.
[http://dx.doi.org/10.1002/jhet.193]
[24]
Wang, Y.; Ye, H.; Zuo, G.; Luo, J. J. Mol. Liq., 2015, 212, 418-422.
[http://dx.doi.org/10.1016/j.molliq.2015.09.030]
[25]
Bhagat, D.S.; Pande, S.G.; Katariya, M.V.; Pawar, R.P.; Kendrekar, P.S. Asian J. Chem., 2019, 31(4), 829-833.
[http://dx.doi.org/10.14233/ajchem.2019.21758]
[26]
Shahabi Nejad, M.; Sheibani, H. Catal. Lett., 2018, 148(1), 125-133.
[http://dx.doi.org/10.1007/s10562-017-2219-x]
[27]
Shaterian, H.R.; Oveisi, A.R. J. Indian Chem. Soc., 2011, 8(2), 545-552.
[http://dx.doi.org/10.1007/BF03249089]
[28]
Wang, Y.; Luo, J.; Xing, T.; Liu, Z. Monatsh. Chem., 2013, 144(12), 1871-1876.
[http://dx.doi.org/10.1007/s00706-013-1066-8]
[29]
Honarmand, M.; Tzani, A.; Detsi, A. J. Indian Chem. Soc., 2019, 16(3), 571-581.
[http://dx.doi.org/10.1007/s13738-018-1537-2]
[30]
Abaszadeh, M.; Seifi, M. Res. Chem. Intermed., 2015, 41(10), 7715-7723.
[http://dx.doi.org/10.1007/s11164-014-1855-7]
[31]
Shaikh, M.A.; Farooqui, M.; Abed, S. Res. Chem. Intermed., 2019, 45(3), 1595-1617.
[http://dx.doi.org/10.1007/s11164-018-3696-2]
[32]
Teimuri-Mofrad, R.; Esmati, S.; Tahmasebi, S.; Gholamhosseini-Nazari, M. J. Organomet. Chem., 2018, 870, 38-50.
[http://dx.doi.org/10.1016/j.jorganchem.2018.06.007]
[33]
Fadavipoor, E.; Badri, R.; Kiasat, A.; Sanaeishoar, H. Polycycl. Aromat. Compd., 2020, 40(4), 1084-1096.
[http://dx.doi.org/10.1080/10406638.2018.1526809]
[34]
Tavakoli-Hoseini, N.; Heravi, M.M.; Bamoharram, F.F.; Davoodnia, A. Asian J. Chem., 2011, 23, 3599-3601.
[35]
Davarpanah, J.; Kiasat, A.R.; Noorizadeh, S.; Ghahremani, M. J. Mol. Catal. Chem., 2013, 376, 78-89.
[http://dx.doi.org/10.1016/j.molcata.2013.04.020]
[36]
Mansouri, N.; Baghery, S.; Zolfigol, M.A. Nano Res., 2018, 3(2), 170-177.
[37]
Zheng, J.; Li, Y. Mendeleev Commun., 2011, 21(5), 280-281.
[http://dx.doi.org/10.1016/j.mencom.2011.09.017]
[38]
Khaligh, N.G.; Mihankhah, T.; Johan, M.R. J. Mol. Liq., 2019, 277, 794-804.
[http://dx.doi.org/10.1016/j.molliq.2019.01.024]
[39]
Ghorbani-Vaghei, R.; Mahmoodi, J.; Maghbooli, Y. Curr. Org. Synth., 2017, 14, 904-911.
[http://dx.doi.org/10.2174/1570179414666170203150629]
[40]
Shaabani, A.; Samadi, S.; Badri, Z.; Rahmati, A. Catal. Lett., 2005, 104(1-2), 39-43.
[http://dx.doi.org/10.1007/s10562-005-7433-2]
[41]
Shaterian, H.R.; Arman, M.; Rigi, F. J. Mol. Liq., 2011, 158(2), 145-150.
[http://dx.doi.org/10.1016/j.molliq.2010.11.010]

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