[1] Kaur, M., Kaur, M., Bandopadhyay, T., Sharma, A., Priya, A., Singh, A., & Banerjee, B. (2023). Naturally occurring, natural product inspired and synthetic heterocyclic anti-cancer drugs.
Physical Sciences Reviews,
8(10), 3393-3446.
https://doi.org/10.1515/ psr-2022-0003
[2] Hinkle, J. L., & Cheever, K. H. (2013).
Study guide for Brunner & Suddarth's textbook of medical-surgical nursing (13 ed.). Lippincott Williams & Wilkins.
https://books.go ogle.com/books/about/Study_Guide_for_Brunner_Suddarth_s_Textb.html?id=peCdAgAAQBAJ
[3] Abd-Ellah, H. S., Abdel-Aziz, M., Shoman, M. E., Beshr, E. A. M., Kaoud, T. S., & Ahmed, A-S. F. F. (2016). Novel 1,3,4-oxadiazole/oxime hybrids: Synthesis, docking studies and investigation of anti-inflammatory, ulcerogenic liability and analgesic activities.
Bioorganic Chemistry,
69, 48-63.
https://doi.org/10.1016/j.bioorg.2016.09.005
[4] Al-Issa, S. A. (2013). Synthesis and anticancer activity of some fused pyrimidines and related heterocycles.
Saudi Pharmaceutical Journal,
21(3), 305-316.
https://doi.org/10.101 6/j.jsps.2012.09.002
[5] Banik, B. K., Banerjee, B., Kaur, G., Saroch, S., & Kumar, R. (2020). Tetrabutylammonium Bromide (TBAB) Catalyzed Synthesis of Bioactive Heterocycles.
Molecules,
25(24), 5918.
https://doi.org/10.3390/molecules25245918
[6] Gaikwad, D. D., Chapolikar, A. D., Devkate, C. G., Warad, K. D., Tayade, A. P., Pawar, R. P., & Domb, A. J. (2015). Synthesis of indazole motifs and their medicinal importance: An overview.
European Journal of Medicinal Chemistry,
90(12), 707-731.
https://d oi.org/10.1016/j.ejmech.2014.11.029
[7] Chabukswar, A. R., Kuchekar, B. S., Jagdale, S. C., Lokhande, P. D., Chabukswar, V. V., Shisodia, S. U., Mahabal, R. H., Londhe, A. M., & Ojha, N. S. (2016). Synthesis and evaluation of analgesic, anti-asthmatic activity of (E)-1-(8-hydroxyquinolin-7-yl)-3-phenylprop-2-en-1 ones.
Arabian Journal of Chemistry,
9(5), 704-712.
https://doi. org/10.1016/j.arabjc.2014.10.046
[8] Banerjee, B. (2017). Recent developments on ultrasound-assisted one-pot multicomponent synthesis of biologically relevant heterocycles.
Ultrasonics Sonochemistry,
35, 15-35.
https://doi.org/10.1016/j.ultsonch.2016.10.010
[9] Su, B., Cai, C., Deng, M., Liang, D., Wang, L., & Wang, Q. (2014). Design, synthesis, antiviral activity, and SARs of 13a-substituted phenanthroindolizidine alkaloid derivatives.
Bioorganic & Medicinal Chemistry Letters,
24(13), 2881-2884.
https://doi.org/10.1 016/j.bmcl.2014.04.101
[10] Banerjee, B. (2017). Recent developments on nano-ZnO catalyzed synthesis of bioactive heterocycles.
Journal of Nanostructure in Chemistry,
7(4), 389-413.
https://doi.org/ 10.1007/s40097-017-0247-0
[11] Kaur, G., Devi, M., Kumari, A., Devi, R., & Banerjee, B. (2018). One-Pot Pseudo Five Component Synthesis of Biologically Relevant 1,2,6-Triaryl-4-arylamino-piperidine-3-ene-3- carboxylates: A Decade Update.
ChemistrySelect,
3(34), 9892-9910.
https: //doi.org/10.1002/slct.201801887
[12] Kaur, G., Devi, P., Thakur, S., Kumar, A., Chandel, R., & Banerjee, B. (2019). Magnetically separable transition metal ferrites: versatile heterogeneous nano‐catalysts for the synthesis of diverse bioactive heterocycles.
ChemistrySelect,
4(7), 2181-2199.
https://doi.org/ 10.1002/slct.201803600
[13] Kaur, G., Sharma, A., & Banerjee, B. (2018). [Bmim] PF6: An efficient tool for the synthesis of diverse bioactive heterocycles.
Journal of the Serbian Chemical Society,
83(10), 1071-1097.
https://doi.org/10.2298/JSC180103052K
[14] Sharma, A., Priya, A., Kaur, M., Singh, A., Kaur, G., & Banerjee, B. (2021). Ultrasound-assisted synthesis of bioactive S-heterocycles.
Synthetic Communications,
51(21), 3209-3236.
https://doi.org/10.1080/00397911.2021.1970775
[15] Banerjee, B. (2019). Ultrasound and Nano‐Catalysts: An Ideal and Sustainable Combination to Carry out Diverse Organic Transformations.
ChemistrySelect,
4(8), 2484-2500.
h ttps://doi.org/10.1002/slct.201803081
[16] Hu, X., & Yip, A. C. K. (2021). Heterogeneous Catalysis: Enabling a Sustainable Future.
Frontiers in Catalysis,
1, 667675.
https://doi.org/10.3389/fctls.2021.667675
[17] Bavykina, A., Kolobov, N., Khan, I. S., Bau, J. A., Ramirez, A., & Gascon, J. (2020). Metal–Organic Frameworks in Heterogeneous Catalysis: Recent Progress, New Trends, and Future Perspectives.
Chemical Reviews,
120(16), 8468-8535.
https://doi.org/10.102 1/acs.chemrev.9b00685
[18] Dang, S., Yang, H., Gao, P., Wang, H., Li, X., Wei, W., & Sun, Y. (2019). A review of research progress on heterogeneous catalysts for methanol synthesis from carbon dioxide hydrogenation.
Catalysis Today,
330, 61-75.
https://doi.org/10.1016/j.cattod.2018.0 4.021
[19] Israf Ud, D., Nasir, Q., Garba, M. D., Alharthi, A. I., Alotaibi, M. A., & Usman, M. (2022). A Review of Preparation Methods for Heterogeneous Catalysts.
Mini-Reviews in Organic Chemistry,
19(1), 92-110.
https://doi.org/10.2174/1570193X18666210308151136
[20] Jambhulkar, D. K., Ugwekar, R. P., Bhanvase, B. A., & Barai, D. P. (2022). A review on solid base heterogeneous catalysts: preparation, characterization and applications.
Chemical Engineering Communications,
209(4), 433-484.
https://doi.org/10.1080/00986445. 2020.1864623
[21] Palma, V., Barba, D., Cortese, M., Martino, M., Renda, S., & Meloni, E. (2020). Microwaves and Heterogeneous Catalysis: A Review on Selected Catalytic Processes.
Catalysts,
10(2), 246.
https://doi.org/10.3390/catal10020246
[22] Wang, A., Li, J., & Zhang, T. (2018). Heterogeneous single-atom catalysis.
Nature Reviews Chemistry,
2(6), 65-81.
https://doi.org/10.1038/s41570-018-0010-1
[23] Firouzabadi, H., & Jafari, A. A. (2005). Heteropoly acids, their salts and polyoxometalates as heterogenous, efficient and eco-friendly catalysts in organic reactions: Some recent advances.
Journal of the Iranian Chemical Society,
2(2), 85-114.
https://doi.org/10. 1007/BF03247201
[24] Heravi, M. M., & Sadjadi, S. (2009). Recent developments in use of heteropolyacids, their salts and polyoxometalates in organic synthesis.
Journal of the Iranian Chemical Society,
6(1), 1-54.
https://doi.org/10.1007/BF03246501
[25] Thomas, J. M., & Zamaraev, K. I. (1992).
Perspective in Catalysis. Blackwell Scientific Publications.
https://search.worldcat.org/title/perspectives-in-catalysis/oclc/22907850
[26] Pope, M. T., & Müller, A. (1991). Polyoxometalate Chemistry: An Old Field with New Dimensions in Several Disciplines.
Angewandte Chemie International Edition in English,
30(1), 34-48.
https://doi.org/10.1002/anie.199100341
[27] Illingworth, J. W., & Keggin, J. F. (1935). 127. Identification of the 12-heteropoly-acids and their salts by means of X-ray powder photographs.
Journal of the Chemical Society 575-580.
https://doi.org/10.1039/JR9350000575
[28] Mbomekalle, I-M., Lu, Y. W., Keita, B., & Nadjo, L. (2004). Simple, high yield and reagent-saving synthesis of pure α-K
6P
2W
18O
62·14H
2O.
Inorganic Chemistry Communications,
7(1), 86-90.
https://doi.org/10.1016/j.inoche.2003.10.011
[29] Venturello, C., D'aloisio, R., Bart, J. J., & Ricci, M. (1985). A new peroxotungsten heteropoly anion with special oxidizing properties: synthesis and structure of tetrahexylammonium tetra (dipewroxotungsto) phosphate (3-).
Journal of molecular catalysis,
32(1), 107-110.
https://doi.org/10.1016/0304-5102(85)85037-9
[30] Priya, A., Sharma, A., Kaur, M., Singh, A., & Banerjee, B. (2022). Preyssler catalyst: a heterogeneous polyacidic catalyst for the efficient synthesis of diverse bioactive heterocyclic scaffolds.
Arkivoc,
2022(3), 85-111.
https://doi.org/10.24820/ark.5550 190.p011.783
[31] Bamoharram, F., Heravi, M., Ardalan, P., & Ardalan, T. (2010). A kinetic study of the esterification of lactic acid by ethanol in the presence of Preyssler acid an eco-friendly solid acid catalyst.
Reaction Kinetics, Mechanisms and Catalysis,
100(1), 71-78.
htt ps://doi.org/10.1007/s11144-010-0159-1
[32] Kim, J. K., Choi, J. H., Park, D. R., & Song, I. K. (2013). Etherification of n-Butanol to Di-n-Butyl Ether Over Keggin-, Wells-Dawson-, and Preyssler-Type Heteropolyacid Catalysts.
Journal of Nanoscience and Nanotechnology,
13(12), 8121-8126.
https:// doi.org/10.1166/jnn.2013.8178
[33] Hafizi, A., Ahmadpour, A., Heravi, M. M., Bamoharram, F. F., & Khosroshahi, M. (2012). Alkylation of Benzene with 1-Decene Using Silica Supported Preyssler Heteropoly Acid: Statistical Design with Response Surface Methodology.
Chinese Journal of Catalysis,
33(2-3), 494-501.
https://doi.org/10.1016/S1872-2067(11)60357-4
[34] Bamoharram, F. F., Heravi, M. M., & Mehdizadeh, S. (2009). Preyssler Anion as a Green and Eco-friendly Catalyst for Photocatalytic Oxidation of Aromatic Aldehydes.
Synthesis and Reactivity in Inorganic, Metal-Organic, and Nano-Metal Chemistry,
39(10), 746-750.
https://doi.org/10.1080/15533170903433287
[35] Bamoharram, F. F., Heravi, M. M., Roshani, M., & Tavakoli, N. (2006). N-oxidation of pyridine carboxylic acids using hydrogen peroxide catalyzed by a green heteropolyacid catalyst: Preyssler's anion, [NaP5W30O110]
14−.
Journal of Molecular Catalysis A: Chemical,
252(1-2), 219-225.
https://doi.org/10.1016/j.molcata.2006.02.059
[36] Romanelli, G., Ruiz, D., Vázquez, P., Thomas, H., & Autino, J. C. (2010). Preyssler heteropolyacid H14[NaP5W29MoO110]: A heterogeneous, green and recyclable catalyst used for the protection of functional groups in organic synthesis.
Chemical Engineering Journal,
161(3), 355-362.
https://doi.org/10.1016/j.cej.2009.12.029
[37] Bamoharram, F. F., Heravi, M. M., Roshani, M., Gharib, A., & Jahangir, M. (2006). A catalytic method for synthesis of γ-butyrolactone, ɛ-caprolactone and 2-cumaranone in the presence of Preyssler's anion, [NaP5W30O110]14−, as a green and reusable catalyst.
Journal of Molecular Catalysis A: Chemical,
252(1-2), 90-95.
https://doi.o rg/10.1016/j.molcata.2006.01.067
[38] Bamoharram, F. F., Heravi, M. M., Roshani, M., Gharib, A., & Jahangir, M. (2007). Catalytic Method for Synthesis of Aspirin by a Green, Efficient and Recyclable Solid Acid Catalyst (Preyssler's Anion) at Room Temperature.
Journal of the Chinese Chemical Society,
54(4), 1017-1020.
https://doi.org/10.1002/jccs.200700146
[39] Heravi, M. M., Bamoharram, F. F., Rajabzadeh, G., Seifi, N., & Khatami, M. (2006). Preyssler heteropolyacid [NaP
5W
30O
110]
14−, as a new, green and recyclable catalyst for the synthesis of [1,2,4]triazino[4,3-b][1,2,4,5]tetrazines.
Journal of Molecular Catalysis A: Chemical,
259(1-2), 213-217.
https://doi.org/10.1016/j.molcata.2006.06.037
[40] Azarifar, D., Khatami, S-M., Zolfigol, M. A., & Sheikh, D. (2013). Nano TiO2-supported Preyssler-type heteropolyacid (nanoTiO
2/H
14[NaP
5W
30O
110]): an efficient and re-usable catalyst for the one-pot synthesis of N-acetyl-2-aryl-1,2-dihydro-(4H)-3,1-benzoxazin-4-ones.
Journal of the Iranian Chemical Society,
10(5), 1039-1046.
http s://doi.org/10.1007/s13738-013-0242-4
[41] Heravi, M. M., Nahavandi, F., Sadjadi, S., Oskooie, H. A., & Bamoharram, F. F. (2010). Efficient Synthesis of Bis-Coumarins Using Silica-Supported Preyssler Nanoparticles.
Synthetic Communications,
40(4), 498-503.
https://doi.org/10.1080/003979109029 85556
[42] Nazari, H., Ahmadpour, A., Bamoharram, F. F., Heravi, M. M., & Eslami, N. (2012). Comparison of Catalysts Preyssler and Silica-Supported Nano Preyssler in the Synthesis of Acetyl Salicylic Acid.
Journal of Chemistry,
9(1), 892861.
https://doi.org/10.115 5/2012/892861
[43] Wu, S., Zhang, W., Wang, J., & Ren, X. (2008). Preyssler-Structured Tungstophosphoric Acid Catalyst on Functionalized Silica for Esterification of n-Butanol with Acetic Acid.
Catalysis Letters,
123(3), 276-281.
https://doi.org/10.1007/s10562-008-9419-3
[44] Hafizi, A., Ahmadpour, A., Heravi, M. M., & Bamoharram, F. F. (2014). The Application of Silica-Supported Preyssler HPA as a Heterogeneous and Green Catalyst for the Alkylation of Benzene.
Petroleum Science and Technology,
32(9), 1022-1027.
https ://doi.org/10.1080/10916466.2011.637534
[45] Bamoharram, F. F., Heravi, M. M., Roushani, M., Toosi, M. R., & Jodeyre, L. (2009). Synthesis and characterization of silica-supported Preyssler nano particles and its catalytic activity for photodegradation of methyl orange.
Green Chemistry Letters and Reviews,
2(1), 35-41.
https://doi.org/10.1080/17518250902998095
[46] Bamoharram, F. F., Heravi, M. M., Teymouri, H., Zebarjad, M., & Ahmadpour, A. (2011). Preyssler Heteropolyacid Supported on Nano-SiO2: A Green and Reusable Catalyst in Selective Oxidation of Benzyl Alcohols to Benzaldehydes.
Synthesis and Reactivity in Inorganic, Metal-Organic, and Nano-Metal Chemistry,
41(10), 1221-1228.
https: //doi.org/10.1080/15533174.2011.591873
[47] Heravi, M. M., Tavakoli-Hoseini, N., & Bamoharram, F. F. (2010). Silica-supported Preyssler nano particles: a green, reusable and highly efficient heterogeneous catalyst for the synthesis of carbamatoalkyl naphthols.
Green Chemistry Letters and Reviews,
3(4), 263-267.
https://doi.org/10.1080/17518251003749387
[48] Saneinezhad, S., Mohammadi, L., Zadsirjan, V., Bamoharram, F. F., & Heravi, M. M. (2020). Silver nanoparticles-decorated Preyssler functionalized cellulose biocomposite as a novel and efficient catalyst for the synthesis of 2-amino-4
H-pyrans and spirochromenes.
Scientific Reports,
10(1), 14540.
https://doi.org/10.1038/s41598-020-70738-z
[49] Azarifar, D., Khatami, S-M., & Najminejad, Z. (2014). Ultrasound-accelerated selective oxidation of primary aromatic amines to azoxy derivatives with trans-3,5-dihydroperoxy-3,5-dimethyl-1,2-dioxolane catalyzed by Preyssler acid-mediated nano-TiO2.
Journal of the Iranian Chemical Society,
11(2), 587-592.
https://doi.org/10.1007/s13738-01 3-0328-z
[50] Azarifar, D., Khatami, S-M., & Nejat-Yami, R. (2014). Nano-titania-supported Preyssler-type heteropolyacid: An efficient and reusable catalyst in ultrasound-promoted synthesis of 4H-chromenes and 4H-pyrano[2,3-c]pyrazoles.
Journal of Chemical Sciences,
126(1), 95-101.
https://doi.org/10.1007/s12039-013-0548-x
[51] Azarifar, D., Khatami, S-M., Zolfigol, M. A., & Nejat-Yami, R. (2014). Nano-titania sulfuric acid-promoted synthesis of tetrahydrobenzo[b]pyran and 1,4-dihydropyrano[2,3-c]pyrazole derivatives under ultrasound irradiation.
Journal of the Iranian Chemical Society,
11(4), 1223-1230.
https://doi.org/10.1007/s13738-013-0392-4
[52] Khalaj, M., Farahani, N., Sadeghpour, M., Rajabzadeh, H., & Khatami, S. M. (2018). PEG/ZnBr2-Assisted Multicomponent Reactions: A Novel Procedure for the Synthesis of Functionalized 5, 6-Dihydropyran-2-ones.
Synlett,
29(07), 894-897.
https://doi.or g/10.1055/s-0036-1591760
[53] Khalaj, M., Sadeghpour, M., Mousavi Safavi, S. M., Lalegani, A., & Khatami, S. M. (2019). Copper-catalyzed synthesis of thiazolidine derivatives via multicomponent reaction of terminal alkynes, elemental sulfur, and aziridines.
Monatshefte für Chemie - Chemical Monthly,
150(6), 1085-1091.
https://doi.org/10.1007/s00706-019-2363-7
