References
- Banerjee, B. Recent Developments on Ultrasound-Assisted Synthesis of Bioactive N-Heterocycles at Ambient Temperature. Aust. J. Chem 2017, 70, 872–888. DOI: https://doi.org/10.1071/CH17080.
- Banerjee, B. Recent Developments on Nano-ZnO Catalyzed Synthesis of Bioactive Heterocycles. J. Nanostruct Chem 2017, 7, 389–413. DOI: https://doi.org/10.1007/s40097-017-0247-0.
- Kaur, M.; Kaur, M.; Bandopadhyay, T.; Sharma, A.; Priya, A.; Singh, A.; Banerjee, B. Naturally Occurring, Natural Product Inspired and Synthetic Heterocyclic anti-Cancer Drugs. Phys. Sci. Rev 2022, in press, DOI: https://doi.org/10.1515/psr-2022-0003.
- Kaur, G.; Sharma, A.; Banerjee, B. [Bmim] PF6: An Efficient Tool for the Synthesis of Diverse Bioactive Heterocycles. J. Serb. Chem. Soc. 2018, 83, 1071–1097. DOI: https://doi.org/10.2298/JSC180103052K.
- Hussein, M. S.; Al-Lami, N.; Al-Jeilawi, O. H. R. Design, Synthesis of Imidazolone and Oxazepine Derivatives Bearing Imidazo(2,1-b)Thiazole along with its Antimicrobial Activity. Chem. Methodol. 2022, 6, 319–330.
- Cocco, M. T.; Congiu, C.; Lilliu, V.; Onnis, V. Synthesis and Antiproliferative Activity of 2,6-Dibenzylamino-3,5-Dicyanopyridines on Human Cancer Cell Lines. Eur. J. Med. Chem. 2005, 40, 1365–1372. DOI: https://doi.org/10.1016/j.ejmech.2005.07.005.
- Herlt, A. J.; Rickards, R. W.; Wu, J. P. J. The Structure of Streptonigrone, and a Comment on the Biosynthesis of the Streptonigrin Antibiotics. J. Antibiot. 1985, 38, 516–518. DOI: https://doi.org/10.7164/antibiotics.38.516.
- Wang, H.; Yeo, S. L.; Xu, J.; Xu, X.; He, H.; Ronca, F.; Ting, A. E.; Wang, Y.; Yu, V. C.; Sim, M. M. Isolation of Streptonigrin and Its Novel Derivative from Micromonospora as Inducing Agents of p53-Dependent Cell Apoptosis. J. Nat. Prod. 2002, 65, 721–724. DOI: https://doi.org/10.1021/np0104572.
- Boger, D. L.; Burke, S. D.; Engler, T. A.; Fraser-Reid, B.; Greco, M. N.; Helquist, P.; Jacobi, P. A.; Jung, M. E.; Kozikowski, A. P.; Martin, S. E.; et al. Strategies and Tactics in Organic Synthesis; Lindberg, T., Ed.; Academic Press: San Diego, 1988; Vol. 2, p 1.
- Kim, E. S. Abemaciclib: First Global Approval. Drugs. 2017, 77, 2063–2070. DOI: https://doi.org/10.1007/s40265-017-0840-z.
- Ma, X.; Gang, D. R. The Lycopodium Alkaloids. Nat. Prod. Rep. 2004, 21, 752–772. DOI: https://doi.org/10.1039/b409720n.
- Vidaillac, C.; Guillon, J.; Arpin, C.; Forfar-Bares, I.; Ba, B. B.; Grellet, J.; Moreau, S.; Caignard, D.-H.; Jarry, C.; Quentin, C. Synthesis of Omeprazole Analogues and Evaluation of These as Potential Inhibitors of the Multidrug Efflux Pump NorA of Staphylococcus aureus. Antimicrob. Agents. Chemother. 2007, 51, 831–838. DOI: https://doi.org/10.1128/AAC.01306-05.
- Tew, G. N.; Aamer, K. A.; Shunmugam, R. Incorporation of Terpyridine into the Side Chain of Copolymers to Create Multi-Functional Materials. Polymer 2005, 46, 8440–8447. DOI: https://doi.org/10.1016/j.polymer.2005.04.084.
- Levy, S. B.; Alekshun, M. N.; Podlogar, B. L.; Ohemeng, K.; Verma, A. K.; Warchol, T.; Bhatia, B.; Bowser, T.; Grier, M. U.S. Patent Appl., 2005124678 A1 20050609, 2005.
- May, B. C. H.; Zorn, J. A.; Witkop, J.; Sherrill, J.; Wallace, A. C.; Legname, G.; Prusiner, S. B.; Cohen, F. E. Structure-Activity Relationship Study of Prion Inhibition by 2-Aminopyridine-3,5-Dicarbonitrile-Based Compounds: Parallel Synthesis, Bioactivity, and in Vitro Pharmacokinetics. J. Med. Chem. 2007, 50, 65–73. DOI: https://doi.org/10.1021/jm061045z.
- Chen, H.; Zhang, W.; Tam, R.; Raney, A. K. PCT Int. Appl. WO2005058315 A120050630, 2005.
- Harada, H.; Watanuki, S.; Takuwa, T.; Kawaguchi, K.; Okazaki, T.; Hirano, Y.; Saitoh, C. PCT Int. Appl. WO 2002006237 A1 20020124, 2002.
- Chang, L. C. W.; von Frijtag Drabbe Künzel, J. K.; Mulder-Krieger, T.; Spanjersberg, R. F.; Roerink, S. F.; van den Hout, G.; Beukers, M. W.; Brussee, J.; Ijzerman, A. P. A Series of Ligands Displaying a Remarkable Agonistic-Antagonistic Profile at the Adenosine A1 Receptor. J. Med. Chem. 2005, 48, 2045–2053. DOI: https://doi.org/10.1021/jm049597+.
- Fredholm, B. B.; Ijzerman, A. P.; Jacobson, K. A.; Klotz, K. N. Linden, International Union of Pharmacology. XXV. Nomenclature and Classification of Adenosine Receptors. J. Pharmacol. Rev. 2001, 53, 527–552.
- Reddy, T. R. K.; Mutter, R.; Heal, W.; Guo, K.; Gillet, V. J.; Pratt, S.; Chen, B. Library Design, Synthesis, and Screening: Pyridine Dicarbonitriles as Potential Prion Disease Therapeutics. J. Med. Chem. 2006, 49, 607–615. DOI: https://doi.org/10.1021/jm050610f.
- Perrier, V.; Wallace, A. C.; Kaneko, K.; Safar, J.; Prusiner, S. B.; Cohen, F. E. Mimicking Dominant Negative Inhibition of Prion Replication through Structure-Based Drug Design. Proc. Natl. Acad. Sci. USA 2000, 97, 6073–6078. DOI: https://doi.org/10.1073/pnas.97.11.6073.
- Mamgain, R.; Singh, R.; Rawat, D. S. DBU-Catalyzed Three-Component One-Pot Synthesis of Highly Functionalized Pyridines in Aqueous Ethanol. J. Heterocyclic. Chem. 2009, 46, 69–73. DOI: https://doi.org/10.1002/jhet.32.
- Sobhani, S.; Honarmand, M. Ionic Liquid Immobilized on γ-Fe2O3 Nanoparticles: A New Magnetically Recyclable Heterogeneous Catalyst for One-Pot Three-Component Synthesis of 2-Amino-3,5-Dicarbonitrile-6-Thio-Pyridines. Appl.Catal. A: Gen. 2013, 467, 456–462. DOI: https://doi.org/10.1016/j.apcata.2013.08.006.
- Singh, K. N.; Singh, S. K. Microwave-Assisted, One-Pot Multicomponent Synthesis of Highly Substituted Pyridines Using KF/Alumina. Arkivoc. 2009, 2009, 153–160. DOI: https://doi.org/10.3998/ark.5550190.0010.d13.
- Sobhani, S.; Honarmand, M. 2-Hydroxyethylammonium Acetate: A Reusable Task-Specific Ionic Liquid Promoting One-Pot, Three-Component Synthesis of 2-Amino-3,5-Dicarbonitrile-6-Thio-Pyridines. C. R. Chimie. 2013, 16, 279–286. DOI: https://doi.org/10.1016/j.crci.2012.10.011.
- Kottawar, S. S.; Siddiqui, S. A.; Bhusare, S. R. Scandium Triflate-Catalyzed One-Pot Multi-Component Synthesis of 2-Amino-6- Thiopyridine-3,5-Dicarbonitriles. Heterocycl. Commun. 2012, 18, 249–252.
- Das, B.; Ravikanth, B.; Kumar, A. S.; Kanth, B. S. An Efficient Procedure for the Synthesis of Substituted Pyridines Using KF.Al2O3. J. Heterocyclic. Chem. 2009, 46, 1208–1212. DOI: https://doi.org/10.1002/jhet.206.
- Ranu, B. C.; Jana, R.; Sowmiah, S. An Improved Procedure for the Three-Component Synthesis of Highly Substituted Pyridines Using Ionic Liquid. J. Org. Chem. 2007, 72, 3152–3154. DOI: https://doi.org/10.1021/jo070015g.
- Safaei-Ghomi, J.; Ghasemzadeh, M. A. CuI Nanoparticles: A Highly Active and Easily Recyclable Catalyst for the Synthesis of 2-Amino-3,5-Dicyano-6-Sulfanyl Pyridines. J. Sulfur Chem. 2012, 1, 1–9.
- Kumari, S.; Shekhar, A.; Pathak, D. D. Graphene Oxide–TiO2 Composite: An Efficient Heterogeneous Catalyst for the Green Synthesis of Pyrazoles and Pyridines. New J. Chem. 2016, 40, 5053–5060. DOI: https://doi.org/10.1039/C5NJ03380B.
- Niknam, K.; Hosseini, A. R. Synthesis of 2-Amino-3,5-Dicarbonitrile-6-Thiopyridines Using Silica-Bonded N-Propyldiethylenetriamine as a Heterogeneous Solid Base Catalyst. Org. Chem. Res. 2017, 3, 16–24.
- Khan, M. N.; Pal, S.; Parvin, T.; Choudhury, L. H. A Simple and Efficient Method for the Facile Access of Highly Functionalized Pyridines and Their Fluorescence Property Studies. RSC Adv. 2012, 2, 12305–12314. DOI: https://doi.org/10.1039/c2ra21385k.
- Safaei-Ghomi, J.; Ghasemzadeh, M. A.; Mehrabi, M. Calcium Oxide Nanoparticles Catalyzed One-Step Multicomponent Synthesis of Highly Substituted Pyridines in Aqueous Ethanol Media. Sci. Iran. Tran. C. 2013, 20, 549–554.
- Shinde, P. V.; Sonar, S. S.; Shingate, B. B.; Shingare, M. S. Boric Acid Catalyzed Convenient Synthesis of 2-Amino-3,5-Dicarbonitrile-6-Thio-Pyridines in Aqueous Media. Tetrahedron. Lett. 2010, 51, 1309–1312. DOI: https://doi.org/10.1016/j.tetlet.2009.12.146.
- Gujar, J. B.; Chaudhari, M. A.; Kawade, D. S.; Shingare, M. S. Sodium Chloride: A Proficient Additive for the Synthesis of Pyridine Derivatives in Aqueous Medium. Tetrahedron. Lett. 2014, 55, 6939–6942. DOI: https://doi.org/10.1016/j.tetlet.2014.10.125.
- Banerjee, S.; Sereda, G. One-Step, Three-Component Synthesis of Highly Substituted Pyridines Using Silica Nanoparticle as Reusable Catalyst. Tetrahedron. Lett. 2009, 50, 6959–6962. DOI: https://doi.org/10.1016/j.tetlet.2009.09.137.
- Thimmaiah, M.; Li, P.; Regati, S.; Chen, B.; Zhao Cong-Gui, J. Multi-Component Synthesis of 2-Amino-6-(Alkylthio)Pyridine-3,5-Dicarbonitriles Using Zn(II) and Cd(II) Metal–Organic Frameworks (MOFs) under Solvent-Free Conditions. Tetrahedron. Lett. 2012, 53, 4870–4872. DOI: https://doi.org/10.1016/j.tetlet.2012.06.139.
- Sridhar, M.; Ramanaiah, B. C.; Narsaiah, C.; Mahesh, B.; Kumaraswamy, M.; Mallu, K. K. R.; Ankathi, V. M.; Rao, P. S. Novel ZnCl2-Catalyzed One-Pot Multicomponent Synthesis of 2-Amino-3,5-Dicarbonitrile-6-Thio-Pyridines. Tetrahedron. Lett. 2009, 50, 3897–3900. DOI: https://doi.org/10.1016/j.tetlet.2009.04.051.
- Takale, S.; Patil, J.; Padalkar, V.; Pisal, R.; Chaskar, A. O-Iodoxybenzoic Acid in Water: Optimized Green Alternative for Multicomponent One-Pot Synthesis of 2-Amino-3,5-Dicarbonitrile-6-Thiopyridines. J. Braz. Chem. Soc. 2012, 23, 966–969. DOI: https://doi.org/10.1590/S0103-50532012000500024.
- Banerjee, B. Recent Developments on Organo-Bicyclo-Bases Catalyzed Multi-Component Synthesis of Biologically Relevant Heterocycles. Curr. Org. Chem. 2018, 22, 208–233. DOI: https://doi.org/10.2174/1385272821666170703123129.
- Kaur, G.; Thakur, S.; Kaundal, P.; Chandel, K.; Banerjee, B. p-Dodecylbenzenesulfonic Acid: An Efficient Brønsted Acid-Surfactant-Combined Catalyst to Carry out Diverse Organic Transformations in Aqueous Medium. Chemistry Select. 2018, 3, 12918–12936. DOI: https://doi.org/10.1002/slct.201802824.
- Banerjee, B.; Bhardwaj, V.; Kaur, A.; Kaur, G.; Singh, A. Catalytic Applications of Saccharin and Its Derivatives in Organic Synthesis. Curr. Org. Chem. 2020, 23, 3191–3205. DOI: https://doi.org/10.2174/1385272823666191121144758.
- Basafa, S.; Davoodnia, A.; Beyramabadi, S. A.; Pordel, M. A Probe into Hydrolysis of Nitrile Moiety in 2-Amino-1-Methyl-4-Oxo-1,4-Dihydroquinoline-3-Carbonitrile. Chem. Methodol. 2021, 5, 59–69.
- Selmi, A.; Zarei, A.; Tachoua, W.; Puschmann, H.; Teymourinia, H.; Ramazani, A. Synthesis and Structural Analysis of a Novel Stable Quinoline Dicarbamic Acid: X-Ray Single Crystal Structure of (2-((4-((2- (Carboxy(Methyl)Amino)Ethoxy)Carbonyl) Quinoline-2-yl)Oxy) Ethyl) (Methyl)-Carbamic Acid and Molecular Docking Assessments to Test Its Inhibitory Potential against SARS-CoV-2 Main Protease. Chem. Methodol. 2022, 6, 463–474.
- Brahmachari, G.; Banerjee, B. Sulfamic Acid-Catalyzed Carbon-Carbon and Carbon-Heteroatom Bond Forming Reactions: An Overview. Curr. Organocatalysis. 2016, 3, 93–124. DOI: https://doi.org/10.2174/2213337202666150812230830.
- Brahmachari, G.; Banerjee, B. Facile and Chemically Sustainable One-Pot Synthesis of a Wide Array of Fused O- and N-Heterocycles Catalyzed by Trisodium Citrate Dihydrate under Ambient Conditions. Asian J. Org. Chem. 2016, 5, 271–286. DOI: https://doi.org/10.1002/ajoc.201500465.
- Brahmachari, G.; Nurjamal, K. Trisodium Citrate Dihydrate-Catalyzed One-Pot Three-Component Synthesis of Biologically Relevant Diversely Substituted 2-Amino-3-Cyano-4-(3- Indolyl)-4H-Chromenes under Eco-Friendly Conditions. Curr. Green Chem. 2016, 3, 248–258. DOI: https://doi.org/10.2174/2213346104666170306100839.
- Saltmarsh, M.; Insall, L. Essential Guide to Food Additives, 4th ed.; RSC Publishing, UK, 2013; p. 148.
- Winter, R. A Consumer’s Dictionary of Food Additives, 7th ed.; Three Rivers Press, Crown Publishing Group, New York, 2009, p. 538
- Oçpik, V.; Saaremets, I.; Medijainen, L.; Karelson, K.; Janson, T.; Timpmann, S. Effects of Sodium Citrate Ingestion before Exercise on Endurance Performance in Well Trained College Runners. Br. J. Sports Med. 2003, 37, 485–489.
- Gruber, C. M. Jr; Halbeisen, W. A. A Study on the Comparative Toxic Effects of Citric Acid and its Sodium Salts. J. Pharmacol. Exp. Ther. 1948, 94, 65–67.
- Kaur, G.; Devi, P.; Thakur, S.; Kumar, A.; Chandel, R.; Banerjee, B. One-Pot Pseudo Five Component Synthesis of Biologically Relevant 1,2,6-Triaryl-4-Arylamino-Piperidine-3- Ene-3-Carboxylates: A Decade Update. ChemistrySelect. 2018, 3, 9892–9910. DOI: https://doi.org/10.1002/slct.201801887.
- Brahmachari, G.; Banerjee, B. Functionalized 2-Amino-3-Cyano-4H-Pyrans and Pyran-Annulated Heterocyclic Scaffolds via an Eco-Friendly Multicomponent Reaction at Room Temperature Using Urea as a Novel Organo-Catalyst. ACS Sustainable. Chem. Eng. 2014, 2, 411–422. DOI: https://doi.org/10.1021/sc400312n.
- Brahmachari, G.; Banerjee, B. A Comparison between Catalyst-Free and ZrOCl2.8H2O Catalyzed Strecker Reactions for the Rapid and Solvent-Free One-Pot Synthesis of Racemic α-Aminonitrile Derivatives. Asian J. Org. Chem. 2012, 1, 251–258. DOI: https://doi.org/10.1002/ajoc.201200055.
- Banerjee, B.; Brahmachari, G. Ammonium Chloride Catalysed One-Pot Multicomponent Synthesis of 1,8-Dioxo-Octahydroxanthenes and N-Aryl-1,8-Dioxodecahydroacridines under Solvent Free Conditions. J. Chem. Res. 2014, 38, 745–750. DOI: https://doi.org/10.3184/174751914X14177132210020.
- Brahmachari, G.; Laskar, S.; Banerjee, B. Eco-Friendly, One-Pot Multicomponent Synthesis of Pyran Annulated Heterocyclic Scaffolds at Room Temperature Using Ammonium or Sodium Formate as Non-Toxic Catalyst. J. Heterocycl. Chem. 2014, 51, 303–308.
- Kaur, G.; Shamim, M.; Bhardwaj, V.; Gupta, V. K.; Banerjee, B. Mandelic Acid Catalyzed One-Pot Three-Component Synthesis of α-Aminonitriles and α-Aminophosphonates under Solvent-Free Conditions at Room Temperature. Synth. Commun. 2020, 50, 1545–1560. DOI: https://doi.org/10.1080/00397911.2020.1745844.
- Taherkhani, H.; Ramazani, A.; Sajjadifar, S.; Aghahossieini, H.; Rezaei, A. Design and Preparation of Copper(II)–Mesalamine Complex Functionalized on Silica-Coated Magnetite Nanoparticles and Study of Its Catalytic Properties for Green and Multicomponent Synthesis of Highly Substituted 4H-Chromenes and PyridinesACS. Omega. 2022, 7, 14972–25622. DOI: https://doi.org/10.1021/acsomega.2c00731.
- Rezayati, S.; Kalantari, F.; Ramazani, A.; Sajjadifar, S.; Aghahosseini, H.; Rezaei, A. Magnetic Silica-Coated Picolylamine Copper Complex [Fe3O4@SiO2@GP/Picolylamine-Cu(II)]-Catalyzed Biginelli Annulation Reaction. Inorg. Chem. 2022, 61, 992–1010. DOI: https://doi.org/10.1021/acs.inorgchem.1c03042.
- Baghernejad, B.; Harzevili, M. R. Nano-Cerium Oxide/Aluminum Oxide: An Efficient and Useful Catalyst for the Synthesis of Tetrahydro[a]Xanthenes-11-One Derivatives. Chem. Methodol. 2021, 5, 90–95.
- Irannejad-Gheshlaghchaei, N.; Zare, A.; Banaei, A.; Kaveh, H.; Varavi, N. N,N,N',N'-Tetramethyl-N,N'-Bis(Sulfo)Ethane-1,2- Diaminium Mesylate as a Highly Effective and Dualfunctional Catalyst for the Synthesis of 1- Thioamidoalkyl-2-Naphthols. Chem. Methodol. 2020, 4, 400–407. DOI: https://doi.org/10.33945/SAMI/CHEMM.2020.4.3.
- Kaur, G.; Singh, A.; Bala, K.; Devi, M.; Kumari, A.; Devi, S.; Devi, R.; Gupta, V. K.; Banerjee, B. Naturally Occurring Organic Acid-Catalyzed Facile Diastereoselective Synthesis of Biologically Active (E)-3-(Arylimino)Indolin-2-One Derivatives in Water at Room Temperature. Curr. Org. Chem. 2019, 23, 1778–1788. DOI: https://doi.org/10.2174/1385272822666190924182538.
- Banerjee, B.; Priya, A.; Sharma, A.; Kaur, G.; Kaur, M. Sulfonated β-Cyclodextrins: Efficient Supramolecular Organocatalysts for Diverse Organic Transformations. Phys. Sci. Rev 2022, 7, 539–565. DOI: https://doi.org/10.1515/psr-2021-0080.
- Banerjee, B.; Singh, A.; Kaur, G. Baker’s Yeast (Saccharomyces Cerevisiae) Catalyzed Synthesis of Bioactive Heterocycles and Some Stereoselective Reactions. Phys. Sci. Rev. 2022, 7, 301–323. DOI: https://doi.org/10.1515/psr-2021-0021.
- Kaur, G.; Bala, K.; Devi, S.; Banerjee, B. Camphorsulfonic Acid (CSA): An Efficient Organocatalyst for the Synthesis or Derivatization of Heterocycles with Biologically Promising Activities. Curr. Green Chem. 2018, 5, 150–167. DOI: https://doi.org/10.2174/2213346105666181001113413.
- Singh, A.; Kaur, G.; Kaur, A.; Gupta, V. K.; Banerjee, B. A General Method for the Synthesis of 3,3-Bis(Indol-3-Yl)Indolin-2-Ones, Bis(Indol-3-Yl)(Aryl)Methanes and Tris(Indol-3-yl)Methanes Using Naturally Occurring Mandelic Acid as an Efficient Organo-Catalyst in Aqueous Ethanol at Room Temperature. Curr. Green Chem. 2020, 7, 128–140. DOI: https://doi.org/10.2174/2213346107666200228125715.
- Banerjee, B.; Kaur, G.; Kaur, N. p-Sulfonic Acid Calix[n]Arene Catalyzed Synthesis of Bioactive Heterocycles: A Review. Curr. Org. Chem. 2021, 25, 209–222. DOI: https://doi.org/10.2174/1385272824999201019162655.
- Kaur, G.; Kumar, R.; Saroch, S.; Gupta, V. K.; Banerjee, B. Mandelic Acid: An Efficient Organo-Catalyst for the Synthesis of 3-Substituted-3hydroxy-Indolin-2-Ones and Related Derivatives in Aqueous Ethanol at Room Temperature. Curr. Organocatal. 2021, 8, 147–159. DOI: https://doi.org/10.2174/2213337207999200713145440.
- Banik, B. K.; Banerjee, B.; Kaur, G.; Saroch, S.; Kumar, R. Tetrabutylammonium Bromide (TBAB) Catalyzed Synthesis of Bioactive Heterocycles. Molecules. 2020, 25, 5918. DOI: https://doi.org/10.3390/molecules25245918.
- Kaur, G.; Singh, D.; Singh, A.; Banerjee, B. Camphor Sulfonic Acid Catalyzed Facile and General Method for the Synthesis of 3,3′-(Arylmethylene)Bis(4-Hydroxy-2H-Chromen-2-Ones), 3,3′-(Arylmethylene)Bis(2-Hydroxynaphthalene-1,4-Diones) and 3,3′-(2-Oxoindoline-3,3-Diyl)Bis(2-Hydroxynaphthalene-1,4-Dione) Derivatives at Room Temperature. Synth. Commun. 2021, 51, 1045–1057. DOI: https://doi.org/10.1080/00397911.2020.1856877.
- Kaur, G.; Moudgil, R.; Shamim, M.; Gupta, V. K.; Banerjee, B. Camphor Sulfonic Acid Catalyzed a Simple, Facile, and General Method for the Synthesis of 2-Arylbenzothiazoles, 2-Arylbenzimidazoles, and 3H-Spiro[Benzo[d]Thiazole-2,3′-Indolin]-2′-Ones at Room Temperature. Synth. Commun 2021, 51, 1100–1120. DOI: https://doi.org/10.1080/00397911.2020.1870043.
- Kaur, G.; Singh, A.; Kaur, N.; Banerjee, B. A General Method for the Synthesis of Structurally Diverse Quinoxalines and Pyrido-Pyrazine Derivatives Using Camphor Sulfonic Acid as an Efficient Organo-Catalyst at Room Temperature. Synth. Commun 2021, 51, 1121–1131. DOI: https://doi.org/10.1080/00397911.2021.1873383.
- Kaur, M.; Priya, A.; Sharma, A.; Singh, A.; Banerjee, B. Glycine and Its Derivatives Catalyzed One-Pot Multicomponent Synthesis of Bioactive Heterocycles. Synth. Commun. 2022, . in press. DOI: https://doi.org/10.1080/00397911.2022.2090262.