Recent advances on the transition-metal-catalyzed synthesis of imidazopyridines: an updated coverage

Scholarly Works

• Gadekar, A. B.; Sonam; Shinde, V. N.; Bhawani; Rangan, K.; Kumar, A. Visible Light‐Driven Difluoroalkoxylation of Imidazopyridines Using N‐Fluorobenzenesulfonimide as Fluorinating Agent. Advanced Synthesis & Catalysis 2024. doi:10.1002/adsc.202400755
• Maikhuri, V. K.; Mathur, D.; Chaudhary, A.; Kumar, R.; Parmar, V. S.; Singh, B. K. Transition-Metal Catalyzed Synthesis of Pyrimidines: Recent Advances, Mechanism, Scope and Future Perspectives. Topics in current chemistry (Cham) 2024, 382, 4. doi:10.1007/s41061-024-00451-2
• Narayan, A.; Patel, S.; Baile, S. B.; Jain, S.; Sharma, S. Imidazo[1,2-A]Pyridine: Potent Biological Activity, SAR and Docking Investigations (2017-2022). Infectious disorders drug targets 2024, 24, e200324228067. doi:10.2174/0118715265274067240223040333
• Kaur, P.; Gurjar, K. K.; Arora, T.; Bharti, D.; Kaur, M.; Kumar, V.; Parkash, J.; Kumar, R. Efficient synthesis and mechanistic insights for the formation of imidazo[1,2-a]pyridines via multicomponent decarboxylative coupling using chitosan-supported copper catalysts. Molecular Catalysis 2023, 550, 113582. doi:10.1016/j.mcat.2023.113582
• Liu, X.; Guo, X.; Jiang, Z.; Li, C.; Nan, Z.; Liu, Y. Photocatalyzed intermolecular C–N bond formation for the synthesis of imidazo[1,2-a]pyridines. Tetrahedron Letters 2023, 129, 154746. doi:10.1016/j.tetlet.2023.154746
• Meena, N.; Shinde, V. N.; Sonam; Swami, P. N.; Rangan, K.; Kumar, A. Catalyst-Controlled Regiodivergent Oxidative Annulation of 2-Arylimidazo[1,2-a]pyridines with Cinnamaldehyde Derivatives for Construction of Fused N-Heterocyclic Frameworks. The Journal of organic chemistry 2023, 88, 12902–12913. doi:10.1021/acs.joc.3c00717
• Nikoshvili, L. Z.; Matveeva, V. G. Recent Progress in Pd-Catalyzed Tandem Processes. Catalysts 2023, 13, 1213. doi:10.3390/catal13081213
• Vchislo, N. V.; Fedoseeva, V. G.; Verochkina, E. A. The Reactions of p-Tosylmethyl Isocyanide with Aldehydes in the Synthesis of Heterocyclic Compounds: A Review. Mini-Reviews in Organic Chemistry 2023, 20, 372–393. doi:10.2174/1570193x19999220523113243
• Sakhuja, R.; Kumar, A. doi:10.1002/9781119774167.ch11
• Seth, K.; Sunny, S.; Maingle, M.; Sheeba, L.; Pathan, F. R.; J., G. S.; Juloori, H.; Gadewar, S. G. Pd-Nanoparticles-Catalyzed C(sp2)–H Arylation for the Synthesis of Functionalized Heterocycles: Recent Progress and Prospects. Synthesis 2023, 56, 611–638. doi:10.1055/a-2060-3488
• Zhong, W.; Zhao, C.; Huang, Q.; Wu, L.; Shi, J.; Li, J.; Lu, W.; Tang, F.; Zhu, L. I2/DTBP Promoted Synthesis of C3-Carbonylated Imidazopyridines from Chromones and 2-Aminopyridines via (3+2) Cycloaddition. Synthesis 2023, 55, 2570–2580. doi:10.1055/a-2058-0119
• Semenova, N. V.; Schmidt, E. Y.; Ushakov, I. A.; Trofimov, B. A. Acetylene-driven multi-molecular assemblies of high complexity: imidazo[1,2-a]pyridines and 5-chloro-N-[2-(imidazo[1,2-a]pyridin-6-yl)vinyl]pyridin-2-amine. Mendeleev Communications 2023, 33, 164–166. doi:10.1016/j.mencom.2023.02.005
• Kumar, R.; Kaur, P.; Gurjar, K.; Arora, T.; Bharti, D.; Dhull, M.; Kumar, V.; Parkash, J. Efficient Synthesis and Mechanistic Insights for the Formation Of Imidazo[1,2-A]Pyridines Via Multicomponent Decarboxylative Coupling Using Chitosan-Supported Copper Catalysts. Elsevier BV 2023. doi:10.2139/ssrn.4519904
• Morja, M. I.; Moradiya, R. B.; Chikhalia, K. H. First-row transition metal for isocyanide-involving multicomponent reactions (IMCR). Molecular diversity 2022, 27, 2895–2934. doi:10.1007/s11030-022-10583-6
• Dai, P.; Xu, H. Novel Chlorination of Imidazo‐Fused Heterocycles via Dichloro(aryl)‐λ3‐iodanes. European Journal of Organic Chemistry 2022, 2022. doi:10.1002/ejoc.202200779
• Mishra, N. P.; Mohapatra, S.; Das, T.; Nayak, S. Imidazo[1,2‐a]pyridine as a promising scaffold for the development of antibacterial agents. Journal of Heterocyclic Chemistry 2022, 59, 2051–2075. doi:10.1002/jhet.4534
• Sharma, R. P.; Mahajan, S.; Slathia, N.; Kapoor, K. K. FeCl3 as an efficient catalyst for the synthesis of styrylquinoxalin-2(1H)-ones. Synthetic Communications 2022, 52, 1069–1078. doi:10.1080/00397911.2022.2070435
• Banerjee, M.; Panjikar, P. C.; Das, D.; Iyer, S.; Bhosle, A. A.; Chatterjee, A. Grindstone chemistry: A "green" approach for the synthesis and derivatization of heterocycles. Tetrahedron 2022, 112, 132753. doi:10.1016/j.tet.2022.132753
• Das, D.; Jena, A. K.; Pal, C. K.; Bourda, L.; Van Hecke, K. CuI Nanoparticle‐Catalyzed Regioselective Synthesis of 3‐Nitro‐2‐arylimidazo[1,2‐a]pyridines using Oxygen as Oxidant. Asian Journal of Organic Chemistry 2022, 11. doi:10.1002/ajoc.202100776
• Panda, J.; Raiguru, B. P.; Mishra, M.; Mohapatra, S.; Nayak, S. Recent Advances in the Synthesis of Imidazo[1,2‐a]pyridines: A Brief Review. ChemistrySelect 2022, 7. doi:10.1002/slct.202103987

Explore citations to this article at