[4]
Claramunt RM, Elguero J. Active Pharmaceutical IngredientsApplications of NMR Spectroscopy in the Solid State. Madrid: CSIC 2019.
[5]
Larina LI. Tautomerism and structure of azoles. Advances in Heterocyclic Chemistry. Elsevier Ltd 2018; 233-321.
[6]
Elguero J, Marzin C, Katritzky AR, Linda P. The Tautomerism of heterocycles. New York: Academic Press 1976.
[8]
Minkin VI, Garnovskii AD, Elguero J, Katritzky AR, Denisko OV. The tautomerism of heterocycles: Five-membered rings with two or more heteroatomsadvances in heterocyclic chemistry. New York 2000; 157-323.
[9]
Taylor PJ, van der Zwan G, Antonov L. Tautomerism: Introduction, history, and recent developments in experimental and theoretical methods. Antonov L, editor Tautomerism. Weinheim, Germany: Wiley-VCH Verlag GmbH Co. KGaA 2013.
[10]
Sanchez-Muñoz L, Garrido Fernandez L, Muñoz Fraile F, Sanz Lazaro J. Applications of NMR Spectroscopy in the Solid State. Madrid: CSIC 2019.
[25]
Frisch MJ, Trucks GW, Schlegel HB, et al. Gaussian 09. Wallingford, CT: Gaussian, Inc. 2009.
[34]
Zala. Synthesis and biological evaluation of 2,4,5-triphenyl-1H-imidazole-1-yl Derivatives. J Appl Pharm Sci 2012; 2: 202-8.
[35]
Maity S, Ahmad S, Singh S, Baranwal G. Imidazole- A new profile of various pharmacological activities. Eur J Pharm Med Res 2017; 4: 322-4.
[44]
Coispeau G, Elguero J. Reaction des hydrazines avec les composés difonctionnels-1,3 Synthèse de dérivés du pyrazole. Bull Soc Chem Fr 1970; 2717-36.
[45]
Elguero J, Silva A, Tomé A. Five-membered heterocycles: 1,2-azolespart 1 pyrazoles in: Alvarez-Builla J, Vaquero Jj, Barluenga J, Editors Modern Heterocyclic Chemistry. Weinheim, Germany: Wiley-VCH Verlag GmbH Co. KGaA 2011.
[50]
Elguero J, Goya P, Jagerovic N, Silva AMS. Pyrazoles as drugs: Facts and fantasies. Targets Heterocycl Syst 2002; 6: 52-98.
[64]
Higdon J, Drake VJ. Curcumin An evidence-based approach to phytochemicals and other dietary factors. New York: Thieme Medical Publishers 2012.
[73]
Yet L. Five-membered ring systems: with more than one n atom.progress in heterocyclic chemistry. Elsevier 2012; 243-79.
[79]
Santhi N, Prabhakaran B. Synthesis, spectroscopic characterizations and quantum chemical computational studies of 6-fluoro-N-(4-substitutedbenzylidene)-1H-indazol-3- amine. Der Pharma Chem 2016; 8: 44-55.
[82]
Shalini K, Sharma P, Kumar N. Imidazole and its biological activities: A review. Chem Sin 2010; 1: 36-47.
[84]
Verma A, Joshi S, Singh D. Imidazole: Having versatile biological activities. J Chem 2013; 2013: 1-12.
[94]
Vargas JAR, Lopez AG, Piñol MC, Froeyen M. Molecular docking study on the interaction between 2-substituted-4,5-difuryl Imidazoles with different protein target for antileishmanial activity. J Appl Pharm Sci 2018; 8: 14-22.
[97]
Singh VK, Parle Am. The intriguing benzimidazole: A review. Int J Pharm Sci Res 2019; 10: 1540-52.
[102]
Anand K, Wakode S. Development of drugs based on Benzimidazole Heterocycle: Recent advancement and insights. Int J Chem Stud 2017; 5: 350-62.
[129]
Singh VK, Rishishwar P, Bhardwaj P, Alok S. Benzotriazole: A heterocyclic molecule with diversified pharmacological activities. Int J Pharm Sci Res 2017; 8: 446-56.
[130]
Dennis Hall C, Panda SS. The benzotriazole storyadvances in heterocyclic chemistry. Elsevier Ltd 2016; 119: 1-23.
[144]
Namratha B, Gaonkar SL. Innovare academic sciences 1,2,4-triazoles : synthetic strategies and pharamacological profiles. Int J Pharm Pharm Sci 2014; 6: 73-80.
[145]
Martin A, Martin R. A review on the Antimicrobial, Analgesic and Anti-inflamamatory activity of 1,2,4-triazoles. Indian Res J Pharm Sci 2014; 2: 106-6.
[150]
Bhatt U. Five-membered heterocycles with four heteroatoms: tetrazoles modern heterocyclic chemistry. Weinheim, Germany: Wiley- VCH Verlag GmbH Co. KGaA 2011; 1401-30.
[156]
Sanz D, Claramunt RM, Roussel C, Alkorta I, Elguero J. The structure of N-benzylazoles from pyrrole to carbazole: geometries and energies. Indian J Heterocycl Chem 2018; 28: 1-10.