New Methods for Synthesis of 1,2,3-Triazoles: A Review

Author:

Nemallapudi Bakthavatchala Reddy1,Guda Dinneswara Reddy2,Ummadi Nagarjuna3,Avula Balakrishna4,Zyryanov Grigory V.15,Reddy Cirandur Suresh3ORCID,Gundala Sravya1

Affiliation:

1. Department of Chemistry, Chemical Engineering Institute, Ural Federal University, Yekaterinburg, Russia

2. Department of Chemistry, Sogang University, Seoul, South Korea

3. Department of Chemistry, Sri Venkateswara University, Tirupati, Andhra Pradesh, India

4. Department of Chemistry, Rajeev Gandhi Memorial College of Engineering and Technology (Autonomous), Nandyal, Andhra Pradesh, India

5. Department of Chemistry, I. Ya. Postovsky Institute of Organic Synthesis, Ural Division of Russian Academy of Sciences, Yekaterinburg, Russian Federation

Funder

Russian Science Foundation

Publisher

Informa UK Limited

Subject

Materials Chemistry,Organic Chemistry,Polymers and Plastics

Reference44 articles.

1. Efficient synthesis of 5-fluoroalkylated 1H-1,2,3-triazoles and application of the bromodifluoromethylated triazole to the synthesis of novel bicyclic gem-difluorinated 1H-pyrano[3,4-d][1,2,3]-triazol-4-one compounds

2. (a) A. Rani, G. Singh, A. Singh, U. Maqbool, G. Kaur, and J. Singh, “CuAAC-Ensembled 1, 2, 3-Triazole-Linked Isosteres as Pharmacophores in Drug Discovery,” RSC Advances 10, (2010): 5610–35. (b)

3. T. Ince, R. Serttas, B. Demir, H. Atabey, N. Seferoglu, S. Erdogan, E. Sahin, S. Erat, and Y. Nural, “Polysubstituted Pyrrolidine Linked to 1,2,3-Triazoles: Synthesis, Crystal Structure, DFT Studies, Acid Dissociation Constant, Drug-Likeness, and Anti-Proliferative Activity,” Journal of Molecular Structure 1217, (2020): 128400. (c)X. Jiang, X. Hao, L. Jing, G. Wu, D. Kang, X. Liu, and P. Zhan, Recent Applications of Click Chemistry in Drug Discovery, Expert Opinion on Drug Discovery 14, (2019): 779–89. (d)N. Singh, S. K. Pandey, and R. P. Tripathi, “Regioselective [3 + 2] Cycloaddition of Chalcones with a Sugar Azide: Easy Access to 1-(5-Deoxy-d-xylofuranos-5-yl)-4,5-disubstituted-1H-1,2,3-triazoles,” Carbohydrate Research 345, (2010): 1641–48.

4. (a) J. Dinges and C. Lamberth, Bioactive Heterocyclic Compounds Classes: Pharmaceuticals Weinheim (Germany: Wiley-VCH, 2012). (b)

5. G. Knauf-Beiter, C. Fleischhacker, L. Mittermeier, and R. Ligouri, Brighton Crop Protection Conference Pests and Diseases, vol. 2. (1992), 651–56. (c)J. A. Builla, J. J. Vaquero, and J. Barluenga, Modern Heterocyclic Chemistry (Weinheim, Germany: Wiley-VCH, 2011). (d)P. M. Habib, B. R. Raju, V. Kavala, C. Kuo, and C. Yao, Catalyst-Free 1,3-Dipolar Cycloaddition of 3-Nitrochromen with Sodium Azide: A Facile Method for the Synthesis of 4-Aryl-1,4-dihydrochromeno[4,3-d][1,2,3]triazole Derivatives,” Tetrahedron 65, (2009): 5799–04.

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