1. Dharatiben Lakhani, Sheeba Sadiq, Harini Subbaiahgari, Violet Swanson, Jacob Munyon, Sher B. Poudel, Karelle S. Aiken, Shainaz M. Landge, Debosreeta Bose, Debanjana Ghosh, “Structure–Property Correlations in Disubstituted 1,2,3-Triazoles: DFT Insights and Photophysical Analysis”, ACS Omega, 2025  crossref
  2. Sofya P. Balabanova, Alexey A. Voronin, Aleksandr M. Churakov, Michael S. Klenov, Vladimir A. Tartakovsky, “Synthetic Strategies for C‐Amino 1,2,3‐Triazoles and Their Oxides: A Review”, Journal of Heterocyclic Chem, 61:12 (2024), 2106  crossref
  3. G. V. Tsaplin, S. V. Popkov, “Intramolecular ANRORC Reactions in the Series of Diazoles with Three Heteroatoms”, Russ J Org Chem, 58:1 (2022), 1  crossref
  4. Ziqi Su, Hongxin Chai, Juan Xu, Jiarong Li, “ZnCl2-promoted domino reaction of 2-hydroxybenzonitriles with ketones for synthesis of 1,3-benzoxazin-4-ones”, RSC Adv., 11:48 (2021), 29906  crossref
  5. Vitor F. Ferreira, Thais de B. da Silva, Fernanda P. Pauli, Patricia G. Ferreira, Luana da S. M. Forezi, Carolina G. de S. Lima, Fernando de C. da Silva, “Dimroth´s Rearrangement as a Synthetic Strategy Towards New Heterocyclic Compounds”, COC, 24:17 (2020), 1999  crossref
  6. Moulay H. Youssoufi, Pramod K. Sahu, Praveen K. Sahu, Dau D. Agarwal, Mushtaq Ahmad, Mouslim Messali, Siham Lahsasni, Taibi Ben Hadda, “POM analyses of antimicrobial activity of 4H-pyrimido[2,1-b]benzothiazole, pyrazole, and benzylidene derivatives of curcumin”, Med Chem Res, 24:6 (2015), 2381  crossref
  7. L. L. Fershtat, S. S. Ashirbaev, A. S. Kulikov, V. V. Kachala, N. N. Makhova, “Ionic liquid-mediated synthesis of (1H-1,2,3-triazol-1-yl)furoxans by [3 + 2] cycloaddition of azidofuroxans to acetylenes”, Mendeleev Commun., 25:4 (2015), 257–259  mathnet  crossref
  8. Chengming Bian, Kai Wang, Lixuan Liang, Man Zhang, Chuan Li, Zhiming Zhou, “Nitrogen‐Rich Energetic Salts of Bis‐Heterocycle‐Substituted 1,2,3‐Triazole (HTANFT)”, Eur J Inorg Chem, 2014:35 (2014), 6022  crossref
  9. L. V. Batog, V. Yu. Rozhkov, M. I. Struchkova, A. S. Kulikov, N. N. Makhova, “Synthesis of N,N′-bis[4-(1H-1,2,3-triazol-1-yl)furazan-3-yl]-methylenediamine derivatives”, Russ Chem Bull, 62:6 (2013), 1391  crossref
  10. L. V. Batog, L. S. Konstantinova, A. S. Kulikov, N. N. Makhova, “Synthesis of 4,4′-bis(dichloroamino)- and 4,4′-bis(chloroamino)-3,3′-azofurazans, the first representatives of dichloroamino- and chloroaminofurazans”, Russ Chem Bull, 62:6 (2013), 1388  crossref
  11. A. S. Kulikov, M. A. Epishina, L. V. Batog, V. Yu. Rozhkov, N. N. Makhova, L. D. Konyushkin, M. N. Semenova, V. V. Semenov, “Synthesis and antineoplastic properties of (1H-1,2,3-triazol-1-yl)furazans”, Russ Chem Bull, 62:3 (2013), 836  crossref
  12. Liupan Yang, Jiarong Li, Hongxin Chai, Hongyan Lu, Qi Zhang, Daxin Shi, “A Divergent Synthesis of 1,8‐Naphthyridines and Hydropyridopyrimidinones by the Reactions of o‐Aminonitriles with Ketones”, Chin. J. Chem., 31:4 (2013), 443  crossref
  13. Liupan Yang, Daxin Shi, Shu Chen, Hongxin Chai, Danfei Huang, Qi Zhang, Jiarong Li, “Microwave-assisted synthesis of 2,3-dihydropyrido[2,3-d]pyrimidin-4(1H)-ones catalyzed by DBU in aqueous medium”, Green Chem., 14:4 (2012), 945  crossref
  14. Name Reactions in Heterocyclic Chemistry II, 2011, 515  crossref
  15. V. Yu. Rozhkov, L. V. Batog, M. I. Struchkova, “Synthesis of 3-nitramino-4-(1H-1,2,3-triazol-1-yl)-1,2,5-oxadiazoles and their salts”, Russ Chem Bull, 60:8 (2011), 1712  crossref
  16. Catherine J. Smith, Nikzad Nikbin, Steven V. Ley, Heiko Lange, Ian R. Baxendale, “A fully automated, multistep flow synthesis of 5-amino-4-cyano-1,2,3-triazoles”, Org. Biomol. Chem., 9:6 (2011), 1938  crossref
  17. El Sayed H. El Ashry, Said Nadeem, Muhammad Raza Shah, Yeldez El Kilany, Advances in Heterocyclic Chemistry, 101, Advances in Heterocyclic Chemistry Volume 101, 2010, 161  crossref
  18. Comprehensive Organic Name Reactions and Reagents, 2010, 905  crossref
  19. Jian-Hong Tang, Da-Xin Shi, Li-Jun Zhang, Qi Zhang, Jia-Rong Li, “Facile and One-Pot Synthesis of 1,2-Dihydroquinazolin-4(3H)-ones via Tandem Intramolecular Pinner/Dimroth Rearrangement”, Synthetic Communications, 40:5 (2010), 632  crossref
  20. Li-Jun Zhang, Da-Xin Shi, Jia-Rong Li, “Simultaneous Synthesis of Pyrazolopyridines and Pyrazolopyrimidinones Under Microwave Irradiation”, Synthetic Communications, 39:22 (2009), 4010  crossref
1
2
Next