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S.  Hotha, Anegundi, R. I., and Natu, A. A., ?Expedient synthesis of 1,2,3-triazole-fused tetracyclic compounds by intramolecular Huisgen ('click') reactions on carbohydrate-derived azido-alkynes?, Tetrahedron Letters, vol. 46, no. 27, pp. 4585-4588, 2005.\par \par P. M.  Chincholkar, Puranik, V. G., and Deshmukh, A. Rakeeb A., ?Efficient synthesis of azetidine-2,3-diones from L-(+)-diethyl tartrate?, Synlett, no. 14, pp. 2242-2246, 2007.\par \par A. P.  Amrute, Sahoo, S., Bordoloi, A., Hwang, Y. Kyu, Hwang, J. - S., and Halligudi, S. B., ?MoO3/SiO2: an efficient and selective catalyst for the synthesis 1,3-dioxolane and 1,3-dioxane?, Catalysis Communications, vol. 10, no. 10, pp. 1404-1409, 2009.\par \par S. G.  Agalave, Maujan, S. R., and Pore, V. S., ?Click chemistry: 1,2,3-triazoles as pharmacophores?, Chemistry-an Asian Journal, vol. 6, no. 10, pp. 2696-2718, 2011.\par \par G.  Pandey, Gupta, N. R., and Gadre, S. R., ?Construction of the 5,10b-phenanthridine skeleton using [3+2]-cycloaddition of a non-stabilized azomethine ylide: total synthesis of (+/-)-maritidine and (+/-)-crinine alkaloids?, European Journal of Organic Chemistry, no. 4, pp. 740-750, 2011.\par \par A. S.  Nagare and Kumar, A., ?Eutectic mixture-directed kinetics of Diels-Alder reaction?, Indian Journal of Chemistry Section A-Inorganic Bio-Inorganic Physical Theoretical & Analytical Chemistry, vol. 50, no. 6, pp. 788-792, 2011.\par \par G.  Pandey, Kumar, R., Banerjee, P., and Puranik, V. G., ?One-step stereospecific strategy for the construction of the core structure of the 5,11-methanomorphanthridine alkaloids in racemic as well as in optically pure form: synthesis of (+/-)-pancracine and (+/-)-brunsvigine?, European Journal of Organic Chemistry, no. 24, pp. 4571-4587, 2011.\par \par S. G.  Agalave, Pharande, S. G., Gade, S. M., and Pore, V. S., ?Alumina-supported copper iodide: an efficient and recyclable catalyst for microwave-assisted synthesis of 1,4-disubstituted 1,2,3-triazoles via three-component reaction in water?, Asian Journal of Organic Chemistry, vol. 4, no. 9, pp. 943-951, 2015.\par \par V. S.  Pore, Divse, J. M., Charolkar, C. R., Nawale, L. U., Khedkar, V. M., and Sarkar, D., ?Design and synthesis of 11 alpha-substituted bile acid derivatives as potential anti-tuberculosis agents?, Bioorganic & Medicinal Chemistry Letters, vol. 25, no. 19, pp. 4185-4190, 2015.\par \par A.  Pathak and Singh, A. P., ?Synthesis and characterization of D-2PA-Pd(II)@SBA-15 catalyst via ``click chemistry'': highly active catalyst for Suzuki coupling reactions?, Journal of Porous Materials, vol. 24, no. 2, pp. 327-340, 2017.\par \par R. A.  Dhokale and Mhaske, S. B., ?Transition-metal-catalyzed reactions involving arynes?, Synthesis-Stuttgart, vol. 50, no. 1, pp. 1-16, 2018.\par \par B. Sai Allaka, Basavoju, S., and Krishna, G. Rama, ?Photoinduced multicomponent regioselective synthesis of 1,4,5-trisubstituted-1,2,3-triazoles: transition metal-, azide- and oxidant-free protocol?, Advanced Synthesis & Catalysis, vol. 363, no. 14, pp. 3560-3565, 2021.\par \par N. K.  Verma, Bera, S., Gonnade, R., and Mondal, D., ?Regioselective synthesis of 1,4,5-trisubstituted 1,2,3-triazole derivatives from alpha,beta-unsaturated carbonyls?, European Journal of Organic Chemistry, vol. 2022, no. 28, p. e202200317, 2022.\par \par B. Sai Allaka, Basavoju, S., and Gamidi, R. Krishna, ?Transition metal- and oxidant-free regioselective synthesis of 3,4,5-trisubstituted pyrazoles by means of [3+2] cycloaddition reactions?, ChemistrySelect, vol. 7, no. 11, p. e202200605, 2022.\par \par S. A.  Galave, Kadam, K. S., Sonawane, A. D., Pansare, V. R., and Garud, D. R., ?Metal-free isoamyl nitrite mediated efficient synthesis of 1,2,4-oxadiazoles?, Tetrahedron Letters, vol. 125, p. 154616, 2023.\par \par M.  Kanchrana, Krishna, G. Rama, Dey, B., Pandey, N., Guru, S. Kumar, Sangolkar, A. Ashok, Pawar, R., and Basavoju, S., ?Ionic liquid assisted green synthesis of quinoxaline based bisspirooxindoles: anticancer evaluation and molecular dynamics?, CHEMISTRYSELECT, vol. 9, p. e202403608, 2024.\par \par }