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T
A. B. Danne, Choudhari, A. S., Chakraborty, S., Sarkar, D., Khedkar, V. M., and Shingate, B. B., “Triazole-diindolylmethane conjugates as new antitubercular agents: synthesis, bioevaluation, and molecular docking”, MedChemComm, vol. 9, no. 7, pp. 1114-1130, 2018.
M. H. Shaikh, Subhedar, D. D., Akolkar, S. V., Nagargoje, A. A., Khedkar, V. M., Sarkar, D., and Shingate, B. B., “Tetrazoloquinoline-1,2,3-triazole derivatives as antimicrobial agents: synthesis, biological evaluation and molecular docking study”, Polycyclic Aromatic Compounds, vol. 42, no. 4, pp. 1920-1941, 2022.
S
M. H. Shaikh, Subhedar, D. D., Khan, F. A. Kalam, Sangshetti, J. N., Nawale, L., Arkile, M. A., Sarkar, D., and Shingate, B. B., “Synthesis of novel triazole-incorporated isatin derivatives as antifungal, antitubercular, and antioxidant agents and molecular docking study”, Journal of Heterocyclic Chemistry, vol. 54, no. 413, 2017.
M. H. Shaikh, Subhedar, D. D., Shingate, B. B., Khan, F. A. Kalam, Sangshetti, J. N., Khedkar, V. M., Nawale, L., Sarkar, D., Navale, G. R., and Shinde, S. S., “Synthesis, biological evaluation and molecular docking of novel coumarin incorporated triazoles as antitubercular, antioxidant and antimicrobial agents”, Medicinal Chemistry Research, vol. 25, no. 4, pp. 790-804, 2016.
A. B. Danne, “Synthesis and biological evaluation of novel triazole-biscoumarin conjugates as potential antitubercular and anti-oxidant agents”, Research on Chemical Intermediates, vol. 44, no. 10, pp. 1-28, 2018.
A. H. Kategaonkar, Shinde, P. V., Kategaonkar, A. H., Pasale, S. K., Shingate, B. B., and Shingare, M. S., “Synthesis and biological evaluation of new 2-chloro-3-((4-phenyl-1H-1,2,3-triazol-1-yl)methyl)quinoline derivatives via click chemistry approach”, European Journal of Medicinal Chemistry, vol. 45, no. 7, pp. 3142-3146, 2010.
M. H. Shaikh, Subhedar, D. D., Arkile, M. A., Khedkar, V. M., Jadhav, N. J., Sarkar, D., and Shingate, B. B., “Synthesis and bioactivity of novel triazole incorporated benzothiazinone derivatives as antitubercular and antioxidant agent”, Bioorganic & Medicinal Chemistry Letters, vol. 26, no. 2, pp. 561-569, 2016.
B. B. Shingate, Hazra, B. G., Salunke, D. B., Pore, V. S., Shirazi, F., and Deshpande, M. V., “Synthesis and antimicrobial activity of novel oxysterols from lanosterol”, Tetrahedron, vol. 69, no. 52, pp. 11155-11163, 2013.
B. B. Shingate, Liazra, B. G., Salunke, D. B., Pore, V. S., Shirazi, F., and Deshpande, M. V., “Stereoselective synthesis and antimicrobial activity of steroidal C-20 tertiary alcohols with thiazole/pyridine side chain”, European Journal of Medicinal Chemistry, vol. 46, no. 9, pp. 3681-3689, 2011.
B. B. Shingate, Hazra, B. G., Pore, V. S., Gonnade, R. G., and Bhadbhade, M. M., “Stereoselective syntheses of unnatural steroidal C(20R) aldehydes by ionic hydrogenation of C-20 tertiary alcohols”, Tetrahedron Letters, vol. 47, no. 52, pp. 9343-9347, 2006.
R
B. B. Shingate, Hazra, B. G., Salunke, D. B., and Pore, V. S., “RuCl3-TBHP mediated allylic oxidation of Delta(8(9)) lanosterol derivatives”, Tetrahedron Letters, vol. 52, no. 45, pp. 6007-6010, 2011.
Q
D. D. Subhedar, Shaikh, M. H., Shingate, B. B., Nawale, L., Sarkar, D., Khedkar, V. M., Khan, F. A. Kalam, and Sangshetti, J. N., “Quinolidene-rhodanine conjugates: facile synthesis and biological evaluation”, European Journal of Medicinal Chemistry, vol. 125, pp. 385–399, 2017.
D. D. Subhedar, Shaikh, M. H., Nawale, L. U., Sarkar, D., Khedkar, V. M., and Shingate, B. B., “Quinolidene based monocarbonyl curcumin analogues as promising antimycobacterial agents: synthesis and molecular docking study”, Bioorganic & medicinal chemistry letters, vol. 27, no. 4, pp. 922-928, 2017.
N
D. D. Subhedar, Shaikh, M. H., Shingate, B. B., Nawale, L., Sarkar, D., and Khedkar, V. M., “Novel tetrazoloquinoline-thiazolidinone conjugates as possible antitubercular agents: synthesis and molecular docking”, Medchemcomm, vol. 7, no. 9, pp. 1832-1848, 2016.
D. D. Subhedar, Shaikh, M. H., Nawale, L., Yeware, A., Sarkar, D., Khan, F. A. Kalam, Sangshetti, J. N., and Shingate, B. B., “Novel tetrazoloquinoline-rhodanine conjugates: highly efficient synthesis and biological evaluation”, Bioorganic & Medicinal Chemistry Letters, vol. 26, no. 9, pp. 2278-2283, 2016.
M. H. Shaikh, Subhedar, D., Nawale, L., Sarkar, D., Khan, F. A. Kalam, Sangshetti, J., and Shingate, B. B., “Novel benzylidenehydrazide-1,2,3-triazole conjugates as antitubercular agents: synthesis and molecular docking”, Mini Reviews in Medicinal Chemistry, vol. 18, 2018.
A. B. Danne, ,, Sangshetti, J. N., Khedkar, V. M., and Shingate, B. B., “New 1,2,3-triazole-appended bis-pyrazoles: synthesis, bioevaluation, and molecular docking”, ACS Omega, vol. 6, no. 38, pp. 24879-24890, 2021.
M
S. S. Sonar, Sadaphal, S. A., Pawar, S. S., Shingate, B. B., and Shingare, M. S., “Microwave assisted convenient synthesis of quino[2,3-b][1,5]benzoxazepines”, Chinese Chemical Letters, vol. 20, no. 5, pp. 557-561, 2009.
I
B. B. Shingate and Hazra, B. G., “Ionic hydrogenation-directed stereoselective construction of C-20(H) stereogenic center in steroid side chains: Scope and limitations”, Tetrahedron, vol. 73 , no. 17, pp. 2396-2414, 2017.
F
D. D. Subhedar, Shaikh, M. H., Khan, F. A. Kalam, Sangshetti, J. N., Khedkar, V. M., and Shingate, B. B., “Facile synthesis of new N-sulfonamidyl-4-thiazolidinone derivatives and their biological evaluation”, New Journal of Chemistry, vol. 40, no. 4, pp. 3047-3058, 2016.
D. D. Subhedar, Shaikh, M. H., Arkile, M. A., Yeware, A., Sarkar, D., and Shingate, B. B., “Facile synthesis of 1,3-thiazolidin-4-ones as antitubercular agents”, Bioorganic & Medicinal Chemistry Letters, vol. 26, no. 7, pp. 1704-1708, 2016.
D. D. Subhedar, Shaikh, M. H., Tupe, S. G., Deshpande, M. V., Khedkar, V. M., Jha, P. C., and Shingate, B. B., “Facile and solvent-free domino synthesis of new quinolidinyl-2,4-thiazolidinones: antifungal activityand molecular docking”, Mini-Reviews in Medicinal Chemistry, vol. 18, no. 7, pp. 622-630, 2018.
E
D. D. Subhedar, Shaikh, M. H., Nawale, L., Yeware, A., Sarkar, D., and Shingate, B. B., “[Et3NH][HSO4] catalyzed efficient synthesis of 5-arylidene-rhodanine conjugates and their antitubercular activity”, Research on Chemical Intermediates, vol. 42, no. 8, pp. 6607-6626, 2016.
D
D. D. Subhedar, Shaikh, M. H., Nagargoje, A. A., Sarkar, D., Khedkar, V. M., and Shingate, B. B., “[DBUH][OAc]-catalyzed domino synthesis of novel benzimidazole incorporated 3,5-Bis (Arylidene)-4-piperidones as potential antitubercular agents”, Polycyclic Aromatic Compounds, vol. 42, no. 10, pp. 7010-7024, 2022.
C
B. B. Shingate and Hazra, B. G., “Concise account of various approaches for stereoselective construction of the C-20(H) stereogenic center in steroid side chain”, Chemical Reviews, vol. 114, no. 12, pp. 6349-6382, 2014.
A
S. S. Sonar, Kategaonkar, A. H., Ware, M. N., Gill, C. H., Shingate, B. B., and Shingare, M. S., “Ammonium metavanadate: an effective catalyst for synthesis of alpha-hydroxyphosphonates”, Arkivoc, pp. 138-148, 2009.
D. D. Subhedar, Shaikh, M. H., Nagargoje, A. A., V. Akolkar, S., Bhansali, S. G., Sarkar, D., and Shingate, B. B., “Amide-linked monocarbonyl curcumin analogues: efficient synthesis, antitubercular activity and molecular docking study”, Polycyclic Aromatic Compounds, vol. 45, no. 5, pp. 2655-2671, 2022.
S. S. Sonar, Sadaphal, S. A., Shitole, N. N., Jogdand, N. R., Shingate, B. B., and Shingare, M. S., “Alum catalyzed convenient synthesis of quino [2,3-b][1,5]benzoxazepine alpha-aminophosphonate derivatives”, Bulletin of the Korean Chemical Society, vol. 30, no. 8, pp. 1711-1714, 2009.
S. S. Sonar, Shelke, K. F., Kakade, G. K., Shingate, B. B., and Shingare, M. S., “Alum: an efficient catalyst for one-pot synthesis of alpha-aminophosphonates”, Chinese Chemical Letters, vol. 20, no. 9, pp. 1042-1046, 2009.
1
M. H. Shaikh, Subhedar, D. D., Nawale, L., Sarkar, D., Khan, F. A. Kalam, Sangshetti, J. N., and Shingate, B. B., “1,2,3-Triazole derivatives as antitubercular agents: synthesis, biological evaluation and molecular docking study”, MedChemComm, vol. 6, no. 6, pp. 1104-1116, 2015.