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Tapan Kumar Kuilya - Publications

Affiliations: 
2017 Indian Association for the Cultivation of Science 
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8 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2022 Bose C, Das U, Kuilya TK, Mondal J, Bhadra J, Banerjee P, Goswami RK, Sinha S. Cananginone Abrogates EMT in Breast Cancer Cells through Hedgehog Signaling. Chemistry & Biodiversity. e202100823. PMID 35298074 DOI: 10.1002/cbdv.202100823  0.636
2018 Chatterjee S, Kuilya TK, Goswami RK. Studies Directed toward the Stereoselective Synthesis of Cytospolide E. Acs Omega. 3: 1041-1059. PMID 31457947 DOI: 10.1021/acsomega.7b01893  0.696
2018 Kuilya TK, Das S, Saha D, Goswami RK. Studies toward the synthesis of strevertenes A and G: stereoselective construction of C-C segments of the molecules. Organic & Biomolecular Chemistry. PMID 30191223 DOI: 10.1039/C8Ob01754A  0.649
2017 Kuilya TK, Goswami RK. Stereoselective Total Synthesis of Carolacton. Organic Letters. 19: 2366-2369. PMID 28436677 DOI: 10.1021/Acs.Orglett.7B00903  0.757
2016 Kuilya TK, Goswami RK. Total synthesis of cananginone C and structural revision of debilisone A. Organic & Biomolecular Chemistry. 14: 8789-8799. PMID 27714187 DOI: 10.1039/C6Ob01671E  0.75
2015 Das S, Kuilya TK, Goswami RK. Asymmetric Total Synthesis of Bioactive Natural Lipid Mycalol. The Journal of Organic Chemistry. 80: 6467-89. PMID 25992780 DOI: 10.1021/Acs.Joc.5B00972  0.709
2014 Kuilya TK, Chatterjee S, Goswami RK. Stereoselective total synthesis of cananginones (D-I) using Ireland-Claisen rearrangement as a key step Tetrahedron. 70: 2905-2918. DOI: 10.1016/J.Tet.2014.03.028  0.751
2014 Kuilya TK, Chatterjee S, Goswami RK. ChemInform Abstract: Stereoselective Total Synthesis of Cananginones (D-I) Using Ireland-Claisen Rearrangement as a Key Step. Cheminform. 45: no-no. DOI: 10.1002/CHIN.201438212  0.727
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