Year |
Citation |
Score |
2024 |
Peng K, Anmangandla A, Jana S, Jin Y, Lin H. Iso-ADP-Ribose Fluorescence Polarization Probe for the Screening of RNF146 WWE Domain Inhibitors. Acs Chemical Biology. PMID 38237916 DOI: 10.1021/acschembio.3c00512 |
0.454 |
|
2023 |
Smith MR, Zhang L, Jin Y, Yang M, Bade A, Gillis KD, Jana S, Bypaneni RN, Glass TE, Lin H. A Turn-On Fluorescent Amino Acid Sensor Reveals Chloroquine's Effect on Cellular Amino Acids via Inhibiting Cathepsin L. Acs Central Science. 9: 980-991. PMID 37252359 DOI: 10.1021/acscentsci.2c01325 |
0.441 |
|
2023 |
Anmangandla A, Jana S, Peng K, Wallace SD, Bagde SR, Drown BS, Xu J, Hergenrother PJ, Fromme JC, Lin H. A Fluorescence Polarization Assay for Macrodomains Facilitates the Identification of Potent Inhibitors of the SARS-CoV-2 Macrodomain. Acs Chemical Biology. PMID 37126856 DOI: 10.1021/acschembio.3c00092 |
0.451 |
|
2023 |
O'Brien C, Ling T, Berman JM, Culp-Hill R, Reisz JA, Rondeau V, Jahangiri S, St-Germain J, Macwan V, Astori A, Zeng A, Hong JY, Li M, Yang M, Jana S, et al. Simultaneous inhibition of Sirtuin 3 and cholesterol homeostasis targets acute myeloid leukemia stem cells by perturbing fatty acid β-oxidation and inducing lipotoxicity. Haematologica. PMID 37021547 DOI: 10.3324/haematol.2022.281894 |
0.459 |
|
2021 |
Bag S, Jana S, Pradhan S, Bhowmick S, Goswami N, Sinha SK, Maiti D. Imine as a linchpin approach for meta-C-H functionalization. Nature Communications. 12: 1393. PMID 33654108 DOI: 10.1038/s41467-021-21633-2 |
0.771 |
|
2020 |
Achar TK, Maiti S, Jana S, Maiti D. Transition Metal Catalyzed Enantioselective C(sp2)–H Bond Functionalization Acs Catalysis. 10: 13748-13793. DOI: 10.1021/acscatal.0c03743 |
0.376 |
|
2019 |
Kankanala R, Biswas JP, Jana S, Achar TK, Porey S, Maiti D. Co-ordination assisted distal C-H alkylation of fused heterocycles. Angewandte Chemie (International Ed. in English). PMID 31336005 DOI: 10.1002/Anie.201907544 |
0.551 |
|
2019 |
Brochetta M, Borsari T, Bag S, Jana S, Maiti S, Porta A, Werz DB, Zanoni G, Maiti D. Direct meta-C-H Perfluoroalkenylation of Arenes Enabled by a Cleavable Pyrimidine-Based Template. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31215707 DOI: 10.1002/Chem.201902811 |
0.813 |
|
2019 |
Jana S, Verma A, Rathore V, Kumar S. Synthesis of Novel C
2-Symmetric Sulfur-Based Catalysts: Asymmetric Formation of Halo- and Seleno-Functionalized Normal- and Medium-Sized Rings Synlett. 30: 1667-1672. DOI: 10.1055/S-0037-1610715 |
0.772 |
|
2017 |
Jana S, Verma A, Kadu R, Kumar S. Visible-light-induced oxidant and metal-free dehydrogenative cascade trifluoromethylation and oxidation of 1,6-enynes with water. Chemical Science. 8: 6633-6644. PMID 28989690 DOI: 10.1039/C7Sc02556D |
0.692 |
|
2016 |
Verma A, Jana S, Durga Prasad C, Yadav A, Kumar S. Organoselenium and DMAP co-catalysis: regioselective synthesis of medium-sized halolactones and bromooxepanes from unactivated alkenes. Chemical Communications (Cambridge, England). PMID 26906914 DOI: 10.1039/C5Cc10245F |
0.676 |
|
2015 |
Jana S, Ashokan A, Kumar S, Verma A, Kumar S. Copper-catalyzed trifluoromethylation of alkenes: synthesis of trifluoromethylated benzoxazines. Organic & Biomolecular Chemistry. 13: 8411-5. PMID 26166814 DOI: 10.1039/C5Ob01196E |
0.74 |
|
2015 |
Kumar S, Rathore V, Verma A, Prasad ChD, Kumar A, Yadav A, Jana S, Sattar M, Meenakshi, Kumar S. KO(t)Bu-mediated aerobic transition-metal-free regioselective β-arylation of indoles: synthesis of β-(2-/4-nitroaryl)-indoles. Organic Letters. 17: 82-5. PMID 25496238 DOI: 10.1021/Ol503274Z |
0.746 |
|
2015 |
Verma A, Patel S, Meenakshi, Kumar A, Yadav A, Kumar S, Jana S, Sharma S, Prasad ChD, Kumar S. Transition metal free intramolecular selective oxidative C(sp3)-N coupling: synthesis of N-aryl-isoindolinones from 2-alkylbenzamides. Chemical Communications (Cambridge, England). 51: 1371-4. PMID 25487732 DOI: 10.1039/C4Cc08717H |
0.736 |
|
2014 |
Kumar A, Yadav A, Verma A, Jana S, Sattar M, Kumar S, Prasad ChD, Kumar S. Chemoselective arylation of phenols with bromo-nitroarenes: synthesis of nitro-biaryl-ols and their conversion into benzofurans and carbazoles. Chemical Communications (Cambridge, England). 50: 9481-4. PMID 25007753 DOI: 10.1039/C4Cc03090G |
0.685 |
|
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