Year |
Citation |
Score |
2020 |
Patel AR, Sereda G, Banerjee S. Synthesis, Characterization and Applications of Spinel Cobaltite Nanomaterials. Current Pharmaceutical Biotechnology. PMID 33208070 DOI: 10.2174/1389201021666201117122002 |
0.627 |
|
2020 |
Verma PR, Khan F, Banerjee S. Salvadora persica root extract-mediated fabrication of ZnO nanoparticles and characterization Inorganic and Nano-Metal Chemistry. 1-7. DOI: 10.1080/24701556.2020.1793355 |
0.339 |
|
2020 |
Ambati SR, Patel JL, Gudala S, Chandrakar K, Penta S, Mahapatra SP, Banerjee S. Synthesis of novel coumarinyl-pyrido[2,3-d]pyrimidine-2,4-diones using task-specific magnetic ionic liquid, [AcMIm]FeCl4 as catalyst Synthetic Communications. 50: 104-111. DOI: 10.1080/00397911.2019.1686526 |
0.381 |
|
2020 |
Patel G, Patel AR, Banerjee S. Visible light-emitting diode light-driven one-pot four component synthesis of poly-functionalized imidazoles under catalyst- and solvent-free conditions New Journal of Chemistry. 44: 13295-13300. DOI: 10.1039/D0Nj02527E |
0.443 |
|
2020 |
Asatkar A, Lambat TL, Mahmood S, Mondal A, Singh M, Banerjee S. Facile protocol for the synthesis of benzothiazole, benzoxazole and N-benzimidazole derivatives using rice husk derived chemically activated carbon Materials Today: Proceedings. 29: 738-742. DOI: 10.1016/J.Matpr.2020.04.510 |
0.404 |
|
2020 |
Asatkar A, Saha A, Lambat TL, Singh M, Banerjee S. Biomass rice husk derived activated carbon catalyzed synthesis of 5-aryl-1,2,4-triazolidine-3-thione derivatives under metal-free aqueous medium Materials Today: Proceedings. 29: 698-703. DOI: 10.1016/J.Matpr.2020.04.127 |
0.47 |
|
2020 |
Patel G, Patel AR, Lambat TL, Mahmood SH, Banerjee S. Rice husk derived nano-NiFe2O4@CAGC-catalyzed direct oxidation of toluene to benzyl benzoate under visible LED light Flatchem. 21: 100163. DOI: 10.1016/J.Flatc.2020.100163 |
0.448 |
|
2019 |
Lambat TL, Chaudhary RG, Abdala AA, Mishra RK, H Mahmood S, Banerjee S. Mesoporous PbO nanoparticle-catalyzed synthesis of arylbenzodioxy xanthenedione scaffolds under solvent-free conditions in a ball mill. Rsc Advances. 9: 31683-31690. PMID 35527919 DOI: 10.1039/c9ra05903b |
0.416 |
|
2019 |
Lambat TL, Abdala AA, Mahmood S, Ledade PV, Chaudhary RG, Banerjee S. Sulfamic acid promoted one-pot multicomponent reaction: a facile synthesis of 4-oxo-tetrahydroindoles under ball milling conditions Rsc Advances. 9: 39735-39742. DOI: 10.1039/C9Ra08478A |
0.358 |
|
2019 |
Lambat TL, Chaudhary RG, Abdala AA, Mishra RK, H. Mahmood S, Banerjee S. Mesoporous PbO nanoparticle-catalyzed synthesis of arylbenzodioxy xanthenedione scaffolds under solvent-free conditions in a ball mill Rsc Advances. 9: 31683-31690. DOI: 10.1039/C9Ra05903B |
0.488 |
|
2018 |
Saha A, Payra S, Selvaratnam B, Bhattacharya S, Pal S, Koodali RT, Banerjee S. Hierarchical Mesoporous RuO2/Cu2O Nanoparticle-Catalyzed Oxidative Homo/Hetero Azo-Coupling of Anilines Acs Sustainable Chemistry & Engineering. 6: 11345-11352. DOI: 10.1021/Acssuschemeng.8B01179 |
0.718 |
|
2018 |
Singha S, Saha A, Goswami S, Dey SK, Payra S, Banerjee S, Kumar S, Saha R. A Metal–Organic Framework to CuO Nanospheres of Uniform Morphology for the Synthesis of α-Aminonitriles under Solvent-Free Condition along with Crystal Structure of the Framework Crystal Growth & Design. 18: 189-199. DOI: 10.1021/Acs.Cgd.7B01085 |
0.734 |
|
2018 |
Saha A, Wu C, Peng R, Koodali R, Banerjee S. Facile Synthesis of 1,3,5-Triarylbenzenes and 4-Aryl-NH
-1,2,3-Triazoles Using Mesoporous Pd-MCM-41 as Reusable Catalyst European Journal of Organic Chemistry. 2019: 104-111. DOI: 10.1002/Ejoc.201801290 |
0.405 |
|
2018 |
Payra S, Saha A, Banerjee S. On Water Cu@g‐C3N4 Catalyzed Synthesis of NH‐1,2,3‐Triazoles via [2+3] Cycloadditions of Nitroolefins/Alkynes and Sodium Azide Chemcatchem. 10: 5468-5474. DOI: 10.1002/Cctc.201801524 |
0.703 |
|
2017 |
Saha A, Payra S, Dutta D, Banerjee S. Acid-Functionalised Magnetic Ionic Liquid [AcMIm]FeCl as Catalyst for Oxidative Hydroxylation of Arylboronic Acids and Regioselective Friedel-Crafts Acylation. Chempluschem. 82: 1129-1134. PMID 31957327 DOI: 10.1002/Cplu.201700221 |
0.702 |
|
2017 |
Payra S, Saha A, Banerjee S. Recent Advances on Fe-Based Magnetic Nanoparticles in Organic Transformations Journal of Nanoscience and Nanotechnology. 17: 4432-4448. DOI: 10.1166/Jnn.2017.14195 |
0.689 |
|
2017 |
Saha A, Payra S, Banerjee S. Synthesis of smart bimetallic nano-Cu/Ag@SiO2 for clean oxidation of alcohols New Journal of Chemistry. 41: 13377-13381. DOI: 10.1039/C7Nj02062G |
0.745 |
|
2016 |
Saha A, Payra S, Banerjee S. In-water facile synthesis of poly-substituted 6-arylamino pyridines and 2-pyrrolidone derivatives using tetragonal nano-ZrO2 as reusable catalyst Rsc Advances. 6: 101953-101959. DOI: 10.1039/C6Ra24367C |
0.774 |
|
2016 |
Payra S, Saha A, Banerjee S. On-water magnetic NiFe2O4 nanoparticle-catalyzed Michael additions of active methylene compounds, aromatic/aliphatic amines, alcohols and thiols to conjugated alkenes Rsc Advances. 6: 95951-95956. DOI: 10.1039/C6Ra21160G |
0.74 |
|
2016 |
Payra S, Saha A, Banerjee S. Nano-NiFe2O4 as an efficient catalyst for regio- and chemoselective transfer hydrogenation of olefins/alkynes and dehydrogenation of alcohols under Pd-/Ru-free conditions Rsc Advances. 6: 52495-52499. DOI: 10.1039/C6Ra09659J |
0.706 |
|
2016 |
Payra S, Saha A, Guchhait S, Banerjee S. Direct CuO nanoparticle-catalyzed synthesis of poly-substituted furans: Via oxidative C-H/C-H functionalization in aqueous medium Rsc Advances. 6: 33462-33467. DOI: 10.1039/C6Ra04181G |
0.756 |
|
2016 |
Payra S, Saha A, Wu C, Selvaratnam B, Dramstad T, Mahoney L, Verma SK, Thareja S, Koodali R, Banerjee S. Fe–SBA-15 catalyzed synthesis of 2-alkoxyimidazo[1,2-a]pyridines and screening of their in silico selectivity and binding affinity to biological targets New Journal of Chemistry. 40: 9753-9760. DOI: 10.1039/C6Nj02134D |
0.676 |
|
2016 |
Payra S, Saha A, Banerjee S. Nano-NiFe2O4 catalyzed microwave assisted one-pot regioselective synthesis of novel 2-alkoxyimidazo[1,2-a]pyridines under aerobic conditions Rsc Advances. 6: 12402-12407. DOI: 10.1039/C5Ra25540F |
0.751 |
|
2015 |
Saha A, Payra S, Banerjee S. On water synthesis of pyran–chromenes via a multicomponent reactions catalyzed by fluorescent t-ZrO2 nanoparticles Rsc Advances. 5: 101664-101671. DOI: 10.1039/C5Ra19290K |
0.733 |
|
2015 |
Saha A, Payra S, Verma SK, Mandal M, Thareja S, Banerjee S. In silico binding affinity to cyclooxygenase-II and green synthesis of benzylpyrazolyl coumarin derivatives Rsc Advances. 5: 100978-100983. DOI: 10.1039/C5Ra16643H |
0.695 |
|
2015 |
Banerjee S. The remarkable catalytic activity of ultra-small free-CeO2 nanoparticles in selective carbon–carbon bond formation reactions in water at room temperature New Journal of Chemistry. 39: 5350-5353. DOI: 10.1039/C5Nj00500K |
0.477 |
|
2015 |
Saha A, Payra S, Banerjee S. One-pot multicomponent synthesis of highly functionalized bio-active pyrano[2,3-c]pyrazole and benzylpyrazolyl coumarin derivatives using ZrO2 nanoparticles as a reusable catalyst Green Chemistry. 17: 2859-2866. DOI: 10.1039/C4Gc02420F |
0.77 |
|
2014 |
Payra S, Saha A, Peng R, Wu CM, Koodali RT, Banerjee S. Expeditious one-pot three component synthesis of N-aryl dithiocarbamate derivatives using mesoporous Cu-materials Tetrahedron Letters. DOI: 10.1016/J.Tetlet.2015.01.158 |
0.716 |
|
2014 |
Banerjee S, Payra S, Saha A, Sereda G. ZnO nanoparticles: a green efficient catalyst for the room temperature synthesis of biologically active 2-aryl-1,3-benzothiazole and 1,3-benzoxazole derivatives Tetrahedron Letters. 55: 5515-5520. DOI: 10.1016/J.Tetlet.2014.07.123 |
0.816 |
|
2013 |
Banerjee S, Saha A. Free-ZnO nanoparticles: a mild, efficient and reusable catalyst for the one-pot multicomponent synthesis of tetrahydrobenzo[b]pyran and dihydropyrimidone derivatives New Journal of Chemistry. 37: 4170-4175. DOI: 10.1039/C3Nj00723E |
0.487 |
|
2012 |
Banerjee S, Adak L, Ranu BC. Ionic liquid/PPh3 promoted cleavage of diphenyl disulfide and diselenide: a straight-forward metal-free one-pot route to the synthesis of unsymmetrical sulfides and selenides Tetrahedron Letters. 53: 2149-2152. DOI: 10.1016/J.Tetlet.2012.02.047 |
0.569 |
|
2012 |
Peng R, Banerjee S, Sereda G, Koodali RT. TiO 2-SiO 2 mixed oxides: Organic ligand templated controlled deposition of titania and their photocatalytic activities for hydrogen production International Journal of Hydrogen Energy. 37: 17009-17018. DOI: 10.1016/J.Ijhydene.2012.07.047 |
0.619 |
|
2011 |
Banerjee S, Khatri H, Balasanthiran V, Koodali RT, Sereda G. Cross-Coupling Using Mesoporous Pd-MCM-48 Synfacts. 2011: 1139-1139. DOI: 10.1055/S-0030-1261088 |
0.582 |
|
2011 |
Banerjee S, Horn A, Khatri H, Sereda G. A green one-pot multicomponent synthesis of 4H-pyrans and polysubstituted aniline derivatives of biological, pharmacological, and optical applications using silica nanoparticles as reusable catalyst Tetrahedron Letters. 52: 1878-1881. DOI: 10.1016/J.Tetlet.2011.02.031 |
0.709 |
|
2011 |
Banerjee S, Khatri H, Balasanthiran V, Koodali RT, Sereda G. Synthesis of substituted acetylenes, aryl-alkyl ethers, 2-alkene-4-ynoates and nitriles using heterogeneous mesoporous Pd-MCM-48 as reusable catalyst Tetrahedron. 67: 5717-5724. DOI: 10.1016/J.Tet.2011.05.132 |
0.71 |
|
2010 |
Banerjee S, Balasanthiran V, Koodali RT, Sereda GA. Pd-MCM-48: a novel recyclable heterogeneous catalyst for chemo- and regioselective hydrogenation of olefins and coupling reactions. Organic & Biomolecular Chemistry. 8: 4316-21. PMID 20668769 DOI: 10.1039/C0Ob00183J |
0.693 |
|
2010 |
Rajpara V, Banerjee S, Sereda G. Alkylation of Arenes with Fe3O4 Nanoparticles onOxidized Graphite Synfacts. 2010: 1320-1320. DOI: 10.1055/S-0030-1258821 |
0.657 |
|
2010 |
Rajpara V, Banerjee S, Sereda G. Iron Oxide Nanoparticles Grownon Carboxy-Functionalized Graphite: An Efficient ReusableCatalyst for Alkylation of Arenes Synthesis. 2010: 2835-2840. DOI: 10.1055/S-0029-1218851 |
0.78 |
|
2010 |
Banerjee S, Das J, Alvarez RP, Santra S. Silica nanoparticles as a reusable catalyst: A straightforward route for the synthesis of thioethers, thioesters, vinyl thioethers and thio-Michael adducts under neutral reaction conditions New Journal of Chemistry. 34: 302-306. DOI: 10.1039/B9Nj00399A |
0.531 |
|
2009 |
Banerjee S, Das J, Santra S. Silica Nanoparticles Catalyzed Addition of Thiols to Alkenesand Alkynes Synfacts. 2009: 347-347. DOI: 10.1055/S-0028-1087738 |
0.426 |
|
2009 |
Banerjee S, Sereda G. One-step, three-component synthesis of highly substituted pyridines using silica nanoparticle as reusable catalyst Tetrahedron Letters. 50: 6959-6962. DOI: 10.1016/J.Tetlet.2009.09.137 |
0.723 |
|
2009 |
Banerjee S, Santra S. Remarkable catalytic activity of silica nanoparticle in the bis-Michael addition of active methylene compounds to conjugated alkenes Tetrahedron Letters. 50: 2037-2040. DOI: 10.1016/J.Tetlet.2009.01.154 |
0.447 |
|
2009 |
Banerjee S, Das J, Santra S. Native silica nanoparticle catalyzed anti-Markovnikov addition of thiols to inactivated alkenes and alkynes: a new route to linear and vinyl thioethers Tetrahedron Letters. 50: 124-127. DOI: 10.1016/J.Tetlet.2008.10.110 |
0.494 |
|
2008 |
Ranu BC, Adak L, Banerjee S. Ionic liquid promoted interrupted Feist–Benary reaction with high diastereoselectivity Tetrahedron Letters. 49: 4613-4617. DOI: 10.1016/J.Tetlet.2008.05.083 |
0.552 |
|
2008 |
Ranu BC, Saha A, Banerjee S. Catalysis by Ionic Liquids: Significant Rate Acceleration with the Use of [pmIm]Br in the Three-Component Synthesis of Dithiocarbamates European Journal of Organic Chemistry. 2008: 519-523. DOI: 10.1002/Ejoc.200700842 |
0.579 |
|
2007 |
Ranu BC, Banerjee S. Homocoupling of Terminal Alkynes to 1,4-Disubstituted 1,3-Diynes Promoted by Copper(I) Iodide and a Task Specific Ionic Liquid, [bmim]OH — A Green Procedure. Cheminform. 38. DOI: 10.2174/157017806778559518 |
0.533 |
|
2007 |
Ranu BC, Adak L, Banerjee S. Efficient Regio- and Stereoselective Cleavage of Aziridines and Epoxides Using an Ionic Liquid as Reagent and Reaction Medium. Cheminform. 38. DOI: 10.1139/V07-040 |
0.594 |
|
2007 |
Ranu BC, Banerjee S, Gupta J. Ionic Liquid–Promoted Stereoselective Synthesis of (Z)‐Vinyl Bromides by [bmIm]OH under Organic Solvent–Free Conditions: A Green Approach Synthetic Communications. 37: 2869-2876. DOI: 10.1080/00397910701471386 |
0.576 |
|
2007 |
Ranu BC, Adak L, Banerjee S. Halogenation of Carbonyl Compounds by an Ionic Liquid, [AcMIm]X, and Ceric Ammonium Nitrate (CAN) Australian Journal of Chemistry. 60: 358. DOI: 10.1071/Ch07061 |
0.527 |
|
2007 |
Ranu BC, Mandal T, Banerjee S, Dey SS. Ionic Liquid Promoted Regio- and Stereo-Selective Thiolysis of Epoxides—A Simple and Green Approach to β-Hydroxy- and β-Keto Sulfides Australian Journal of Chemistry. 60: 278. DOI: 10.1071/Ch06434 |
0.535 |
|
2007 |
Ranu BC, Banerjee S, Adak L. Regioselective cross-coupling of allylindium reagents with activated benzylic bromides—a simple and efficient procedure for the synthesis of terminal alkenes Tetrahedron Letters. 48: 7374-7379. DOI: 10.1016/J.Tetlet.2007.08.025 |
0.593 |
|
2007 |
Ranu BC, Banerjee S. Significant rate acceleration of the aza-Michael reaction in water Tetrahedron Letters. 48: 141-143. DOI: 10.1016/J.Tetlet.2006.10.142 |
0.549 |
|
2007 |
Ranu BC, Banerjee S, Jana R. Ionic liquid as catalyst and solvent: the remarkable effect of a basic ionic liquid, [bmIm]OH on Michael addition and alkylation of active methylene compounds Tetrahedron. 63: 776-782. DOI: 10.1016/J.Tet.2006.10.077 |
0.711 |
|
2006 |
Ranu BC, Chattopadhyay K, Banerjee S. Indium(I) iodide promoted cleavage of diphenyl diselenide and disulfide and subsequent palladium(0)-catalyzed condensation with vinylic bromides. A simple one-pot synthesis of vinylic selenides and sulfides. The Journal of Organic Chemistry. 71: 423-5. PMID 16388676 DOI: 10.1021/Jo052087I |
0.58 |
|
2006 |
Ranu BC, Banerjee S, Das A. Catalysis by Ionic Liquids: Cyclopropyl Carbinyl Rearrangements Catalyzed by [pmim]Br under Organic Solvent Free Conditions. Cheminform. 37. DOI: 10.1016/J.Tetlet.2005.12.003 |
0.54 |
|
2006 |
Ranu BC, Banerjee S. Indium Triflate Catalyzed Rearrangement of Aryl-Substituted Cyclopropyl Carbinols to 1,4-Disubstituted 1,3-Butadienes European Journal of Organic Chemistry. 2006: 3012-3015. DOI: 10.1002/Ejoc.200600037 |
0.553 |
|
2005 |
Ranu BC, Banerjee S. Ionic liquid as catalyst and reaction medium. The dramatic influence of a task-specific ionic liquid, [bmIm]OH, in Michael addition of active methylene compounds to conjugated ketones, carboxylic esters, and nitriles. Organic Letters. 7: 3049-52. PMID 15987202 DOI: 10.1021/Ol051004H |
0.563 |
|
2005 |
Ranu BC, Banerjee S. Ionic liquid as reagent. A green procedure for the regioselective conversion of epoxides to vicinal-halohydrins using [AcMIm]X under catalyst- and solvent-free conditions. The Journal of Organic Chemistry. 70: 4517-9. PMID 15903336 DOI: 10.1021/Jo0500885 |
0.584 |
|
2004 |
Ranu BC, Banerjee S, Das A. Selective reductive cleavage of 2,3-epoxybromides by the InCl3–NaBH4 reagent system Tetrahedron Letters. 45: 8579-8581. DOI: 10.1016/J.Tetlet.2004.09.120 |
0.539 |
|
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