| Year |
Citation |
Score |
| 2022 |
Kumar D, Sharma H, Saha N, Chakraborti AK. Domino synthesis of functionalized pyridine carboxylates under gallium catalysis: Unravelling the reaction pathway and the role of the nitrogen source counter anion. Chemistry, An Asian Journal. PMID 35608137 DOI: 10.1002/asia.202200304 |
0.766 |
|
| 2020 |
Vaidya GN, Rana P, Venkatesh A, Chatterjee DR, Contractor D, Satpute DP, Nagpure M, Jain A, Kumar D. Paradigm shift of "classical" HDAC inhibitors to "hybrid" HDAC inhibitors in therapeutic interventions. European Journal of Medicinal Chemistry. 112844. PMID 33143937 DOI: 10.1016/J.Ejmech.2020.112844 |
0.595 |
|
| 2019 |
Vaidya GN, Khan A, Verma H, Kumar S, Kumar D. Structure Ligation Relationship of Amino Acids for the Amination Cross-Coupling Reactions. The Journal of Organic Chemistry. PMID 30734563 DOI: 10.1021/Acs.Joc.8B03214 |
0.683 |
|
| 2019 |
Vaidya GN, Fiske S, Verma H, Lokhande SK, Kumar D. A micellar catalysis strategy applied to the Pd-catalyzed C–H arylation of indoles in water Green Chemistry. 21: 1448-1454. DOI: 10.1039/C8Gc03413C |
0.677 |
|
| 2018 |
Vemula SR, Kumar D, Cook GR. Bismuth-Catalyzed Synthesis of 2-Substituted Quinazolinones. Tetrahedron Letters. 59: 3801-3805. PMID 31274936 DOI: 10.1016/J.Tetlet.2018.09.014 |
0.68 |
|
| 2016 |
Kumar D, Vemula SR, Balasubramanian N, Cook GR. Indium-Mediated Stereoselective Allylation. Accounts of Chemical Research. PMID 27700084 DOI: 10.1021/Acs.Accounts.6B00362 |
0.77 |
|
| 2016 |
Jadhavar PS, Dhameliya TM, Vaja MD, Kumar D, Sridevi JP, Yogeeswari P, Sriram D, Chakraborti AK. Synthesis, biological evaluation and structure-activity relationship of 2-styrylquinazolones as anti-tubercular agents. Bioorganic & Medicinal Chemistry Letters. PMID 27095514 DOI: 10.1016/J.Bmcl.2016.04.012 |
0.727 |
|
| 2016 |
Vemula SR, Kumar D, Cook GR. Palladium-Catalyzed Allylic Amidation with N-Heterocycles via sp3 C–H Oxidation Acs Catalysis. 6: 5295-5301. DOI: 10.1021/Acscatal.6B01818 |
0.685 |
|
| 2016 |
Kumar D, Vemula SR, Cook GR. Recent Advances in the Catalytic Synthesis of α-Ketoamides Acs Catalysis. 6: 4920-4945. DOI: 10.1021/Acscatal.6B01116 |
0.63 |
|
| 2016 |
Kumar D, Vemula SR, Cook GR. Merging C–H Bond Functionalization with Amide Alcoholysis: En Route to 2-Aminopyridines Acs Catalysis. 6: 3531-3536. DOI: 10.1021/Acscatal.6B00728 |
0.662 |
|
| 2016 |
Shard A, Rawat K, Sinha AK, Padwad Y, Kumar D. Divergent Synthesis of Styryl-Cinnamate Hybrid Analogues Inspired by the Natural Product Salvianolic Acid F as a Premise To Investigate Their Anticancer Activity and Its Metabolomic Profiling European Journal of Organic Chemistry. 2016: 5941-5949. DOI: 10.1002/Ejoc.201601104 |
0.303 |
|
| 2016 |
Tanwar B, Kumar D, Kumar A, Ansari MI, Qadri MM, Vaja MD, Singh M, Chakraborti AK. ChemInform Abstract: Friedlaender Annulation: Scope and Limitations of Metal Salt Lewis Acid Catalysts in Selectivity Control for the Synthesis of Functionalized Quinolines. Cheminform. 47. DOI: 10.1002/CHIN.201614146 |
0.741 |
|
| 2015 |
Kumar D, Jadhavar PS, Nautiyal M, Sharma H, Meena PK, Adane L, Pancholia S, Chakraborti AK. Convenient synthesis of 2,3-disubstituted quinazolin-4(3H)-ones and 2-styryl-3-substituted quinazolin-4(3H)-ones: Applications towards the synthesis of drugs Rsc Advances. 5: 30819-30825. DOI: 10.1039/C5Ra03888J |
0.808 |
|
| 2015 |
Tanwar B, Kumar D, Kumar A, Ansari MI, Qadri MM, Vaja MD, Singh M, Chakraborti AK. Friedländer annulation: scope and limitations of metal salt Lewis acid catalysts in selectivity control for the synthesis of functionalised quinolines New Journal of Chemistry. 39: 9824-9833. DOI: 10.1039/C5Nj02010G |
0.763 |
|
| 2015 |
Kumar D, Vemula SR, Cook GR. Highly chemo- and regioselective allylic substitution with tautomerizable heteroarenes Green Chemistry. 17: 4300-4306. DOI: 10.1039/C5Gc01028D |
0.629 |
|
| 2015 |
Tanwar B, Purohit P, Raju BN, Kumar D, Kommi DN, Chakraborti AK. An “all-water” strategy for regiocontrolled synthesis of 2-aryl quinoxalines Rsc Advances. 5: 11873-11883. DOI: 10.1039/C4Ra16568C |
0.781 |
|
| 2015 |
Kumar D, Kumar A, Qadri MM, Ansari MI, Gautam A, Chakraborti AK. In(OTf)3-catalyzed synthesis of 2-styryl quinolines: Scope and limitations of metal Lewis acids for tandem Friedländer annulation-Knoevenagel condensation Rsc Advances. 5: 2920-2927. DOI: 10.1039/C4Ra10613J |
0.76 |
|
| 2015 |
Vemula SR, Kumar D, Cook GR. N-Boc-glycine-assisted indium-mediated allylation reaction: A sustainable approach Tetrahedron Letters. 56: 3322-3325. DOI: 10.1016/J.Tetlet.2015.01.036 |
0.66 |
|
| 2015 |
Kumar D, Vemula SR, Cook GR. ChemInform Abstract: Highly Chemo- and Regioselective Allylic Substitution with Tautomerizable Heteroarenes. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201551168 |
0.301 |
|
| 2015 |
Vemula SR, Kumar D, Cook GR. ChemInform Abstract: N-Boc-Glycine-Assisted Indium-Mediated Allylation Reaction: A Sustainable Approach. Cheminform. 46: no-no. DOI: 10.1002/chin.201540134 |
0.612 |
|
| 2015 |
Tanwar B, Purohit P, Raju BN, Kumar D, Kommi DN, Chakraborti AK. ChemInform Abstract: An “All-Water” Strategy for Regiocontrolled Synthesis of 2-Aryl Quinoxalines. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201527223 |
0.814 |
|
| 2015 |
Kumar D, Kumar A, Qadri MM, Ansari MI, Gautam A, Chakraborti AK. ChemInform Abstract: In(OTf)3-Catalyzed Synthesis of 2-Styryl Quinolines: Scope and Limitations of Metal Lewis Acids for Tandem Friedlaender Annulation-Knoevenagel Condensation. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201523174 |
0.731 |
|
| 2014 |
Kamboj RC, Jindal P, Kumar D, Khullar S, Mandal SK. Synthesis of some benzofurooxepines' derivatives via [3+2] cycloaddition of epoxide with tethered alkyne: A photochemical approach Journal of Photochemistry and Photobiology a: Chemistry. 278: 31-38. DOI: 10.1016/j.jphotochem.2013.12.017 |
0.314 |
|
| 2014 |
Jadhavar PS, Kumar D, Purohit P, Pipaliya BV, Kumar A, Bhagat S, Chakraborti AK. Sustainable approaches towards the synthesis of quinoxalines Green Chemistry: Synthesis of Bioactive Heterocycles. 37-67. DOI: 10.1007/978-81-322-1850-0_2 |
0.773 |
|
| 2014 |
Kumar D, Sonawane M, Pujala B, Jain VK, Bhagat S, Chakraborti AK. ChemInform Abstract: Supported Protic Acid-Catalyzed Synthesis of 2,3-Disubstituted Thiazolidin-4-ones: Enhancement of the Catalytic Potential of Protic Acid by Adsorption on Solid Supports. Cheminform. 45: no-no. DOI: 10.1002/CHIN.201410145 |
0.793 |
|
| 2013 |
Kommi DN, Kumar D, Seth K, Chakraborti AK. Protecting group-free concise synthesis of (RS)/(S)-lubeluzole. Organic Letters. 15: 1158-61. PMID 23432765 DOI: 10.1021/Ol302601B |
0.806 |
|
| 2013 |
Kumar D, Seth K, Kommi DN, Bhagat S, Chakraborti AK. Surfactant micelles as microreactors for the synthesis of quinoxalines in water: Scope and limitations of surfactant catalysis Rsc Advances. 3: 15157-15168. DOI: 10.1039/C3Ra41038B |
0.807 |
|
| 2013 |
Kumar D, Sonawane M, Pujala B, Jain VK, Bhagat S, Chakraborti AK. Supported protic acid-catalyzed synthesis of 2,3-disubstituted thiazolidin-4-ones: Enhancement of the catalytic potential of protic acid by adsorption on solid supports Green Chemistry. 15: 2872-2884. DOI: 10.1039/C3Gc41218K |
0.815 |
|
| 2013 |
Kommi DN, Jadhavar PS, Kumar D, Chakraborti AK. “All-water” one-pot diverse synthesis of 1,2-disubstituted benzimidazoles: hydrogen bond driven ‘synergistic electrophile–nucleophile dual activation’ by water Green Chemistry. 15: 798. DOI: 10.1039/C3Gc37004F |
0.806 |
|
| 2013 |
Kommi DN, Kumar D, Chakraborti AK. “All water chemistry” for a concise total synthesis of the novel class anti-anginal drug (RS), (R), and (S)-ranolazine Green Chemistry. 15: 756. DOI: 10.1039/C3Gc36997H |
0.831 |
|
| 2013 |
Kumar D, Kommi DN, Chebolu R, Garg SK, Kumar R, Chakraborti AK. Selectivity control during the solid supported protic acids catalysed synthesis of 1,2-disubstituted benzimidazoles and mechanistic insight to rationalize selectivity Rsc Adv.. 3: 91-98. DOI: 10.1039/C2Ra21994H |
0.798 |
|
| 2013 |
Kommi DN, Kumar D, Chakraborti AK. ChemInform Abstract: “All Water Chemistry” for a Concise Total Synthesis of the Novel Class Antianginal Drug (RS), (R), and (S)-Ranolazine. Cheminform. 44: no-no. DOI: 10.1002/CHIN.201327167 |
0.774 |
|
| 2013 |
Kommi DN, Jadhavar PS, Kumar D, Chakraborti AK. ChemInform Abstract: “All-Water” One-Pot Diverse Synthesis of 1,2-Disubstituted Benzimidazoles: Hydrogen Bond Driven ′Synergistic Electrophile-Nucleophile Dual Activation′ by Water. Cheminform. 44: no-no. DOI: 10.1002/CHIN.201326114 |
0.796 |
|
| 2013 |
Kommi DN, Kumar D, Bansal R, Chebolu R, Chakraborti AK. ChemInform Abstract: “All-Water” Chemistry of Tandem N-Alkylation-Reduction-Condensation for Synthesis of N-Arylmethyl-2-substituted Benzimidazoles. Cheminform. 44: no-no. DOI: 10.1002/CHIN.201316089 |
0.788 |
|
| 2013 |
Kumar D, Kommi DN, Chopra P, Ansari MI, Chakraborti AK. ChemInform Abstract: L-Proline-Catalyzed Activation of Methyl Ketones or Active Methylene Compounds and DMF-DMA for Syntheses of (2E)-3-Dimethylamino-2-propen-1-ones. Cheminform. 44: no-no. DOI: 10.1002/CHIN.201314045 |
0.78 |
|
| 2012 |
Chebolu R, Kommi DN, Kumar D, Bollineni N, Chakraborti AK. Hydrogen-bond-driven electrophilic activation for selectivity control: scope and limitations of fluorous alcohol-promoted selective formation of 1,2-disubstituted benzimidazoles and mechanistic insight for rationale of selectivity. The Journal of Organic Chemistry. 77: 10158-67. PMID 23067292 DOI: 10.1021/Jo301793Z |
0.784 |
|
| 2012 |
Sarkar A, Raha Roy S, Kumar D, Madaan C, Rudrawar S, Chakraborti AK. Lack of correlation between catalytic efficiency and basicity of amines during the reaction of aryl methyl ketones with DMF-DMA: an unprecedented supramolecular domino catalysis. Organic & Biomolecular Chemistry. 10: 281-6. PMID 22057389 DOI: 10.1039/C1Ob06043K |
0.803 |
|
| 2012 |
Kommi DN, Kumar D, Bansal R, Chebolu R, Chakraborti AK. “All-water” chemistry of tandem N-alkylation–reduction–condensation for synthesis of N-arylmethyl-2-substituted benzimidazoles Green Chemistry. 14: 3329. DOI: 10.1039/C2Gc36377A |
0.795 |
|
| 2012 |
Kumar D, Kommi DN, Bollineni N, Patel AR, Chakraborti AK. Catalytic procedures for multicomponent synthesis of imidazoles: selectivity control during the competitive formation of tri- and tetrasubstituted imidazoles Green Chemistry. 14: 2038. DOI: 10.1039/C2Gc35277J |
0.83 |
|
| 2012 |
Kumar D, Kommi DN, Chopra P, Ansari MI, Chakraborti AK. L-proline-catalyzed activation of methyl ketones or active methylene compounds and DMF-DMA for syntheses of (2E)-3-dimethylamino-2- propen-1-ones European Journal of Organic Chemistry. 6407-6413. DOI: 10.1002/Ejoc.201200778 |
0.803 |
|
| 2012 |
Kumar D, Kommi DN, Bollineni N, Patel AR, Chakraborti AK. ChemInform Abstract: Catalytic Procedures for Multicomponent Synthesis of Imidazoles: Selectivity Control During the Competitive Formation of Tri- and Tetrasubstituted Imidazoles. Cheminform. 43: no-no. DOI: 10.1002/CHIN.201245147 |
0.806 |
|
| 2011 |
Parikh N, Kumar D, Roy SR, Chakraborti AK. Surfactant mediated oxygen reuptake in water for green aerobic oxidation: Mass-spectrometric determination of discrete intermediates to correlate oxygen uptake with oxidation efficiency Chemical Communications. 47: 1797-1799. PMID 21127798 DOI: 10.1039/C0Cc03166F |
0.746 |
|
| 2011 |
Chakraborti A, Bindal S, Kumar D, Kommi D, Bhatiya S. Efficient Organocatalytic Dual Activation Strategy for Preparing the Versatile Synthons (2E)-1-(Het)Aryl/styryl-3-(dimethylamino)prop-2-en-1-ones and α-(E)-[(Dimethylamino)methylene]cycloalkanones Synthesis. 2011: 1930-1935. DOI: 10.1055/S-0030-1260048 |
0.808 |
|
| 2011 |
Bindal S, Kumar D, Kommi DN, Bhatiya S, Chakraborti AK. ChemInform Abstract: Efficient Organocatalytic Dual Activation Strategy for Preparing the Versatile Synthons (2E)-1-(Het)Aryl/styryl-3-(dimethylamino)prop-2-en-1-ones and α-(E)-[(Dimethylamino)methylene]cycloalkanones. Cheminform. 42: no-no. DOI: 10.1002/CHIN.201146058 |
0.78 |
|
| 2009 |
Chakraborti AK, Roy SR, Kumar D, Chopra P. ChemInform Abstract: Catalytic Application of Room Temperature Ionic Liquids: [bmim][MeSO4] as a Recyclable Catalyst for Synthesis of Bis(indolyl)methanes: Ion-Fishing by MALDI-TOF-TOF MS and MS/MS Studies to Probe the Proposed Mechanistic Model of Catalysis. Cheminform. 40. DOI: 10.1002/CHIN.200907125 |
0.477 |
|
| 2008 |
Kumar D, Rudrawar S, Chakraborti AK. One-Pot Synthesis of 2-Substituted Benzoxazoles Directly from Carboxylic Acids Australian Journal of Chemistry. 61: 881. DOI: 10.1071/Ch08193 |
0.803 |
|
| 2008 |
Chakraborti A, Kumar D, Kumar R. Tetrafluoroboric Acid Adsorbed on Silica Gel as a Reusable Heterogeneous Dual-Purpose Catalyst for Conversion of Aldehydes/Ketones into Acetals/Ketals and Back Again Synthesis. 2008: 1249-1256. DOI: 10.1055/S-2008-1042940 |
0.653 |
|
| 2008 |
Chakraborti AK, Roy SR, Kumar D, Chopra P. Catalytic application of room temperature ionic liquids: [bmim][MeSO 4] as a recyclable catalyst for synthesis of bis(indolyl)methanes. Ion-fishing by MALDI-TOF-TOF MS and MS/MS studies to probe the proposed mechanistic model of catalysis Green Chemistry. 10: 1111-1118. DOI: 10.1039/B807572G |
0.704 |
|
| 2007 |
Barange DK, Nishad TC, Swamy NK, Bandameedi V, Kumar D, Sreekanth BR, Vyas K, Pal M. A remarkable accelerating effect of Ag-salt on intramolecular cyclization of o-(1-alkynyl)benzenesulfonamides. The Journal of Organic Chemistry. 72: 8547-50. PMID 17910502 DOI: 10.1021/Jo701470H |
0.396 |
|
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