| Year |
Citation |
Score |
| 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 |
0.715 |
|
| 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 |
0.74 |
|
| 2014 |
Shah P, Dhameliya TM, Bansal R, Nautiyal M, Kommi DN, Jadhavar PS, Sridevi JP, Yogeeswari P, Sriram D, Chakraborti AK. N-Arylalkylbenzo[d]thiazole-2-carboxamides as anti-mycobacterial agents: Design, new methods of synthesis and biological evaluation Medchemcomm. 5: 1489-1495. DOI: 10.1039/C4Md00224E |
0.717 |
|
| 2014 |
Seth K, Roy SR, Kommi DN, Pipaliya BV, Chakraborti AK. Silver nanoparticle-catalysed phenolysis of epoxides under neutral conditions: Scope and limitations of metal nanoparticles and applications towards drug synthesis Journal of Molecular Catalysis a: Chemical. 392: 164-172. DOI: 10.1016/J.Molcata.2014.05.011 |
0.721 |
|
| 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 |
0.791 |
|
| 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 |
0.787 |
|
| 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 |
0.804 |
|
| 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 |
0.708 |
|
| 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 |
0.75 |
|
| 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 |
0.587 |
|
| 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 |
0.791 |
|
| 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 |
0.764 |
|
| 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 |
0.566 |
|
| 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 |
0.769 |
|
| 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 |
0.79 |
|
| 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 |
0.638 |
|
| 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 |
0.62 |
|
| 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 |
0.624 |
|
| 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 |
0.629 |
|
| 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 |
0.572 |
|
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