Year |
Citation |
Score |
2020 |
Kaur S, Kumar A, Thakur S, Kumar K, Sharma R, Sharma A, Singh P, Sharma U, Kumar S, Landi M, Brestič M, Kaur S. Antioxidant, Antiproliferative and Apoptosis-Inducing Efficacy of Fractions from L. Leaves. Antioxidants (Basel, Switzerland). 9. PMID 32093300 DOI: 10.3390/Antiox9020173 |
0.519 |
|
2019 |
Kumar R, Sharma R, Kumar R, Sharma U. Cp*Rh(III)-Catalyzed Regioselective C(sp)-H Methylation of 8-Methylquinolines with Organoborons. Organic Letters. PMID 31859519 DOI: 10.1021/Acs.Orglett.9B04331 |
0.746 |
|
2019 |
Dhiman AK, Gupta SS, Sharma R, Kumar R, Sharma U. Rh(III)-Catalyzed C(8)-H Activation of Quinoline N-oxides: Regioselective C-Br and C-N Bond Formation. The Journal of Organic Chemistry. PMID 31257883 DOI: 10.1021/Acs.Joc.9B01538 |
0.802 |
|
2019 |
Sharma R, Kumar R, Sharma U. Rh/O2-Catalyzed C8 Olefination of Quinoline N-oxides with Activated and Unactivated Olefins. The Journal of Organic Chemistry. PMID 30693780 DOI: 10.1021/Acs.Joc.8B03176 |
0.698 |
|
2018 |
Kumar R, Sharma R, Kumar I, Upadhyay P, Dhiman AK, Kumar R, Kumar R, Purohit R, Sahal D, Sharma U. Evaluation of antiplasmodial potential of C-2 and C-8 modified quinolines: in vitro and in silico study. Medicinal Chemistry (Shariqah (United Arab Emirates)). PMID 30324888 DOI: 10.2174/1573406414666181015144413 |
0.711 |
|
2018 |
Sharma R, Kumar R, Kumar R, Upadhyay P, Sahal D, Sharma U. Rh(III)-catalyzed C(8)-H functionalization of quinolines via simultaneous C-C and C-O bond formation: Direct Synthesis of Quinoline Derivatives with Antiplasmodial Potential. The Journal of Organic Chemistry. PMID 30211555 DOI: 10.1021/Acs.Joc.8B02042 |
0.752 |
|
2018 |
Sharma R, Jandrotia R, Singh B, Sharma U, Kumar D. Comprehensive Metabolomics Study of Traditionally Important Rumex Species Found in Western Himalayan Region Natural Product Communications. 13. DOI: 10.1177/1934578X1801300219 |
0.584 |
|
2018 |
Sharma R, Sharma U. Remote C-H bond activation/transformations: A continuous growing synthetic tool; Part II Catalysis Reviews. 60: 497-565. DOI: 10.1080/01614940.2018.1474538 |
0.321 |
|
2018 |
Kumar I, Sharma R, Kumar R, Sharma U. C70 Fullerene‐Catalyzed Metal‐Free Photocatalytic ipso‐Hydroxylation of Aryl Boronic Acids: Synthesis of Phenols Advanced Synthesis & Catalysis. 360: 2013-2019. DOI: 10.1002/Adsc.201701573 |
0.779 |
|
2017 |
Sharma A, Sharma R, Arora R, Arora S, Singh B, Sharma U. Quantitative and Qualitative Analysis of Eruca sativa and Brassica juncea Seeds by UPLC-DAD and UPLC-ESI-QTOF Natural Product Communications. 12. DOI: 10.1177/1934578X1701200927 |
0.585 |
|
2017 |
Sharma R, Kumar I, Kumar R, Sharma U. Rhodium‐Catalyzed Remote C‐8 Alkylation of Quinolines with Activated and Unactivated Olefins: Mechanistic Study and Total Synthesis of EP4 Agonist Advanced Synthesis & Catalysis. 359: 3022-3028. DOI: 10.1002/Adsc.201700542 |
0.806 |
|
2016 |
Rattan R, Inder Fozdar B, Gautam V, Sharma R, Kumar D, Sharma U. Cuspidate A, new anti-fungal triterpenoid saponin from Lepidagathis cuspidata. Natural Product Research. 1-7. PMID 27827543 DOI: 10.1080/14786419.2016.1244192 |
0.51 |
|
2016 |
Arora R, Bhushan S, Kumar R, Mannan R, Kaur P, Singh B, Sharma R, Vig AP, Singh B, Singh AP, Arora S. To Analyze the Amelioration of Phenobarbital Induced Oxidative Stress by Erucin, as Indicated by Biochemical and Histological Alterations. Anti-Cancer Agents in Medicinal Chemistry. PMID 27087163 DOI: 10.2174/1871520616666160415154210 |
0.516 |
|
2016 |
Kumar R, Kumar I, Sharma R, Sharma U. Catalyst and solvent-free alkylation of quinoline N-oxides with olefins: A direct access to quinoline-substituted α-hydroxy carboxylic derivatives. Organic & Biomolecular Chemistry. PMID 26846299 DOI: 10.1039/C5Ob02600H |
0.765 |
|
2016 |
Kumar R, Kumar I, Sharma R, Sharma U. ChemInform Abstract: Catalyst and Solvent-Free Alkylation of Quinoline N-Oxides with Olefins: A Direct Access to Quinoline-Substituted α-Hydroxy Carboxylic Derivatives. Cheminform. 47. DOI: 10.1002/CHIN.201628177 |
0.728 |
|
2016 |
Sharma R, Kumar R, Kumar I, Sharma U. ChemInform Abstract: RhIII-Catalyzed Dehydrogenative Coupling of Quinoline N-Oxides with Alkenes: N-Oxide as Traceless Directing Group for Remote C-H Activation. Cheminform. 47. DOI: 10.1002/CHIN.201614150 |
0.765 |
|
2015 |
Rattan R, Reddy SG, Dolma SK, Fozdar BI, Gautam V, Sharma R, Sharma U. Triterpenoid Saponins from Clematis graveolens and Evaluation of their Insecticidal Activities. Natural Product Communications. 10: 1525-8. PMID 26594749 DOI: 10.1177/1934578X1501000909 |
0.507 |
|
2015 |
Sharma R, Thakur K, Kumar R, Kumar I, Sharma U. Distant C-H Activation/Functionalization: A New Horizon of Selectivity Beyond Proximity Catalysis Reviews - Science and Engineering. DOI: 10.1080/01614940.2015.1058623 |
0.772 |
|
2015 |
Sharma R, Bala M, Verma PK, Singh B. Water-Mediated Synthesis of Benzazole and Thiourea Motifs by Reacting Naturally Occurring Isothiocyanate with Amines Synthetic Communications. 45: 2106-2114. DOI: 10.1080/00397911.2015.1062514 |
0.546 |
|
2015 |
Sharma R, Kumar R, Kumar I, Singh B, Sharma U. Selective C-Si Bond Formation through C-H Functionalization Synthesis (Germany). 47: 2347-2366. DOI: 10.1055/S-0034-1380435 |
0.776 |
|
2015 |
Sharma R, Kumar R, Kumar I, Sharma U. RhIII-Catalyzed Dehydrogenative Coupling of Quinoline N-Oxides with Alkenes: N-Oxide as Traceless Directing Group for Remote C-H Activation European Journal of Organic Chemistry. 2015: 7519-7528. DOI: 10.1002/Ejoc.201501246 |
0.796 |
|
2015 |
Sharma R, Thakur K, Kumar R, Kumar I, Sharma U. ChemInform Abstract: Distant C-H Activation/Functionalization: A New Horizon of Selectivity Beyond Proximity Cheminform. 46: no-no. DOI: 10.1002/CHIN.201551225 |
0.756 |
|
2015 |
Sharma R, Kumar R, Kumar I, Singh B, Sharma U. ChemInform Abstract: Selective C-Si Bond Formation Through C-H Functionalization Cheminform. 46: no-no. DOI: 10.1002/CHIN.201541252 |
0.783 |
|
2014 |
Thakur K, Sharma R, Sharma U. Olefins as Unprecedented Feedstock for the Synthesis of Valuable Heterocycles: Regioselectivity Remains an Issue Synlett. 26: 137-141. DOI: 10.1055/S-0034-1379707 |
0.562 |
|
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