| Year |
Citation |
Score |
| 2024 |
Kumar R, Dutt S, Banerjee P. Electrochemical oxidative C-C bond cleavage of methylenecyclopropanes with alcohols. Chemical Communications (Cambridge, England). PMID 38530248 DOI: 10.1039/d4cc00843j |
0.355 |
|
| 2024 |
Kumar N, Sharma N, Kumar V, Kumar V, Jangid K, Devi B, Dwivedi AR, Giri K, Kumar R, Kumar V. Iodine-PEG as a unique combination for the metal-free synthesis of flavonoids through iodonium-triiodide ion-pair complexation. Rsc Advances. 14: 6225-6233. PMID 38375003 DOI: 10.1039/d3ra08810c |
0.303 |
|
| 2023 |
Kumar R, Ahsan F, Awasthi A, Swart M, Draksharapu A. Generation of Ru(III)-hypochlorite with resemblance to the heme-dependent haloperoxidase enzyme. Dalton Transactions (Cambridge, England : 2003). PMID 37609762 DOI: 10.1039/d3dt02028b |
0.307 |
|
| 2023 |
Kumar R, Banerjee N, Kumar P, Banerjee P. Electrochemical Synthesis and Reactivity of Three-membered Strained Carbo- and Heterocycles. Chemistry (Weinheim An Der Bergstrasse, Germany). e202301594. PMID 37436418 DOI: 10.1002/chem.202301594 |
0.331 |
|
| 2022 |
Kumar R, Taily IM, Banerjee P. Electrochemical sulfinylation of phenols with sulfides: a metal- and oxidant-free cross-coupling for the synthesis of aromatic sulfoxides. Chemical Communications (Cambridge, England). PMID 36507914 DOI: 10.1039/d2cc05207e |
0.365 |
|
| 2022 |
Kumar R, Chmielewski P, Lis T, Volkmer D, Stępień M. Tridecacyclene Tetraimide: An Easily Reduced Cyclooctatetraene Derivative. Angewandte Chemie (International Ed. in English). PMID 35819871 DOI: 10.1002/anie.202207486 |
0.573 |
|
| 2022 |
Rathore S, Mukhia S, Kapoor S, Bhatt V, Kumar R, Kumar R. Seasonal variability in essential oil composition and biological activity of Rosmarinus officinalis L. accessions in the western Himalaya. Scientific Reports. 12: 3305. PMID 35228638 DOI: 10.1038/s41598-022-07298-x |
0.656 |
|
| 2021 |
Anmol, Kumari S, Kumar R, Singh R, Aggarwal G, Agrawal P, Sahal D, Sharma U. Antiplasmodial diterpenoid alkaloid from Aconitum heterophyllum Wall. ex Royle: Isolation, characterization, and UHPLC-DAD based quantification. Journal of Ethnopharmacology. 114931. PMID 34942322 DOI: 10.1016/j.jep.2021.114931 |
0.74 |
|
| 2021 |
Gupta SS, Manisha, Kumar R, Dhiman AK, Sharma U. Predictable site-selective functionalization: Promoter group assisted -halogenation of -substituted heteroaromatics under metal-free condition. Organic & Biomolecular Chemistry. PMID 34730171 DOI: 10.1039/d1ob02000e |
0.832 |
|
| 2021 |
Kumar I, Kumar R, Gupta SS, Sharma U. C Fullerene Catalyzed Photoinduced Aerobic Oxidation of Benzylamines to Imines and Aldehydes. The Journal of Organic Chemistry. PMID 33886326 DOI: 10.1021/acs.joc.1c00297 |
0.823 |
|
| 2021 |
Thakur A, Dhiman AK, Sumit, Kumar R, Sharma U. Rh(III)-Catalyzed Regioselective C8-Alkylation of Quinoline -Oxides with Maleimides and Acrylates. The Journal of Organic Chemistry. PMID 33881315 DOI: 10.1021/acs.joc.1c00393 |
0.831 |
|
| 2020 |
Parmar D, Kumar R, Kumar R, Sharma U. Ru(II)-Catalyzed Chemoselective C(sp3)-H Monoarylation of 8-Methyl Quinolines with Arylboronic Acids. The Journal of Organic Chemistry. PMID 32812432 DOI: 10.1021/Acs.Joc.0C01603 |
0.799 |
|
| 2020 |
Dhiman AK, Thakur A, Kumar I, Kumar R, Sharma U. Co(III)-Catalyzed C-H Amidation of Nitrogen Containing Heterocycles with Dioxazolones under Mild Condition. The Journal of Organic Chemistry. PMID 32558566 DOI: 10.1021/Acs.Joc.0C01237 |
0.821 |
|
| 2020 |
Gupta SS, Kumar R, Sharma U. Regioselective Arylation of Quinoline -Oxides (C8), Indolines (C7) and --Butylbenzamide with Arylboronic Acids. Acs Omega. 5: 904-913. PMID 31956844 DOI: 10.1021/acsomega.9b03884 |
0.758 |
|
| 2020 |
Kumar R, Parmar D, Gupta SS, Chandra D, Dhiman AK, Sharma U. Cp*Rh(III)-Catalyzed Sterically Controlled C(sp3)-H Selective Mono- and Diarylation of 8-Methylquinolines with Organoborons. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31943447 DOI: 10.1002/Chem.201905591 |
0.792 |
|
| 2020 |
Walia S, Mukhia S, Bhatt V, Kumar R, Kumar R. Variability in chemical composition and antimicrobial activity of Tagetes minuta L. essential oil collected from different locations of Himalaya Industrial Crops and Products. 150: 112449. DOI: 10.1016/J.Indcrop.2020.112449 |
0.685 |
|
| 2020 |
Dhiman AK, Thakur A, Kumar R, Sharma U. Recent Advances in Rhodium‐Catalyzed Selective C‐H Bond Functionalization of Quinolines Asian Journal of Organic Chemistry. DOI: 10.1002/Ajoc.202000341 |
0.761 |
|
| 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 |
0.802 |
|
| 2019 |
Kumar R, Kumar R, Parmar D, Gupta SS, Sharma U. Ru(II)/ Rh(III)-Catalyzed C(sp3)-C(sp3) Bond Formation through C(sp3)-H Activation: Selective Linear Alkylation of 8-Methylquinolines and Ketoximes with Olefins. The Journal of Organic Chemistry. PMID 31842545 DOI: 10.1021/Acs.Joc.9B03257 |
0.837 |
|
| 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 |
0.827 |
|
| 2019 |
Dhiman AK, Chandra D, Kumar R, Sharma U. Catalyst-Free Synthesis of 2-Anilinoquinolines and 3-Hydroxyquinolines via Three-Component Reaction of Quinoline N-oxides, Aryldiazonium salts and Acetonitrile. The Journal of Organic Chemistry. PMID 31070920 DOI: 10.1021/Acs.Joc.9B00739 |
0.797 |
|
| 2019 |
Thakur M, Bhatt V, Kumar R. Effect of shade level and mulch type on growth, yield and essential oil composition of damask rose (Rosa damascena Mill.) under mid hill conditions of Western Himalayas. Plos One. 14: e0214672. PMID 30946775 DOI: 10.1371/Journal.Pone.0214672 |
0.67 |
|
| 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 |
0.769 |
|
| 2019 |
Kumar R, Kumar R, Chandra D, Sharma U. Cp*CoIII-Catalyzed Alkylation of Primary and Secondary C(sp3)-H Bonds of 8-Alkylquinolines with Maleimides. The Journal of Organic Chemistry. PMID 30620183 DOI: 10.1021/Acs.Joc.8B02974 |
0.81 |
|
| 2019 |
Chandra D, Dhiman AK, Kumar R, Sharma U. Microwave‐Assisted Metal‐Free Rapid Synthesis of C4‐Arylated Quinolines via Povarov Type Multicomponent Reaction European Journal of Organic Chemistry. 2019: 2753-2758. DOI: 10.1002/Ejoc.201900325 |
0.782 |
|
| 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 |
0.753 |
|
| 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 |
0.798 |
|
| 2018 |
Kumar R, Chaudhary S, Kumar R, Upadhyay P, Sahal D, Sharma U. A Catalyst and Additive-free Diastereoselective 1,3-Dipolar Cycloaddition of Quinolinium Imides with Olefins, Maleimides and Benzynes: Direct Access to Fused N,N´-Heterocycles with Promising Activity against Drug Resistant Malaria Parasite. The Journal of Organic Chemistry. PMID 30160960 DOI: 10.1021/Acs.Joc.8B01520 |
0.707 |
|
| 2018 |
Kumar R, Sharma R, Patil RD, Mal G, Kumar A, Patial V, Kumar P, Singh B. Sub-chronic toxicopathological study of lantadenes of Lantana camara weed in Guinea pigs. Bmc Veterinary Research. 14: 129. PMID 29653586 DOI: 10.1186/S12917-018-1444-X |
0.426 |
|
| 2018 |
Kaundal M, Bhatt V, Kumar R. Elevated CO2 and Temperature Effect on Essential Oil Content and Composition of Valeriana jatamansi Jones. with Organic Manure Application in a Western Himalayan Region Journal of Essential Oil Bearing Plants. 21: 1041-1050. DOI: 10.1080/0972060X.2018.1497547 |
0.67 |
|
| 2018 |
Kumar I, Kumar R, Sharma U. Recent Advances in the Regioselective Synthesis of Indoles via C–H Activation/Functionalization Synthesis. 50: 2655-2677. DOI: 10.1055/S-0037-1609733 |
0.801 |
|
| 2017 |
Dhiman AK, Kumar R, Kumar R, Sharma U. Metal-free synthesis of 2-substituted-3-(2-hydroxyaryl)quinolines and 4-(2-hydroxyaryl)acridines via benzyne chemistry. The Journal of Organic Chemistry. PMID 29111735 DOI: 10.1021/Acs.Joc.7B02149 |
0.782 |
|
| 2017 |
Kumar R, Dhiman AK, Sharma U. Regioselective Metal‐Free C2−H Arylation of Quinoline N‐Oxides with Aryldiazonium Salts/Anilines under Ambient Conditions Asian Journal of Organic Chemistry. 6: 1043-1053. DOI: 10.1002/Ajoc.201700267 |
0.82 |
|
| 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 |
0.847 |
|
| 2016 |
Kumari K, Jain D, Kumar R, Mohan A, Kumar R. Metastatic carotid body paraganglioma of lungs and lymph nodes: Unsuspected diagnosis on EBUS-TBNA. Diagnostic Cytopathology. PMID 27902883 DOI: 10.1002/dc.23650 |
0.347 |
|
| 2016 |
Arora R, Kumar R, Mahajan J, Vig AP, Singh B, Singh B, Arora S. 3-Butenyl isothiocyanate: a hydrolytic product of glucosinolate as a potential cytotoxic agent against human cancer cell lines. Journal of Food Science and Technology. 53: 3437-3445. PMID 27777449 DOI: 10.1007/S13197-016-2316-7 |
0.41 |
|
| 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 |
0.652 |
|
| 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 |
0.814 |
|
| 2016 |
Kumar D, Kumar R, Singh B, Ahuja PS. Comprehensive chemical profiling of Picrorhiza kurroa Royle ex Benth using NMR, HPTLC and LC-MS/MS techniques. Combinatorial Chemistry & High Throughput Screening. PMID 26777484 DOI: 10.2174/1386207319666160114092538 |
0.418 |
|
| 2016 |
Kumar R, Gleißner EH, Tiu EG, Yamakoshi Y. C70 as a Photocatalyst for Oxidation of Secondary Benzylamines to Imines. Organic Letters. 18: 184-7. PMID 26700114 DOI: 10.1021/Acs.Orglett.5B03194 |
0.336 |
|
| 2015 |
Sharma S, Walia S, Singh B, Kumar R. Comprehensive Review on Agro technologies of Low Calorie Natural Sweetener Stevia (Stevia rebaudiana Bertoni): A boon to diabetic. Journal of the Science of Food and Agriculture. PMID 26467712 DOI: 10.1002/Jsfa.7500 |
0.508 |
|
| 2015 |
Kumar R, Singh G, Todaro LJ, Yang L, Zajc B. E- or Z-Selective synthesis of 4-fluorovinyl-1,2,3-triazoles with fluorinated second-generation Julia-Kocienski reagents. Organic & Biomolecular Chemistry. 13: 1536-49. PMID 25491086 DOI: 10.1039/C4Ob02179G |
0.325 |
|
| 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 |
0.796 |
|
| 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 |
0.84 |
|
| 2014 |
Arora R, Bhushan S, Kumar R, Mannan R, Kaur P, Singh AP, Singh B, Vig AP, Sharma D, Arora S. Hepatic dysfunction induced by 7, 12-dimethylbenz(α)anthracene and its obviation with erucin using enzymatic and histological changes as indicators. Plos One. 9: e112614. PMID 25390337 DOI: 10.1371/Journal.Pone.0112614 |
0.43 |
|
| 2014 |
Arora R, Sharma D, Kumar R, Singh B, Vig AP, Arora S. Evaluating extraction conditions of glucosinolate hydrolytic products from seeds of Eruca sativa (Mill.) Thell. using GC-MS. Journal of Food Science. 79: C1964-9. PMID 25252034 DOI: 10.1111/1750-3841.12579 |
0.453 |
|
| 2014 |
Sood A, Sharma V, Chaudhry A, Kumar R, Arora S, Rajnikant, Gupta V, Ishar MPS. Synthesis and evaluation of 3-salicyloylpyridine derivatives as cytotoxic mitochondrial apoptosis inducers Bioorganic and Medicinal Chemistry Letters. 24: 4724-4728. PMID 25176329 DOI: 10.1016/j.bmcl.2014.08.010 |
0.744 |
|
| 2014 |
Kumar R, Sharma S, Sood S, Agnihotri VK, Singh V, Singh B. Evaluation of several Rosa damascena varieties and Rosa bourboniana accession for essential oil content and composition in western Himalayas Journal of Essential Oil Research. 26: 147-152. DOI: 10.1080/10412905.2013.829004 |
0.473 |
|
| 2013 |
Singh G, Kumar R, Swett J, Zajc B. Modular synthesis of N-vinyl benzotriazoles. Organic Letters. 15: 4086-9. PMID 23915255 DOI: 10.1021/ol401661j |
0.333 |
|
| 2013 |
Kumar R, Sharma S, Ramesh K, Singh B. Effects of shade regimes and planting geometry on growth, yield and quality of the natural sweetener plant stevia (Stevia rebaudiana Bertoni) in north-western Himalaya Archives of Agronomy and Soil Science. 59: 963-979. DOI: 10.1080/03650340.2012.699676 |
0.481 |
|
| 2013 |
Kumar R, Sharma S, Sood S, Agnihotri VK, Singh B. Effect of diurnal variability and storage conditions on essential oil content and quality of damask rose (Rosa damascena Mill.) flowers in north western Himalayas Scientia Horticulturae. 154: 102-108. DOI: 10.1016/J.Scienta.2013.02.002 |
0.474 |
|
| 2012 |
Kumar R, Zajc B. Stereoselective synthesis of conjugated fluoro enynes. The Journal of Organic Chemistry. 77: 8417-27. PMID 23005035 DOI: 10.1021/jo300971w |
0.324 |
|
| 2012 |
Sharma UK, Sharma N, Salwan R, Kumar R, Kasana RC, Sinha AK. Efficient synthesis of hydroxystyrenes via biocatalytic decarboxylation/deacetylation of substituted cinnamic acids by newly isolated Pantoea agglomerans strains. Journal of the Science of Food and Agriculture. 92: 610-7. PMID 21919002 DOI: 10.1002/Jsfa.4616 |
0.568 |
|
| 2012 |
Kumar R, Bhandari P, Singh B, Ahuja PS. Evaluation of Picrorhiza kurrooa accessions for growth and quality in north western Himalayas Journal of Medicinal Plants Research. 6: 2660-2665. DOI: 10.5897/Jmpr11.1618 |
0.489 |
|
| 2012 |
Kumar R, Ramesh K, Pathania V, Singh B. Effect of Transplanting Date on Growth, Yield and Oil Quality of Tagetes minuta L. in Mid Hill of North -Western Himalaya Journal of Essential Oil Bearing Plants. 15: 405-414. DOI: 10.1080/0972060X.2012.10644068 |
0.469 |
|
| 2011 |
Sharma N, Sharma A, Shard A, Kumar R, Saima, Sinha AK. Pd-catalyzed orthogonal Knoevenagel/Perkin condensation-decarboxylation-Heck/Suzuki sequences: tandem transformations of benzaldehydes into hydroxy-functionalized antidiabetic stilbene-cinnamoyl hybrids and asymmetric distyrylbenzenes. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 10350-6. PMID 21812043 DOI: 10.1002/Chem.201101174 |
0.354 |
|
| 2011 |
Sharma A, Sharma N, Shard A, Kumar R, Mohanakrishnan D, Saima, Sinha AK, Sahal D. Tandem allylic oxidation-condensation/esterification catalyzed by silica gel: an expeditious approach towards antimalarial diaryldienones and enones from natural methoxylated phenylpropenes. Organic & Biomolecular Chemistry. 9: 5211-9. PMID 21625717 DOI: 10.1039/C1Ob05293D |
0.345 |
|
| 2011 |
Kumar R, Sharma N, Sharma N, Sharma A, Sinha AK. Metal-free activation of H₂O₂ by synergic effect of ionic liquid and microwave: chemoselective oxidation of benzylic alcohols to carbonyls and unexpected formation of anthraquinone in aqueous condition. Molecular Diversity. 15: 687-95. PMID 21113797 DOI: 10.1007/S11030-010-9292-Z |
0.327 |
|
| 2011 |
Kumar R, Sharma S, Singh B. Evaluation of Transplanting Time Effect on Characteristic Growth, Essential Oil and its Composition in Clary Sage (Salvia sclarea L.) in North-Western Himalayas Journal of Essential Oil Bearing Plants. 14: 260-265. DOI: 10.1080/0972060X.2011.10643931 |
0.47 |
|
| 2011 |
Sharma N, Sharma UK, Kumar R, Katoch N, Kumar R, Sinha AK. First Bovine Serum Albumin-Promoted Synthesis of Enones, Cinnamic Acids and Coumarins in Ionic Liquid: An Insight into the Role of Protein Impurities in Porcine Pancreas Lipase for Olefinic Bond Formation Advanced Synthesis & Catalysis. 353: 871-878. DOI: 10.1002/Adsc.201000870 |
0.621 |
|
| 2010 |
Zajc B, Kumar R. Synthesis of Fluoroolefins via Julia-Kocienski Olefination Synthesis. 2010: 1822-1836. PMID 22544979 DOI: 10.1055/S-0029-1218789 |
0.341 |
|
| 2010 |
Sharma A, Sharma N, Kumar R, Shard A, Sinha AK. Direct olefination of benzaldehydes into hydroxy functionalized oligo (p-phenylenevinylene)s via Pd-catalyzed heterodomino Knoevenagel-decarboxylation-Heck sequence and its application for fluoride sensing pi-conjugated units. Chemical Communications (Cambridge, England). 46: 3283-5. PMID 20442887 DOI: 10.1039/C001980A |
0.315 |
|
| 2009 |
Sharma UK, Sharma N, Kumar R, Kumar R, Sinha AK. Biocatalytic promiscuity of lipase in chemoselective oxidation of aryl alcohols/acetates: a unique synergism of CAL-B and [hmim]Br for the metal-free H2O2 activation. Organic Letters. 11: 4846-8. PMID 19788267 DOI: 10.1021/Ol901917E |
0.53 |
|
| 2009 |
Sharma A, Sharma N, Kumar R, Sharma UK, Sinha AK. Water-promoted cascade synthesis of alpha-arylaldehydes from arylalkenes using N-halosuccinimides: an avenue for asymmetric oxidation using Cinchona organocatalysis. Chemical Communications (Cambridge, England). 5299-301. PMID 19707652 DOI: 10.1039/B908717F |
0.568 |
|
| 2008 |
Sharma A, Kumar R, Sharma N, Kumar V, Sinha AK. Unique Versatility of Ionic Liquids as Clean Decarboxylation Catalyst Cum Solvent: A Metal‐ and Quinoline‐Free Paradigm towards Synthesis of Indoles, Styrenes, Stilbenes and Arene Derivatives under Microwave Irradiation in Aqueous Conditions Advanced Synthesis & Catalysis. 350: 2910-2920. DOI: 10.1002/Adsc.200800537 |
0.386 |
|
| 2007 |
Kumar R, Mittal A, Ramachandran U. Design and synthesis of 6-methyl-2-oxo-1,2,3,4-tetrahydro-pyrimidine-5-carboxylic acid derivatives as PPARγ activators Bioorganic and Medicinal Chemistry Letters. 17: 4613-4618. PMID 17574414 DOI: 10.1016/J.Bmcl.2007.05.081 |
0.308 |
|
| 1994 |
Kumar R, Wiebe LI, Knaus EE. A mild and efficient methodology for the synthesis of 5-halogeno uracil nucleosides that occurs via a 5-halogeno-6-azido-5,6-dihydro intermediate Canadian Journal of Chemistry. 72: 2005-2010. DOI: 10.1139/V94-256 |
0.306 |
|
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