Year |
Citation |
Score |
2023 |
Parvin T. Multicomponent Reactions Using C,N-Binucleophilic Nature of Aminopyrazoles: Construction of Pyrazole-Fused Heterocycles. Topics in Current Chemistry (Cham). 381: 19. PMID 37237061 DOI: 10.1007/s41061-023-00427-8 |
0.519 |
|
2023 |
Parvin T. Domino Reaction for the Synthesis of Pyrazole/Isoxazole Fused Naphthyridine Derivatives Involving Indole Ring Opening and Double Ring Formation. The Journal of Organic Chemistry. PMID 37159509 DOI: 10.1021/acs.joc.3c00135 |
0.532 |
|
2022 |
Bhaumick P, Kumar R, Acharya SS, Parvin T, Choudhury LH. Multicomponent Synthesis of Fluorescent Thiazole-Indole Hybrids and Thiazole-Based Novel Polymers. The Journal of Organic Chemistry. 87: 11399-11413. PMID 35998330 DOI: 10.1021/acs.joc.2c00922 |
0.801 |
|
2022 |
Parvin T. One-pot multicomponent synthesis of benzophenazine tethered tetrahydropyridopyrimidine derivatives. Molecular Diversity. PMID 35460459 DOI: 10.1007/s11030-022-10426-4 |
0.456 |
|
2022 |
Ali D, Parvin T, Choudhury LH. Visible Light-Mediated C(sp)-H Selenylation of Amino Pyrazole and Amino Uracils in the Presence of Rose Bengal as an Organophotocatalyst. The Journal of Organic Chemistry. PMID 34994553 DOI: 10.1021/acs.joc.1c02565 |
0.807 |
|
2021 |
Yadav R, Parvin T, Panday AK, Choudhury LH. Synthesis of styryl-linked fused dihydropyridines by catalyst-free multicomponent reactions. Molecular Diversity. PMID 33860877 DOI: 10.1007/s11030-021-10216-4 |
0.829 |
|
2020 |
Parvin T, Yadav R, Choudhury LH. Recent applications of thiourea-based organocatalysts in asymmetric multicomponent reactions (AMCRs). Organic & Biomolecular Chemistry. PMID 32644077 DOI: 10.1039/D0Ob00595A |
0.826 |
|
2020 |
Mahata A, Bhaumick P, Panday AK, Yadav R, Parvin T, Choudhury LH. Multicomponent synthesis of diphenyl-1,3-thiazole-barbituric acid hybrids and their fluorescence property studies New Journal of Chemistry. 44: 4798-4811. DOI: 10.1039/D0Nj00406E |
0.62 |
|
2019 |
Kumari P, Yadav R, Bharti R, Parvin T. Regioselective synthesis of pyrimidine-fused tetrahydropyridines and pyridines by microwave-assisted one-pot reaction. Molecular Diversity. PMID 30843127 DOI: 10.1007/S11030-019-09929-4 |
0.83 |
|
2018 |
Kumari P, Bharti R, Parvin T. Synthesis of aminouracil-tethered tri-substituted methanes in water by iodine-catalyzed multicomponent reactions. Molecular Diversity. PMID 30109557 DOI: 10.1007/S11030-018-9862-Z |
0.834 |
|
2018 |
Panday AK, Mishra R, Jana A, Parvin T, Choudhury LH. Synthesis of Pyrimidine Fused Quinolines by Ligand-Free Copper-Catalyzed Domino Reactions. The Journal of Organic Chemistry. PMID 29570285 DOI: 10.1021/Acs.Joc.7B03272 |
0.818 |
|
2018 |
Bharti R, Kumari P, Parvin T, Choudhury LH. Recent Advances of Aminopyrimidines in Multicomponent Reactions Current Organic Chemistry. 22: 417-445. DOI: 10.2174/1385272822666171212152406 |
0.793 |
|
2017 |
Bharti R, Kumari P, Parvin T, Choudhury LH. Molecular diversity from the three-component reaction of 2-hydroxy-1,4-naphthaquinone, aldehydes and 6-aminouracils: a reaction condition dependent MCR Rsc Advances. 7: 3928-3933. DOI: 10.1039/C6Ra18828A |
0.799 |
|
2017 |
Jana A, Panday AK, Mishra R, Parvin T, Choudhury LH. Synthesis of Thio and Selenoethers of Cyclic β-Hydroxy Carbonyls and Amino Uracils: A Metal-Free Regioselective I2
/DMSO Mediated Reaction Chemistryselect. 2: 9420-9424. DOI: 10.1002/SLCT.201702066 |
0.448 |
|
2016 |
Bharti R, Parvin T. Multicomponent synthesis of diverse pyrano-fused benzophenazines using bifunctional thiourea-based organocatalyst in aqueous medium. Molecular Diversity. 20: 867-876. PMID 27317166 DOI: 10.1007/S11030-016-9681-Z |
0.754 |
|
2016 |
Bharti R, Parvin T. ChemInform Abstract: One-Pot Synthesis of Highly Functionalized Tetrahydropyridines: A Camphoresulfonic Acid Catalyzed Multicomponent Reaction. Cheminform. 47: no-no. DOI: 10.1002/CHIN.201610165 |
0.743 |
|
2015 |
Bharti R, Parvin T. Molecular Diversity from the L-Proline-Catalyzed, Three-Component Reactions of 4-Hydroxycoumarin, Aldehyde, and 3-Aminopyrazole or 1,3-Dimethyl-6-aminouracil Synthetic Communications. 45: 1442-1450. DOI: 10.1080/00397911.2015.1023900 |
0.707 |
|
2015 |
Bharti R, Parvin T. Diversity oriented synthesis of tri-substituted methane containing aminouracil and hydroxynaphthoquinone/hydroxycoumarin moiety using organocatalysed multicomponent reactions in aqueous medium Rsc Advances. 5: 66833-66839. DOI: 10.1039/C5Ra13093J |
0.787 |
|
2015 |
Bharti R, Parvin T. ChemInform Abstract: Molecular Diversity from the L-Proline-Catalyzed, Three-Component Reactions of 4-Hydroxycoumarin, Aldehyde, and 3-Aminopyrazole or 1,3-Dimethyl-6-aminouracil. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201537164 |
0.694 |
|
2014 |
Karamthulla S, Pal S, Parvin T, Choudhury LH. L-proline catalyzed multicomponent reactions: facile access to 2H-benzo[g]pyrazolo[3,4-b]quinoline-5,10(4H,11H)-dione derivatives Rsc Adv.. 4: 15319-15324. DOI: 10.1039/C4Ra00876F |
0.412 |
|
2014 |
Bharti R, Parvin T. One-pot Synthesis of Highly Functionalized Tetrahydropyridines: A Camphoresulfonic Acid Catalyzed Multicomponent Reaction Journal of Heterocyclic Chemistry. 52: 1806-1811. DOI: 10.1002/Jhet.2268 |
0.755 |
|
2013 |
Pal S, Choudhury LH, Parvin T. One-Pot Multicomponent Reactions for the Efficient Synthesis of Highly Functionalized Dihydropyridines Synthetic Communications. 43: 986-992. DOI: 10.1080/00397911.2011.618283 |
0.629 |
|
2013 |
Pal S, Choudhury LH, Parvin T. ChemInform Abstract: One-Pot Multicomponent Reactions for the Efficient Synthesis of Highly Functionalized Dihydropyridines. Cheminform. 44: no-no. DOI: 10.1002/CHIN.201329158 |
0.535 |
|
2012 |
Pal S, Choudhury LH, Parvin T. VCl3 catalyzed imine-based multicomponent reactions for the facile access of functionalized tetrahydropyridines and β-amino carbonyls. Molecular Diversity. 16: 129-43. PMID 22042610 DOI: 10.1007/S11030-011-9339-9 |
0.827 |
|
2012 |
Khan MN, Pal S, Parvin T, Choudhury LH. A simple and efficient method for the facile access of highly functionalized pyridines and their fluorescence property studies Rsc Advances. 2: 12305. DOI: 10.1039/C2Ra21385K |
0.548 |
|
2011 |
Choudhury LH, Parvin T. Recent advances in the chemistry of imine-based multicomponent reactions (MCRs). Tetrahedron. 67: 8213-8228. PMID 32287421 DOI: 10.1016/J.Tet.2011.07.020 |
0.808 |
|
2010 |
Choudhury LH, Parvin T, Khan AT. ChemInform Abstract: Recent Advances in the Application of Bromodimethylsulfonium Bromide (BDMS) in Organic Synthesis Cheminform. 41. DOI: 10.1002/CHIN.201005240 |
0.45 |
|
2009 |
Khan AT, Parvin T, Choudhury LH. A Simple and Convenient One-Pot Synthesis of Benzimidazole Derivatives Using Cobalt(II) Chloride Hexahydrate as Catalyst Synthetic Communications. 39: 2339-2346. DOI: 10.1080/00397910802654815 |
0.625 |
|
2009 |
Parvin T. Methyl Acetoacetate: A Useful Reagent in Multicomponent Reactions Synlett. 2009: 2713-2714. DOI: 10.1055/s-0029-1217967 |
0.412 |
|
2009 |
Choudhury LH, Parvin T, Khan AT. Recent advances in the application of bromodimethylsulfonium bromide (BDMS) in organic synthesis Tetrahedron. 65: 9513-9526. DOI: 10.1016/J.Tet.2009.07.052 |
0.508 |
|
2009 |
Khan AT, Parvin T, Choudhury LH. ChemInform Abstract: A Simple and Convenient One-Pot Synthesis of Benzimidazole Derivatives Using Cobalt(II) Chloride Hexahydrate as Catalyst. Cheminform. 40: no-no. DOI: 10.1002/CHIN.200951149 |
0.509 |
|
2008 |
Khan AT, Parvin T, Choudhury LH. Effects of substituents in the beta-position of 1,3-dicarbonyl compounds in bromodimethylsulfonium bromide-catalyzed multicomponent reactions: a facile access to functionalized piperidines. The Journal of Organic Chemistry. 73: 8398-402. PMID 18841917 DOI: 10.1021/Jo8014962 |
0.773 |
|
2008 |
Khan AT, Parvin T, Choudhury LH. Bromodimethylsulfonium Bromide Catalyzed Three-Component Mannich-Type Reactions European Journal of Organic Chemistry. 2008: 834-839. DOI: 10.1002/Ejoc.200700643 |
0.735 |
|
2008 |
Khan AT, Parvin T, Choudhury LH. ChemInform Abstract: Bromodimethylsulfonium Bromide Catalyzed Three-Component Mannich-Type Reactions. Cheminform. 39. DOI: 10.1002/CHIN.200825101 |
0.635 |
|
2007 |
Khan AT, Parvin T, Gazi S, Choudhury LH. Bromodimethylsulfonium bromide mediated Michael addition of amines to electron deficient alkenes Tetrahedron Letters. 48: 3805-3808. DOI: 10.1016/J.Tetlet.2007.03.163 |
0.607 |
|
2007 |
Khan AT, Parvin T, Choudhury LH, Ghosh S. A simple synthetic protocol for oxidation of alkyl-arenes into ketones using a combination of HBr–H2O2 Tetrahedron Letters. 48: 2271-2274. DOI: 10.1016/J.Tetlet.2007.01.172 |
0.598 |
|
2007 |
Khan AT, Parvin T, Choudhury LH. Iron(III) chloride-catalyzed convenient one-pot synthesis of β-acetamido carbonyl compounds Tetrahedron. 63: 5593-5601. DOI: 10.1016/J.TET.2007.04.019 |
0.463 |
|
2007 |
Khan AT, Parvin T, Choudhury LH. Iron(III) Chloride-Catalyzed Convenient One-Pot Synthesis of β-Acetamido Carbonyl Compounds. Cheminform. 38. DOI: 10.1016/J.Tet.2007.04.019 |
0.721 |
|
2007 |
Khan AT, Parvin T, Gazi S, Choudhury LH. Bromodimethylsulfonium Bromide Mediated Michael Addition of Amines to Electron Deficient Alkenes. Cheminform. 38. DOI: 10.1002/CHIN.200737049 |
0.417 |
|
2007 |
Khan AT, Parvin T, Choudhury LH, Ghosh S. A Simple Synthetic Protocol for Oxidation of Alkyl-Arenes into Ketones Using a Combination of HBr—H2O2. Cheminform. 38. DOI: 10.1002/CHIN.200728084 |
0.452 |
|
2007 |
Khan AT, Choudhury LH, Parvin T, Ali MA. CeCl3×7H2O: An Efficient and Reusable Catalyst for the Preparation of β-Acetamido Carbonyl Compounds by Multi-Component Reactions (MCRs). Cheminform. 38. DOI: 10.1002/CHIN.200708059 |
0.604 |
|
2006 |
Khan A, Parvin T, Choudhury L. Silica-Supported Perchloric Acid (HClO4-SiO2): A Versatile Catalyst for Tetrahydropyranylation, Oxathioacetalization and Thioacetalization Synthesis. 2006: 2497-2502. DOI: 10.1055/S-2006-942465 |
0.628 |
|
2006 |
Khan AT, Choudhury LH, Parvin T, Ali MA. CeCl3·7H2O: an efficient and reusable catalyst for the preparation of β-acetamido carbonyl compounds by multi-component reactions (MCRs) Tetrahedron Letters. 47: 8137-8141. DOI: 10.1016/J.Tetlet.2006.09.041 |
0.642 |
|
2006 |
Khan AT, Parvin T, Choudhury LH. Silica-Supported Perchloric Acid (HClO4—SiO2): A Versatile Catalyst for Tetrahydropyranylation, Oxathioacetalization and Thioacetalization. Cheminform. 37. DOI: 10.1002/CHIN.200650066 |
0.439 |
|
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