| Year |
Citation |
Score |
| 2024 |
Sarkar S, Pal S, Santra S, Zyryanov GV, Majee A. Visible-Light-Triggered Synthesis of -α-Ketoacylated Sulfoximines by Denitrogenative and Oxidative Functionalization of Vinyl Azides. The Journal of Organic Chemistry. PMID 38757898 DOI: 10.1021/acs.joc.4c00796 |
0.313 |
|
| 2024 |
Sarkar S, Pal S, Mukherjee A, Santra S, Zyryanov GV, Majee A. Visible-Light-Promoted Metal- and Photocatalyst-Free Reactions between Arylglyoxylic Acids and Tetraalkylthiuram Disulfides: Synthesis of α-Ketoamides. The Journal of Organic Chemistry. 89: 1473-1482. PMID 38225732 DOI: 10.1021/acs.joc.3c02081 |
0.415 |
|
| 2023 |
Zyryanov GV, Kopchuk DS, Kovalev IS, Santra S, Majee A, Ranu BC. Pillararenes as Promising Carriers for Drug Delivery. International Journal of Molecular Sciences. 24. PMID 36982244 DOI: 10.3390/ijms24065167 |
0.354 |
|
| 2022 |
Samanta S, Chatterjee R, Sarkar S, Pal S, Mukherjee A, Butorin II, Konovalova OA, Choudhuri T, Chakraborty K, Santra S, Zyryanov GV, Majee A. Brønsted acidic ionic liquid-catalyzed tandem reaction: an efficient and sustainable approach towards the regioselective synthesis and molecular docking studies of 4-hydroxycoumarin-substituted indoles bearing lower -factors. Organic & Biomolecular Chemistry. PMID 36346273 DOI: 10.1039/d2ob01431a |
0.798 |
|
| 2021 |
Das S, Chatterjee S, Mondal S, Modak A, Chandra BK, Das S, Nessim GD, Majee A, Bhaumik A. Correction: Thiadiazole containing N- and S-rich highly ordered periodic mesoporous organosilica for efficient removal of Hg(II) from polluted water. Chemical Communications (Cambridge, England). PMID 34723298 DOI: 10.1039/d1cc90375f |
0.756 |
|
| 2021 |
De A, Santra S, Khalymbadzha IA, Zyryanov GV, Majee A. A practicable synthesis of 2,3-disubstituted 1,4-dioxanes bearing a carbonyl functionality from α,β-unsaturated ketones using the Williamson strategy. Organic & Biomolecular Chemistry. PMID 33506239 DOI: 10.1039/d0ob01448f |
0.4 |
|
| 2020 |
Rahman M, Bagdi AK, Kopchuk DS, Kovalev IS, Zyryanov GV, Chupakhin ON, Majee A, Hajra A. Recent advances in the synthesis of fluorinated compounds an aryne intermediate. Organic & Biomolecular Chemistry. PMID 33201968 DOI: 10.1039/d0ob01638a |
0.576 |
|
| 2020 |
De A, Santra S, Zyryanov GV, Majee A. Self-Catalyzed Rapid Synthesis of -Acylated/-Formylated α-Aminoketones and -Hydroxymethylated Formamides from 3-Aryl-2-Azirines and 2-Me/Ph-3-Aryl-2-Azirines. Organic Letters. PMID 32356998 DOI: 10.1021/Acs.Orglett.0C01206 |
0.426 |
|
| 2020 |
Das S, Chatterjee S, Mondal S, Modak A, Chandra BK, Das S, Nessim GD, Majee A, Bhaumik A. Thiadiazole containing N- and S-rich highly ordered periodic mesoporous organosilica for efficient removal of Hg(ii) from polluted water. Chemical Communications (Cambridge, England). PMID 32149309 DOI: 10.1039/D0Cc00407C |
0.76 |
|
| 2020 |
Samanta S, Santra S, Chatterjee R, Majee A. A new tandem synthesis of bis(β,β'-dialkoxy carbonyl) compounds by oxidative cleavage of aziridines under metal-free conditions. Organic & Biomolecular Chemistry. PMID 31894233 DOI: 10.1039/C9Ob02451D |
0.782 |
|
| 2020 |
Egorov IN, Santra S, Kopchuk DS, Kovalev IS, Zyryanov GV, Majee A, Ranu BC, Rusinov VL, Chupakhin ON. Ball milling: an efficient and green approach for asymmetric organic syntheses Green Chemistry. 22: 302-315. DOI: 10.1039/C9Gc03414E |
0.538 |
|
| 2020 |
Samanta S, Mahato S, Chatterjee R, Santra S, Zyryanov GV, Majee A. Nano indium oxide-catalyzed domino reaction for the synthesis of N-alkoxylated benzimidazoles Tetrahedron Letters. 61: 152177. DOI: 10.1016/J.Tetlet.2020.152177 |
0.829 |
|
| 2020 |
De A, Santra S, Kovalev IS, Kopchuk DS, Zyryanov GV, Chupakhin ON, Charushin VN, Majee A. Synthesis of 2-imidazolines by co-grinding of N-tosylaziridines and nitriles Mendeleev Communications. 30: 188-189. DOI: 10.1016/J.Mencom.2020.03.019 |
0.424 |
|
| 2020 |
Das SK, Krishna Chandra B, Molla RA, Sengupta M, Islam SM, Majee A, Bhaumik A. CuO grafted triazine functionalized covalent organic framework as an efficient catalyst for C-C homo coupling reaction Molecular Catalysis. 480: 110650. DOI: 10.1016/J.Mcat.2019.110650 |
0.454 |
|
| 2020 |
Chatterjee R, Santra S, Zyryanov GV, Majee A. Brønsted acidic ionic liquid–catalyzed tandem trimerization of indoles: An efficient approach towards the synthesis of indole 3,3′‐trimers under solvent‐free conditions Journal of Heterocyclic Chemistry. 57: 1863-1874. DOI: 10.1002/Jhet.3914 |
0.755 |
|
| 2020 |
Egorov IN, Santra S, Kopchuk DS, Kovalev IS, Zyryanov GV, Majee A, Ranu BC, Rusinov VL, Chupakhin ON. Direct Asymmetric Arylation of Imines Advanced Synthesis & Catalysis. DOI: 10.1002/Adsc.202000548 |
0.591 |
|
| 2019 |
Das T, Chatterjee R, Majee A, Uyama H, Morgan D, Nandi M. In situ synthesis of CuO nanoparticles over functionalized mesoporous silica and their application in catalytic syntheses of symmetrical diselenides. Dalton Transactions (Cambridge, England : 2003). PMID 31778131 DOI: 10.1039/C9Dt03418H |
0.755 |
|
| 2019 |
De A, Santra S, Hajra A, Zyryanov GV, Majee A. Visible-Light-Induced Regioselective C(sp3)-H Acyloxylation of Aryl-2H Azirines with (Diacetoxy)iodobenzene. The Journal of Organic Chemistry. PMID 31416306 DOI: 10.1021/Acs.Joc.9B01625 |
0.611 |
|
| 2019 |
Mahato S, Mukherjee A, Santra S, Zyryanov GV, Majee A. Facile synthesis of substituted quinolines by iron(iii)-catalyzed cascade reaction between anilines, aldehydes and nitroalkanes. Organic & Biomolecular Chemistry. PMID 31414692 DOI: 10.1039/C9Ob01294J |
0.799 |
|
| 2019 |
Mahato S, Santra S, Zyryanov GV, Majee A. Metal-Free Amidation Reactions of Terminal Alkynes with Benzenesulfonamide. The Journal of Organic Chemistry. PMID 30807157 DOI: 10.1021/Acs.Joc.8B03065 |
0.792 |
|
| 2019 |
Chatterjee R, Santra S, Zyryanov G, Majee A. Vinylation of Carbonyl Oxygen in 4-Hydroxycoumarin: Synthesis of Heteroarylated Vinyl Ethers Synthesis. 51: 2371-2378. DOI: 10.1055/S-0037-1610696 |
0.785 |
|
| 2019 |
Taniya OS, Kopchuk DS, Khasanov AF, Kovalev IS, Santra S, Rahman M, Zyryanov GV, Majee A, Charushin VN, Chupakhin ON. 2-Azaanthracenes: a chronology of synthetic approaches and bright prospects for practical applications New Journal of Chemistry. 43: 11382-11390. DOI: 10.1039/C9Nj01813A |
0.331 |
|
| 2019 |
Chatterjee R, Samanta S, Mukherjee A, Santra S, Zyryanov GV, Majee A. Use of allylzinc halide as a source of halide: Differential addition of nucleophiles to Ts-aziridines and aldehydes under similar reaction conditions Tetrahedron Letters. 60: 276-283. DOI: 10.1016/J.Tetlet.2018.12.027 |
0.779 |
|
| 2019 |
Chatterjee R, Mukherjee A, Santra S, Zyryanov GV, Majee A. Iron(III)-catalyzed synthesis of selenoesters from α-amino carbonyl derivatives at room temperature Tetrahedron. 75: 130624. DOI: 10.1016/J.Tet.2019.130624 |
0.789 |
|
| 2019 |
Krinochkin AP, Kopchuk DS, Kim GA, Ganebnykh IN, Kovalev IS, Santra S, Majee A, Zyryanov GV, Rusinov VL, Chupakhin ON. Synthesis and photophysical studies of new organic-soluble lanthanide complexes of 4-(4-alkoxyphenyl)-2,2′-bipyridine-6-carboxylic acids Journal of Molecular Structure. 1176: 583-590. DOI: 10.1016/J.Molstruc.2018.08.108 |
0.346 |
|
| 2019 |
Kopchuk DS, Chepchugov NV, Starnovskaya ES, Khasanov AF, Krinochkin AP, Santra S, Zyryanov GV, Das P, Majee A, Rusinov VL, Charushin VN. Synthesis and optical properties of new 2-(5-arylpyridine-2-yl)-6-(het)arylquinoline-based “push-pull” fluorophores Dyes and Pigments. 167: 151-156. DOI: 10.1016/J.Dyepig.2019.04.029 |
0.37 |
|
| 2019 |
Starnovskaya ES, Kopchuk DS, Khasanov AF, Tanya OS, Santra S, Giri K, Rahman M, Kovalev IS, Zyryanov GV, Majee A, Charushin VN. Synthesis and photophysics of new unsymmetrically substituted 5,5′-diaryl-2,2′-bypiridine-based “push-pull” fluorophores Dyes and Pigments. 162: 324-330. DOI: 10.1016/J.Dyepig.2018.10.040 |
0.421 |
|
| 2019 |
Rahman M, Mukherjee A, Kovalev IS, Kopchuk DS, Zyryanov GV, Tsurkan MV, Majee A, Ranu BC, Charushin VN, Chupakhin ON, Santra S. Cover Picture: Recent Advances on Diverse Decarboxylative Reactions of Amino Acids (Adv. Synth. Catal. 10/2019) Advanced Synthesis & Catalysis. 361: 2160-2160. DOI: 10.1002/Adsc.201900451 |
0.544 |
|
| 2019 |
Rahman M, Mukherjee A, Kovalev IS, Kopchuk DS, Zyryanov GV, Tsurkan MV, Majee A, Ranu BC, Charushin VN, Chupakhin ON, Santra S. Recent Advances on Diverse Decarboxylative Reactions of Amino Acids Advanced Synthesis & Catalysis. 361: 2161-2214. DOI: 10.1002/Adsc.201801331 |
0.543 |
|
| 2018 |
Samanta S, Chatterjee R, Santra S, Hajra A, Khalymbadzha IA, Zyryanov GV, Majee A. Mild, Efficient, and Metal-Free Radical 1,2-Dithiocyanation of Alkynes and Alkenes at Room Temperature. Acs Omega. 3: 13081-13088. PMID 31458029 DOI: 10.1021/acsomega.8b01762 |
0.795 |
|
| 2018 |
Kopchuk DS, Nikonov IL, Khasanov AF, Giri K, Santra S, Kovalev IS, Nosova EV, Gundala S, Venkatapuram P, Zyryanov GV, Majee A, Chupakhin ON. Studies on the interactions of 5-R-3-(2-pyridyl)-1,2,4-triazines with arynes: inverse demand aza-Diels-Alder reaction versus aryne-mediated domino process. Organic & Biomolecular Chemistry. PMID 29718037 DOI: 10.1039/C8Ob00847G |
0.384 |
|
| 2018 |
Samanta S, Chatterjee R, Mahato S, Hajra A, Santra S, Zyryanov GV, Majee A. Synthesis of diverse β-(nitrooxy)-substituted amines by regioselective ring-opening of aziridines under neat conditions Synthetic Communications. 48: 1857-1866. DOI: 10.1080/00397911.2018.1471509 |
0.806 |
|
| 2017 |
Kovalev IS, Rahman M, Sadieva LK, Pavlyuk DE, Giri K, Santra S, Kopchuk DS, Zyryanov GV, Majee A, Chupakhin ON, Charushin VN. Solvent-free synthesis of (poly)thiacalix[n]arenes: the evaluation of possible mechanism based on semi-preparative HPLC separation and mass-spectrometric investigation of the reaction products Arkivoc. 2017: 159-171. DOI: 10.24820/Ark.5550190.P010.186 |
0.436 |
|
| 2017 |
Mukherjee A, Chatterjee R, De A, Satyajit S, Mahato S, Ghosal NC, Zyryanov GV, Majee A. Conjugated Addition of Amines to Electron Deficient Alkenes: A Green Approach Chimica Techno Acta. 4: 140-147. DOI: 10.15826/chimtech/2017.4.2.029 |
0.768 |
|
| 2017 |
Krinochkin AP, Kopchuk DS, Khasanov AF, Chepchugov NV, Kovalev IS, Santra S, Zyryanov GV, Majee A, Rusinov VL, Chupakhin ON. Unsymmetrically functionalized 5,5″-diaryl- and 5,6,5″-triaryl-2,2′:6′,2″-terpyridines: an efficient synthetic route and photophysical properties Canadian Journal of Chemistry. 95: 851-857. DOI: 10.1139/Cjc-2017-0195 |
0.383 |
|
| 2017 |
Mahato S, Chatterjee R, Chakraborty Ghosal N, Majee A. Zwitterionic imidazolium salt: An efficient organocatalyst for tetrahydropyranylation of alcohols Synthetic Communications. 47: 1905-1915. DOI: 10.1080/00397911.2017.1356334 |
0.813 |
|
| 2017 |
Kopchuk DS, Krinochkin AP, Khasanov AF, Kovalev IS, Slepukhin PA, Starnovskaya ES, Mukherjee A, Rahman M, Zyryanov GV, Majee A, Rusinov VL, Chupakhin ON, Santra S. An Efficient Cyanide-Free Approach towards 1-(2-Pyridyl)isoquinoline-3-carbonitriles via the Reaction of 5-Phenacyl-1,2,4-triazines with 1,2-Dehydrobenzene in the Presence of Alkyl Nitrites Synlett. 29: 483-488. DOI: 10.1055/S-0036-1590961 |
0.48 |
|
| 2017 |
Kopchuk DS, Chepchugov NV, Taniya OS, Khasanov AF, Giri K, Kovalev IS, Santra S, Zyryanov GV, Majee A, Rusinov VL, Chupakhin ON. Azaanthracenes via Inverse Electron-Demand Diels–Alder Reaction Synfacts. 13: 154-154. DOI: 10.1055/S-0036-1589931 |
0.357 |
|
| 2017 |
Mahato S, Santra S, Chatterjee R, Zyryanov GV, Hajra A, Majee A. Brønsted acidic ionic liquid-catalyzed tandem reaction: an efficient approach towards regioselective synthesis of pyrano[3,2-c]coumarins under solvent-free conditions bearing lower E-factors Green Chemistry. 19: 3282-3295. DOI: 10.1039/C7Gc01158J |
0.822 |
|
| 2017 |
Kopchuk DS, Chepchugov NV, Kovalev IS, Santra S, Rahman M, Giri K, Zyryanov GV, Majee A, Charushin VN, Chupakhin ON. Solvent-free synthesis of 5-(aryl/alkyl)amino-1,2,4-triazines and α-arylamino-2,2′-bipyridines with greener prospects Rsc Advances. 7: 9610-9619. DOI: 10.1039/C6Ra26305D |
0.543 |
|
| 2017 |
Ojha NK, Zyryanov GV, Majee A, Charushin VN, Chupakhin ON, Santra S. Copper nanoparticles as inexpensive and efficient catalyst: A valuable contribution in organic synthesis Coordination Chemistry Reviews. 353: 1-57. DOI: 10.1016/J.Ccr.2017.10.004 |
0.425 |
|
| 2017 |
Krinochkin AP, Kopchuk DS, Chepchugov NV, Kim GA, Kovalev IS, Rahman M, Zyryanov GV, Majee A, Rusinov VL, Chupakhin ON. An efficient synthetic approach towards new 5,5’-diaryl-2,2’-bipyridine-based fluorophores Chinese Chemical Letters. 28: 1099-1103. DOI: 10.1016/J.Cclet.2016.12.043 |
0.364 |
|
| 2017 |
Das S, Santra S, Jana S, Zyryanov GV, Majee A, Hajra A. The Remarkable Cooperative Effect of a Brønsted‐Acidic Ionic Liquid in the Cyclization of 2‐Aminobenzamides with Ketones European Journal of Organic Chemistry. 2017: 4955-4962. DOI: 10.1002/Ejoc.201700966 |
0.549 |
|
| 2016 |
Santra S, Kundu SK, Ghosal NC, Chatterjee R, Mahato S, Khalymbadzha IA, Zyryanov GV, Hajra A, Majee A. Combination of NH2OH·HCl and NaIO4: a new and mild reagent for the synthesis of vicinal diiodo carbonyl compounds Arkivoc. 2016: 416-426. DOI: 10.24820/Ark.5550190.P009.698 |
0.792 |
|
| 2016 |
Bagdi A, Kundu D, Majee A, Hajra A. Zwitterionic Imidazolium Salt: An Efficient Organocatalyst for the One-Pot Synthesis of 5,6-Unsubstituted 1,4-Dihydropyridine Scaffolds Current Organocatalysis. 3: 169-175. DOI: 10.2174/2213337202666150414201734 |
0.604 |
|
| 2016 |
Das S, Santra S, Mondal P, Majee A, Hajra A. Zwitterionic Imidazolium Salt: Recent Advances in Organocatalysis Synthesis (Germany). 48: 1269-1285. DOI: 10.1055/S-0035-1561336 |
0.685 |
|
| 2016 |
Sarkar A, Santra S, Kundu SK, Hajra A, Zyryanov GV, Chupakhin ON, Charushin VN, Majee A. A decade update on solvent and catalyst-free neat organic reactions: a step forward towards sustainability Green Chemistry. 18: 4475-4525. DOI: 10.1039/C6Gc01279E |
0.621 |
|
| 2016 |
Santra S, Kopchuk DS, Kovalev IS, Zyryanov GV, Majee A, Charushin VN, Chupakhin ON. Solvent-free synthesis of pillar[6]arenes Green Chemistry. 18: 423-426. DOI: 10.1039/C5Gc01505G |
0.479 |
|
| 2016 |
Chakraborty Ghosal N, Santra S, Das S, Hajra A, Zyryanov GV, Majee A. Organocatalysis by an aprotic imidazolium zwitterion: Regioselective ring-opening of aziridines and applicable to gram scale synthesis Green Chemistry. 18: 565-574. DOI: 10.1039/C5Gc01323B |
0.652 |
|
| 2016 |
Kopchuk DS, Chepchugov NV, Taniya OS, Khasanov AF, Giri K, Kovalev IS, Santra S, Zyryanov GV, Majee A, Rusinov VL, Chupakhin ON. 3-Cyano-2-azaanthracene-based “push-pull” fluorophores: A one-step preparation from 5-cyano-1,2,4-triazines and 2,3-dehydronaphthalene, generated in situ Tetrahedron Letters. 57: 5639-5643. DOI: 10.1016/J.Tetlet.2016.11.008 |
0.422 |
|
| 2016 |
Kopchuk DS, Chepchugov NV, Khasanov AF, Kovalev IS, Santra S, Nosova EV, Zyryanov GV, Majee A, Rusinov VL, Chupakhin ON. A one-pot approach to 10-(1H-1,2,3-triazol-1-yl)pyrimido[1,2-a]indoles via aryne-mediated transformations of 3-(pyrimidin-2-yl)-1,2,4-triazines Tetrahedron Letters. 57: 3862-3865. DOI: 10.1016/J.Tetlet.2016.07.052 |
0.476 |
|
| 2016 |
Ghosal NC, Santra S, Zyryanov GV, Hajra A, Majee A. Conversion of aziridines to oxazolidines through geminal difunctionalization of vinyl arenes or by tandem ring-opening/closing reaction of aziridine itself Tetrahedron Letters. 57: 3551-3555. DOI: 10.1016/J.Tetlet.2016.06.119 |
0.654 |
|
| 2016 |
Ghosal NC, Santra S, Zyryanov GV, Hajra A, Majee A. ChemInform Abstract: Conversion of Aziridines to Oxazolidines Through Geminal Difunctionalization of Vinyl Arenes or by Tandem Ring-Opening/Closing Reaction of Aziridine Itself. Cheminform. 47. DOI: 10.1002/CHIN.201647144 |
0.602 |
|
| 2016 |
Das S, Santra S, Mondal P, Majee A, Hajra A. ChemInform Abstract: Zwitterionic Imidazolium Salt: Recent Advances in Organocatalysis Cheminform. 47. DOI: 10.1002/CHIN.201627257 |
0.459 |
|
| 2016 |
Chakraborty Ghosal N, Santra S, Das S, Hajra A, Zyryanov GV, Majee A. ChemInform Abstract: Organocatalysis by an Aprotic Imidazolium Zwitterion: Regioselective Ring-Opening of Aziridines and Applicable to Gram Scale Synthesis. Cheminform. 47. DOI: 10.1002/CHIN.201623042 |
0.546 |
|
| 2015 |
Monir K, Ghosh M, Jana S, Mondal P, Majee A, Hajra A. Regioselective synthesis of nitrosoimidazoheterocycles using tert-butyl nitrite. Organic & Biomolecular Chemistry. 13: 8717-22. PMID 26178232 DOI: 10.1039/C5Ob01345C |
0.805 |
|
| 2015 |
Sarkar A, Santra S, Kundu SK, Ghosal NC, Hajra A, Majee A. Zinc Tetrafluoroborate: A versatile and robust catalyst for various organic reactions and transformations Synthesis (Germany). 47: 1379-1386. DOI: 10.1055/S-0034-1380168 |
0.712 |
|
| 2015 |
Santra S, Kovalev IS, Kopchuk DS, Zyryanov GV, Majee A, Charushin VN, Chupakhin ON. Role of polar solvents for the synthesis of pillar[6]arenes Rsc Advances. 5: 104284-104288. DOI: 10.1039/C5Ra19569A |
0.419 |
|
| 2015 |
Chakraborty N, Santra S, Kundu SK, Hajra A, Zyryanov GV, Majee A. Combination of NH2OH·HCl and NaIO4: an effective reagent for molecular iodine-free regioselective 1,2-difunctionalization of olefins and easy access of terminal acetals Rsc Advances. 5: 56780-56788. DOI: 10.1039/C5Ra11092K |
0.782 |
|
| 2015 |
Kundu SK, Mitra K, Majee A. Copper(i) iodide catalyzed synthesis of primary propargylic alcohols from terminal alkyne Rsc Advances. 5: 13220-13223. DOI: 10.1039/C4Ra12719F |
0.396 |
|
| 2015 |
Das S, Bagdi AK, Santra S, Majee A, Hajra A. Solvent-free silica-promoted multicomponent condensation: synthesis of highly functionalized piperidines Research On Chemical Intermediates. 41: 6749-6763. DOI: 10.1007/S11164-014-1774-7 |
0.675 |
|
| 2015 |
Chakraborty N, Santra S, Kundu SK, Hajra A, Zyryanov GV, Majee A. ChemInform Abstract: Combination of NH2OH·HCl and NaIO4: An Effective Reagent for Molecular Iodine-Free Regioselective 1,2-Difunctionalization of Olefins and Easy Access of Terminal Acetals. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201546081 |
0.538 |
|
| 2015 |
Sarkar A, Santra S, Kundu SK, Ghosal NC, Hajra A, Majee A. ChemInform Abstract: Zinc Tetrafluoroborate: A Versatile and Robust Catalyst for Various Organic Reactions and Transformations Cheminform. 46: no-no. DOI: 10.1002/CHIN.201529288 |
0.57 |
|
| 2014 |
Mitra S, Chakraborty A, Mishra S, Majee A, Hajra A. Copper(I)-catalyzed oxidative coupling between 2-aminobenzothiazole and terminal alkyne: formation of benzothiazine. Organic Letters. 16: 5652-5. PMID 25325187 DOI: 10.1021/Ol502729C |
0.732 |
|
| 2014 |
Santra S, Rahman M, Roy A, Majee A, Hajra A. Microwave-Assisted Three-Component “Catalyst and Solvent-Free” Green Protocol: A Highly Efficient and Clean One-Pot Synthesis of Tetrahydrobenzo[b]pyrans Organic Chemistry International. 2014: 1-8. DOI: 10.1155/2014/851924 |
0.664 |
|
| 2014 |
Rahman M, Roy A, Ghosh M, Mitra S, Majee A, Hajra A. Organocatalysis by an aprotic imidazolium zwitterion: a dramatic anion–cation cooperative effect on azide–nitrile cycloaddition Rsc Advances. 4: 6116. DOI: 10.1039/C3Ra46293E |
0.643 |
|
| 2014 |
Santra S, Mitra S, Bagdi AK, Majee A, Hajra A. Iron(III)-catalyzed three-component domino strategy for the synthesis of imidazo[1,2-a]pyridines Tetrahedron Letters. 55: 5151-5155. DOI: 10.1016/J.Tetlet.2014.07.094 |
0.695 |
|
| 2014 |
Rahman M, Sarkar A, Ghosh M, Majee A, Hajra A. Catalytic application of task specific ionic liquid on the synthesis of benzoquinazolinone derivatives by a multicomponent reaction Tetrahedron Letters. 55: 235-239. DOI: 10.1016/J.Tetlet.2013.11.011 |
0.675 |
|
| 2014 |
Santra S, Rahman M, Roy A, Majee A, Hajra A. Nano-indium oxide: An efficient catalyst for one-pot synthesis of 2,3-dihydroquinazolin-4(1H)-ones with a greener prospect Catalysis Communications. 49: 52-57. DOI: 10.1016/J.Catcom.2014.01.032 |
0.643 |
|
| 2014 |
Majee A, Kundu SK, Santra S, Hajra A. ChemInform Abstract: An Improved Procedure of Miyashita Protocol for the Preparation of Ureidomethylene Derivatives of 1,3-Dicarbonyl Compounds. Cheminform. 45: no-no. DOI: 10.1002/CHIN.201420049 |
0.503 |
|
| 2014 |
Monir K, Kumar Bagdi A, Mishra S, Majee A, Hajra A. Copper(II)-Catalyzed Aerobic Oxidative Coupling between Chalcone and 2-AminopyridineviaCH Amination: An Expedient Synthesis of 3-Aroylimidazo[1,2-a]pyridines Advanced Synthesis & Catalysis. 356: 1105-1112. DOI: 10.1002/Adsc.201300900 |
0.798 |
|
| 2013 |
Bagdi AK, Santra S, Rahman M, Majee A, Hajra A. Synthesis of polysubstituted quinolines via copper(ii)-catalyzed annulation of 2-aminoaryl ketones with alkynoates Rsc Advances. 3: 24034. DOI: 10.1039/C3Ra45576A |
0.673 |
|
| 2013 |
Santra S, Bagdi AK, Majee A, Hajra A. Metal nanoparticles in “on-water” organic synthesis: one-pot nano CuO catalyzed synthesis of isoindolo[2,1-a]quinazolines Rsc Advances. 3: 24931. DOI: 10.1039/C3Ra43917H |
0.691 |
|
| 2013 |
Kundu SK, Mitra K, Majee A. Dialkyl phosphite as a highly selective mono-N-alkylating agent using indium triflate under microwave irradiation Rsc Advances. 3: 8649. DOI: 10.1039/C3Ra40509E |
0.35 |
|
| 2013 |
Mitra S, Bagdi AK, Majee A, Hajra A. Nano indium oxide catalyzed tandem cyclization of amidine with nitroolefin Tetrahedron Letters. 54: 4982-4985. DOI: 10.1016/J.Tetlet.2013.07.050 |
0.672 |
|
| 2013 |
Bagdi AK, Majee A, Hajra A. Regioselective synthesis of pyrano[3,2-c]coumarins via Cu(II)-catalyzed tandem reaction Tetrahedron Letters. 54: 3892-3895. DOI: 10.1016/J.Tetlet.2013.05.061 |
0.688 |
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| 2013 |
Monir K, Ghosh M, Mishra S, Majee A, Hajra A. Phenyliodine(III) Diacetate (PIDA) Mediated Synthesis of Aromatic Azo Compounds through Oxidative Dehydrogenative Coupling of Anilines: Scope and Mechanism European Journal of Organic Chemistry. 2014: 1096-1102. DOI: 10.1002/Ejoc.201301209 |
0.829 |
|
| 2013 |
Roy A, Majee A, Hajra A. ChemInform Abstract: A Mild and Efficient Synthesis of 1,5-Benzodiazepine Derivatives Catalyzed by Acidic Ionic Liquid in Solvent-Free Condition. Cheminform. 44: no-no. DOI: 10.1002/CHIN.201313173 |
0.6 |
|
| 2013 |
Bagdi AK, Rahman M, Santra S, Majee A, Hajra A. Copper-Catalyzed Synthesis of Imidazo[1,2-a]pyridines through Tandem Imine Formation-Oxidative Cyclization under Ambient Air: One-Step Synthesis of Zolimidine on a Gram-Scale Advanced Synthesis & Catalysis. 355: 1741-1747. DOI: 10.1002/Adsc.201300298 |
0.652 |
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| 2013 |
Santra S, Bagdi AK, Majee A, Hajra A. Iron(III)-Catalyzed Cascade Reaction between Nitroolefins and 2-Aminopyridines: Synthesis of Imidazo[1,2-a]pyridines and Easy Access towards Zolimidine Advanced Synthesis & Catalysis. 355: 1065-1070. DOI: 10.1002/Adsc.201201112 |
0.665 |
|
| 2012 |
Das S, Santra S, Roy A, Urinda S, Majee A, Hajra A. One-pot multicomponent synthesis of polyhydroquinolines under catalyst and solvent-free conditions Green Chemistry Letters and Reviews. 5: 97-100. DOI: 10.1080/17518253.2011.584073 |
0.692 |
|
| 2012 |
Rahman M, Ghosh M, Hajra A, Majee A. A simple and efficient approach for the sulfonylation of indoles catalyzed by CuI Journal of Sulfur Chemistry. 34: 342-346. DOI: 10.1080/17415993.2012.740672 |
0.682 |
|
| 2012 |
Kundu SK, Rahman M, Dhara P, Hajra A, Majee A. Efficient and Alternative Approach for Preparation of O-Benzoyloximes Using Benzoyl Peroxide Synthetic Communications. 42: 1848-1854. DOI: 10.1080/00397911.2010.545165 |
0.62 |
|
| 2012 |
Majee A, Kundu SK, Santra S, Hajra A. Combination of NH2OH·HCl and NaIO4: a new and mild oxidizing agent for selective oxidation of alcohols to carbonyl compounds Tetrahedron Letters. 53: 4433-4435. DOI: 10.1016/J.Tetlet.2012.06.043 |
0.595 |
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| 2012 |
Santra S, Majee A, Hajra A. Nano indium oxide: an efficient catalyst for the synthesis of 1,2-disubstituted benzimidazoles in aqueous media Tetrahedron Letters. 53: 1974-1977. DOI: 10.1016/J.Tetlet.2012.02.021 |
0.662 |
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| 2012 |
Rahman M, Bagdi AK, Kundu D, Majee A, Hajra A. Zwitterionic-Type Molten Salt-Catalyzed Multicomponent Reactions: One-Pot Synthesis of Substituted Imidazoles Under Solvent-Free Conditions Journal of Heterocyclic Chemistry. 49: 1224-1228. DOI: 10.1002/Jhet.924 |
0.702 |
|
| 2012 |
Majee A, Kundu SK, Santra S, Hajra A. ChemInform Abstract: Combination of NH2OH·HCl and NaIO4: A New and Mild Oxidizing Agent for Selective Oxidation of Alcohols to Carbonyl Compounds. Cheminform. 43: no-no. DOI: 10.1002/CHIN.201246071 |
0.478 |
|
| 2012 |
Kundu SK, Rahman M, Dhara P, Hajra A, Majee A. ChemInform Abstract: Efficient and Alternative Approach for Preparation of O-Benzoyloximes Using Benzoyl Peroxide. Cheminform. 43: no-no. DOI: 10.1002/CHIN.201237061 |
0.481 |
|
| 2012 |
Santra S, Majee A, Hajra A. ChemInform Abstract: Nano Indium Oxide: An Efficient Catalyst for the Synthesis of 1,2-Disubstituted Benzimidazoles in Aqueous Media. Cheminform. 43: no-no. DOI: 10.1002/CHIN.201230138 |
0.586 |
|
| 2011 |
Kundu D, Samim M, Majee A, Hajra A. Indium triflate-catalyzed coupling between nitroalkenes and phenol/naphthols: a simple and direct synthesis of arenofurans by a cyclization reaction. Chemistry, An Asian Journal. 6: 406-9. PMID 21254418 DOI: 10.1002/Asia.201000869 |
0.685 |
|
| 2011 |
Das S, Majee A, Hajra A. A convenient synthesis of coumarins using reusable ionic liquid as catalyst Green Chemistry Letters and Reviews. 4: 349-353. DOI: 10.1080/17518253.2011.572296 |
0.634 |
|
| 2011 |
Kundu D, Majee A, Hajra A. Task-specific ionic liquid catalyzed efficient microwave-assisted synthesis of 12-alkyl or aryl-8,9,10,12-tetrahydrobenzo[a]xanthen-11-ones under solvent-free conditions Green Chemistry Letters and Reviews. 4: 205-209. DOI: 10.1080/17518253.2010.544260 |
0.682 |
|
| 2011 |
Rahman M, Bagdi AK, Majee A, Hajra A. Synthesis of Propargylamines with In2O3 Nanoparticles Synfacts. 2011: 1140-1140. DOI: 10.1055/S-0030-1261085 |
0.53 |
|
| 2011 |
Kundu D, Bagdi AK, Majee A, Hajra A. Zwitterionic-Type Molten Salt: A Mild and Efficient Organocatalyst for the Synthesis of 3-Aminoalkylated Indoles via Three-Component Coupling Reaction Synlett. 2011: 1165-1167. DOI: 10.1055/S-0030-1259940 |
0.699 |
|
| 2011 |
Rahman M, Bagdi AK, Majee A, Hajra A. Nano indium oxide catalyzed efficient synthesis of propargylamines via C–H and C–Cl bond activations Tetrahedron Letters. 52: 4437-4439. DOI: 10.1016/J.Tetlet.2011.06.067 |
0.69 |
|
| 2011 |
Santra S, Majee A, Hajra A. Task-specific ionic liquid-catalyzed efficient couplings of indoles with 1,3-dicarbonyl compounds: an efficient synthesis of 3-alkenylated indoles Tetrahedron Letters. 52: 3825-3827. DOI: 10.1016/J.Tetlet.2011.05.069 |
0.648 |
|
| 2011 |
Santra S, Majee A, Hajra A. ChemInform Abstract: Task-Specific Ionic Liquid-Catalyzed Efficient Couplings of Indoles with 1,3-Dicarbonyl Compounds: An Efficient Synthesis of 3-Alkenylated Indoles Cheminform. 42: no-no. DOI: 10.1002/CHIN.201144106 |
0.578 |
|
| 2010 |
Roy A, Kundu D, Kundu SK, Majee A, Hajra A. Manganese (II) Chloride-Catalyzed Conjugated Addition of Amines to Electron Deficient Alkenes in Methanol-Water Medium~!2009-10-16~!2009-12-15~!2010-03-30~! The Open Catalysis Journal. 3: 34-39. DOI: 10.2174/1876214X01003010034 |
0.57 |
|
| 2010 |
Das S, Rahman M, Kundu D, Majee A, Hajra A. Task-specific ionic-liquid-catalyzed efficient synthesis of indole derivatives under solvent-free conditions Canadian Journal of Chemistry. 88: 150-154. DOI: 10.1139/V09-154 |
0.612 |
|
| 2010 |
Kundu SK, Islam S, Hajra A, Majee A. Tetrabutylammonium tribromide as efficient catalyst in the synthesis of bis(indolyl)methanes Russian Journal of Organic Chemistry. 46: 126-128. DOI: 10.1134/S1070428010010136 |
0.653 |
|
| 2010 |
Rahman M, Kundu D, Hajra A, Majee A. Corrigendum to “Formylation without catalyst and solvent at 80 °C” [Tetrahedron Lett. 51 (2010) 2896] Tetrahedron Letters. 51: 4584-4585. DOI: 10.1016/J.Tetlet.2010.06.111 |
0.566 |
|
| 2010 |
Rahman M, Kundu D, Hajra A, Majee A. Formylation without catalyst and solvent at 80 °C Tetrahedron Letters. 51: 2896-2899. DOI: 10.1016/J.Tetlet.2010.03.097 |
0.622 |
|
| 2010 |
Kundu D, Majee A, Hajra A. Zwitterionic-type molten salt: An efficient mild organocatalyst for synthesis of 2-amidoalkyl and 2-carbamatoalkyl naphthols Catalysis Communications. 11: 1157-1159. DOI: 10.1016/J.Catcom.2010.06.001 |
0.665 |
|
| 2010 |
Rahman M, Majee A, Hajra A. Microwave-assisted Brønsted acidic ionic liquid-promoted one-pot synthesis of heterobicyclic dihydropyrimidinones by a three-component coupling of cyclopentanone, aldehydes, and urea Journal of Heterocyclic Chemistry. 47: 1230-1233. DOI: 10.1002/Jhet.415 |
0.608 |
|
| 2010 |
Atlan V, Elkaim L, Grimaud L, Jana NK, Majee A. ChemInform Abstract: The Mannich Reaction of Hydrazones Amenable to Solid Phase Synthesis: A Powerful Tool for Heterocycle Preparation. Cheminform. 33: no-no. DOI: 10.1002/CHIN.200225112 |
0.313 |
|
| 2010 |
Ranu BC, Jana U, Majee A. ChemInform Abstract: A Simple and Efficient Method for Selective Deprotection of t-Butyldimethylsilyl Ethers by Zinc Tetrafluoroborate in Water. Cheminform. 30: no-no. DOI: 10.1002/CHIN.199923087 |
0.44 |
|
| 2010 |
Majee A, Das AR, Ranu BC. ChemInform Abstract: Zinc Mediated Allylation of Aldehydes and Ketones Using Allyl Bromides and Commercial Zinc Dust. The Issue of Regio- and Stereoselectivity. Cheminform. 30: no-no. DOI: 10.1002/CHIN.199909043 |
0.547 |
|
| 2010 |
RANU BC, MAJEE A, SARKAR A. ChemInform Abstract: One-Pot Reductive Amination of Conjugated Aldehydes and Ketones with Silica Gel and Zinc Borohydride. Cheminform. 29: no-no. DOI: 10.1002/CHIN.199823056 |
0.563 |
|
| 2010 |
RANU BC, MAJEE A, DAS AR. ChemInform Abstract: A Convenient Synthesis of β,γ-Unsaturated Ketones Through Zinc-Mediated Allylation of Acid Chlorides. Cheminform. 27: no-no. DOI: 10.1002/chin.199622078 |
0.525 |
|
| 2010 |
RANU BC, MAJEE A, DAS AR. ChemInform Abstract: Surface-Mediated Solid Phase Reaction. Part 7. A Simple and Convenient Procedure for the Methoxymethylation of Alcohols with Methoxymethyl Chloride on the Surface of Alumina. Cheminform. 26: no-no. DOI: 10.1002/chin.199525077 |
0.458 |
|
| 2009 |
Rahman M, Roy A, Majee A, Hajra A. Synthesis of 1,5-benzothiazepines with microwave irradiation under solvent and catalyst-free conditions Journal of Chemical Research-S. 2009: 178-179. DOI: 10.3184/030823409X416965 |
0.651 |
|
| 2009 |
Roy A, Rahman M, Das S, Kundu D, Kundu SK, Majee A, Hajra A. Zinc Chloride as an Efficient Catalyst for Chemoselective Dimethyl Acetalization Synthetic Communications. 39: 590-595. DOI: 10.1080/00397910802412859 |
0.638 |
|
| 2009 |
Kundu D, Debnath RK, Majee A, Hajra A. Zwitterionic-type molten salt-catalyzed syn-selective aza-Henry reaction: solvent-free one-pot synthesis of β-nitroamines Tetrahedron Letters. 50: 6998-7000. DOI: 10.1016/J.Tetlet.2009.09.153 |
0.679 |
|
| 2009 |
Kundu D, Majee A, Hajra A. Indium triflate-catalyzed one-pot synthesis of 1-substituted-1H-1,2,3,4-tetrazoles under solvent-free conditions Tetrahedron Letters. 50: 2668-2670. DOI: 10.1016/J.Tetlet.2009.03.131 |
0.685 |
|
| 2009 |
Hajra A, Kundu D, Majee A. An efficient one-pot synthesis of naphthoxazinones by a three-component coupling of naphthol, aldehydes, and urea catalyzed by zinc triflate Journal of Heterocyclic Chemistry. 46: 1019-1022. DOI: 10.1002/Jhet.180 |
0.65 |
|
| 2009 |
Urinda S, Kundu D, Majee A, Hajra A. Indium triflate-catalyzed one-pot synthesis of 14-alkyl or aryl-14H-dibenzo[a, j]xanthenes in water Heteroatom Chemistry. 20: 232-234. DOI: 10.1002/Hc.20539 |
0.673 |
|
| 2009 |
Kundu SK, Majee A, Hajra A. ChemInform Abstract: Environmentally Benign Aqueous Zinc Tetrafluoroborate-Catalyzed One-Pot Biginelli Condensation at Room Temperature. Cheminform. 40. DOI: 10.1002/CHIN.200928142 |
0.514 |
|
| 2008 |
Kundu D, Kundu SK, Majee A, Hajra A. A Facile Synthesis of 2,2,4-Trisubstituted-1,2-Dihydroquinolines Catalyzed by Zinc Triflate under Solvent-Free Conditions Journal of the Chinese Chemical Society. 55: 1186-1190. DOI: 10.1002/Jccs.200800175 |
0.684 |
|
| 2008 |
Kundu D, Majee A, Hajra A. L‐Proline Catalyzed Enamination of β‐Dicarbonyl Compounds under Solvent‐free Conditions Chinese Journal of Chemistry. 26: 1545-1548. DOI: 10.1002/Cjoc.200890279 |
0.634 |
|
| 2007 |
Chattopadhyay T, Islam S, Nethaji M, Majee A, Das D. Mono- and bi-metallic Mn(III) complexes of macroacyclic salen type ligands: Syntheses, characterization and studies of their catalytic activity Journal of Molecular Catalysis a: Chemical. 267: 255-264. DOI: 10.1016/J.Molcata.2006.11.053 |
0.308 |
|
| 2006 |
Majee A, Kundu SK, Islam S. Mild and Efficient Method for Oxathioacetalization of Carbonyl Compounds Synthetic Communications. 36: 3767-3770. DOI: 10.1080/00397910600947783 |
0.421 |
|
| 2005 |
Islam S, Majee A, Khan AT. Tetrahydropyranylation and Depyranylation of Alcohols Catalyzed by Aqueous Zinc Tetrafluoroborate Synthetic Communications. 35: 1789-1793. DOI: 10.1081/Scc-200063950 |
0.325 |
|
| 2005 |
Khan AT, Islam S, Majee A, Chattopadhyay T, Ghosh S. Bromodimethylsulfonium bromide: A useful reagent for acylation of alcohols, phenols, amines, thiols, thiophenols and 1,1-diacylation of aldehydes under solvent free conditions Journal of Molecular Catalysis a: Chemical. 239: 158-165. DOI: 10.1016/J.Molcata.2005.05.042 |
0.502 |
|
| 2005 |
Khan AT, Sahu P, Majee A. A highly efficient and catalytic synthetic protocol for oxathioacetalization of carbonyl compounds Journal of Molecular Catalysis a: Chemical. 226: 207-212. DOI: 10.1016/J.Molcata.2004.10.019 |
0.54 |
|
| 2004 |
Islam S, Majee A, Mandal T, Khan AT. Selective Thioacetalization of Aldehydes Catalyzed by Aqueous Zinc Tetrafluoroborate Synthetic Communications. 34: 2911-2916. DOI: 10.1081/Scc-200026628 |
0.382 |
|
| 2002 |
Atlan V, Elkaim L, Grimaud L, Jana NK, Majee A. The Mannich Reaction of Hydrazones Amenable to Solid Phase Synthesis: A Powerful Tool for Heterocycle Preparation Synlett. 2002: 0352-0354. DOI: 10.1055/S-2002-19745 |
0.476 |
|
| 2000 |
Atlan V, Bienaymé H, Kaim LE, Majee A. The use of hydrazones for efficient mannich type coupling with aldehydes and secondary amines Chemical Communications. 1585-1586. DOI: 10.1039/B002750M |
0.481 |
|
| 1999 |
Ranu BC, Jana U, Majee A. Selective monoacylation of ferrocene Green Chemistry. 1: 33-34. DOI: 10.1039/A808890J |
0.544 |
|
| 1999 |
Ranu BC, Jana U, Majee A. A simple and efficient method for selective deprotection of t-butyldimethylsilyl ethers by zinc tetrafluoroborate in water Tetrahedron Letters. 40: 1985-1988. DOI: 10.1016/S0040-4039(99)00097-0 |
0.506 |
|
| 1997 |
Ranu BC, Majee A. Indium-Mediated Regioselective Markovnikov Allylation Of Unactivated Terminal Alkynes Chemical Communications. 1225-1226. DOI: 10.1039/A702241G |
0.566 |
|
| 1997 |
Ranu BC, Sarkar aA, Majee A. Reduction of Imines with Zinc Borohydride Supported on Silica Gel. Highly Stereoselective Synthesis of Substituted Cyclohexylamines Journal of Organic Chemistry. 62: 1841-1842. DOI: 10.1021/Jo961736A |
0.622 |
|
| 1996 |
Ranu BC, Majee A, Das AR. A convenient synthesis of β,γ-unsaturated ketones through zinc-mediated allylation of acid chlorides Tetrahedron Letters. 37: 1109-1112. DOI: 10.1016/0040-4039(95)02317-8 |
0.76 |
|
| 1995 |
Ranu BC, Majee A, Das AR. Surface-Mediated Solid Phase Reaction. PART 7.1A Simple and Convenient Procedure for the Methoxymethylation of Alcohols with Methoxymethyl Chloride on the Surface of Alumina Synthetic Communications. 25: 363-367. DOI: 10.1080/00397919508011367 |
0.534 |
|
| 1995 |
Ranu BC, Majee A, Das AR. Facile and efficient synthesis of homoallylic alcohols using allyl bromide and commercial zinc dust Tetrahedron Letters. 36: 4885-4888. DOI: 10.1016/0040-4039(95)00877-F |
0.746 |
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