Year |
Citation |
Score |
2023 |
Pal K, Chandu P, Das D, Jinilkumar AV, Mallick M, Sureshkumar D. Organophotocatalyzed Mono- and Bis-Alkyl/Difluoroalkylative Thio/Selenocyanation of Alkenes. The Journal of Organic Chemistry. PMID 37988569 DOI: 10.1021/acs.joc.3c02102 |
0.673 |
|
2023 |
Das D, Ghosh KG, Garai S, Palasetty C, Devarajulu S. An organo-photocatalyzed visible-light-driven multi-component approach for carbothioaryl/alkylation of activated alkenes C(sp)-H bond functionalization. Organic & Biomolecular Chemistry. 21: 7724-7729. PMID 37691553 DOI: 10.1039/d3ob01150j |
0.757 |
|
2023 |
Srinivasu V, Das D, Chandu P, Ghosh KG, Sureshkumar D. Metal-Free Photoredox Four-Component Strategy to 1,3-Functionalized BCP Derivatives. Organic Letters. PMID 37417829 DOI: 10.1021/acs.orglett.3c01877 |
0.713 |
|
2022 |
Ghosh KG, Das D, Garai S, Chandu P, Sureshkumar D. Visible-Light-Driven Organophotocatalyzed Multicomponent Approach for Tandem C(sp)-H Activation and Alkylation Followed by Trifluoromethylthiolation. The Journal of Organic Chemistry. PMID 35730650 DOI: 10.1021/acs.joc.2c00783 |
0.723 |
|
2021 |
Ghosh KG, Das D, Chandu P, Sureshkumar D. Visible-Light-Driven Organophotocatalyzed Mono-, Di-, and Tri-C(sp)-H Alkylation of Phosphoramides. The Journal of Organic Chemistry. PMID 33440934 DOI: 10.1021/acs.joc.0c02695 |
0.733 |
|
2020 |
Das D, Ghosh KG, Chandu P, Sureshkumar D. Ammonium Chloride-Mediated Trifluoromethylthiolation of -Quinone Methides. The Journal of Organic Chemistry. PMID 33107737 DOI: 10.1021/acs.joc.0c01752 |
0.757 |
|
2019 |
Das DK, Kannaujiya VK, Sadhu MM, Ray SK, Singh VK. BF3·OEt2 Catalyzed Vinyl Azides Addition to in situ Generated N-Acyl Iminium Salts: Synthesis of 3-Oxoisoindoline-1-acetamides. The Journal of Organic Chemistry. PMID 31741383 DOI: 10.1021/Acs.Joc.9B02127 |
0.441 |
|
2019 |
Chandu P, Ghosh KG, Das D, Sureshkumar D. Photoredox catalysed allylic trifluoromethylation via ring opening of vinyl cyclopropanes using Langlois reagent Tetrahedron. 75: 130641. DOI: 10.1016/J.Tet.2019.130641 |
0.723 |
|
2017 |
Zhang G, Xu W, Liu J, Das DK, Yang S, Perveen S, Zhang H, Li X, Fang X. Enantioselective intermolecular all-carbon [4+2] annulation via N-heterocyclic carbene organocatalysis. Chemical Communications (Cambridge, England). PMID 29188838 DOI: 10.1039/C7Cc08680F |
0.315 |
|
2016 |
Zhang G, Yang S, Zhang X, Lin Q, Das DK, Liu J, Fang X. Dynamic Kinetic Resolution Enabled by Intramolecular Benzoin Reaction: Synthetic Applications and Mechanistic Insights. Journal of the American Chemical Society. PMID 27270409 DOI: 10.1021/Jacs.6B02929 |
0.369 |
|
2016 |
Lin Q, Li Y, Das DK, Zhang G, Zhao Z, Yang S, Fang X. N-Heterocyclic carbene-catalyzed desymmetrization of functionalized 1,4-dienes via Stetter Reaction. Chemical Communications (Cambridge, England). PMID 27100939 DOI: 10.1039/C6Cc01011C |
0.364 |
|
2016 |
Lin Q, Li Y, Das DK, Zhang G, Zhao Z, Yang S, Fang X. ChemInform Abstract: N-Heterocyclic Carbene-Catalyzed Desymmetrization of Functionalized 1,4-Dienes via Stetter Reaction. Cheminform. 47. DOI: 10.1002/CHIN.201638108 |
0.314 |
|
2016 |
Islam K, Das DK, Akram E, Khan AT. ChemInform Abstract: Exploration of C5-C6-Unsubstituted 1,4-Dihydropyridines for the Construction of exo-Hexahydro-1H-chromeno[3,4-h][1,6]naphthyridine-3-carboxylates Using a Stereoselective Povarov Reaction. Cheminform. 47: no-no. DOI: 10.1002/CHIN.201606078 |
0.351 |
|
2015 |
Islam K, Das DK, Akram E, Khan AT. Exploration of C5–C6-Unsubstituted 1,4-Dihydropyridines for the Construction of exo-Hexahydro-1H-chromeno[3,4-h][1,6]naphthyridine-3-carboxylates Using a Stereoselective Povarov Reaction Synthesis (Germany). DOI: 10.1055/S-0034-1380431 |
0.358 |
|
2015 |
Belal M, Das DK, Khan AT. Synthesis of pyrido[2,3-c]coumarin derivatives by an intramolecular povarov reaction Synthesis (Germany). 47: 1109-1116. DOI: 10.1055/S-0034-1380131 |
0.432 |
|
2015 |
Islam K, Sidick Basha R, Dar AA, Das DK, Khan AT. A direct approach for the expedient synthesis of unsymmetrical ethers by employing bromodimethylsulfonium bromide (BDMS) mediated C-S bond cleavage of naphthalene-2-ol sulfides Rsc Advances. 5: 79759-79764. DOI: 10.1039/C5Ra14563E |
0.405 |
|
2015 |
Bhattacharjee S, Das DK, Khan AT. Bromodimethylsulfonium bromide: An efficient catalyst for one-pot synthesis of 4-phenacylidene flavene derivatives Tetrahedron Letters. 56: 2412-2415. DOI: 10.1016/J.Tetlet.2015.03.047 |
0.398 |
|
2015 |
Belal M, Das DK, Khan AT. ChemInform Abstract: Synthesis of Pyrido[2,3-c]coumarin Derivatives by an Intramolecular Povarov Reaction. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201535166 |
0.437 |
|
2015 |
Sarkar S, Das DK, Khan AT. ChemInform Abstract: Synthesis of Fully-Substituted Pyridines and Dihydropyridines in a Highly Chemoselective Manner Utilizing a Multicomponent Reaction (MCR) Strategy. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201517203 |
0.4 |
|
2015 |
Islam K, Das DK, Khan AT. ChemInform Abstract: Hydrated Ferric Sulfate Catalyzed Synthesis of 5,6-Unsubstituted 1,4-Dihydropyridines Using Three-Component Reaction. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201511209 |
0.368 |
|
2014 |
Bhattacharjee S, Das DK, Khan AT. Ammonium chloride-catalyzed three-component reaction for the synthesis of fused 4H-chromene derivatives in aqueous medium Synthesis (Germany). 46: 73-80. DOI: 10.1055/S-0033-1340082 |
0.41 |
|
2014 |
Sarkar S, Das DK, Khan AT. Synthesis of fully-substituted pyridines and dihydropyridines in a highly chemoselective manner utilizing a multicomponent reaction (MCR) strategy Rsc Advances. 4: 53752-53760. DOI: 10.1039/C4Ra08237K |
0.415 |
|
2014 |
Das DK, Sarkar S, Khan AT, Saravanan P, Patra S. Synthesis of fused tetrahydropyrido[2,3-c]coumarin derivatives as potential inhibitors for dopamine d3 receptors, catalyzed by hydrated ferric sulfate Rsc Advances. 4: 3581-3590. DOI: 10.1039/C3Ra45174G |
0.399 |
|
2014 |
Islam K, Das DK, Khan AT. Hydrated ferric sulfate catalyzed synthesis of 5,6-unsubstituted 1,4-dihydropyridines using three-component reaction Tetrahedron Letters. 55: 5613-5617. DOI: 10.1016/J.Tetlet.2014.08.067 |
0.327 |
|
2014 |
Bhattacharjee S, Das DK, Khan AT. ChemInform Abstract: Ammonium Chloride-Catalyzed Three-Component Reaction for the Synthesis of Fused 4H-Chromene Derivatives in Aqueous Medium. Cheminform. 45: no-no. DOI: 10.1002/CHIN.201425156 |
0.419 |
|
2014 |
Sarkar S, Das DK, Khan AT. ChemInform Abstract: Sodium-Hydroxide-Mediated Synthesis of Highly Functionalized [1,6]-Naphthyridines in a One-Pot Pseudo Five-Component Reaction. Cheminform. 45: no-no. DOI: 10.1002/CHIN.201411182 |
0.369 |
|
2013 |
Jana N, Das D, Nanda S. Asymmetric total synthesis of 5′-epi-cochliomycin C Tetrahedron. 69: 2900-2908. DOI: 10.1016/J.Tet.2013.02.033 |
0.371 |
|
2013 |
Sarkar S, Das DK, Khan AT. Sodium-Hydroxide-Mediated Synthesis of Highly Functionalized [1,6]-Naphthyridines in a One-Pot Pseudo Five-Component Reaction European Journal of Organic Chemistry. 2013: 6823-6830. DOI: 10.1002/Ejoc.201300894 |
0.354 |
|
2013 |
Khan AT, Das DK, Islam K, Das P. ChemInform Abstract: A Simple and Expedient Synthesis of Functionalized Pyrido[2,3-c] Coumarin Derivatives Using Molecular Iodine Catalyzed Three-Component Reaction. Cheminform. 44: no-no. DOI: 10.1002/CHIN.201312141 |
0.442 |
|
2012 |
Khan AT, Das DK, Islam K, Das P. A simple and expedient synthesis of functionalized pyrido[2,3-c] coumarin derivatives using molecular iodine catalyzed three-component reaction Tetrahedron Letters. 53: 6418-6422. DOI: 10.1016/J.Tetlet.2012.09.051 |
0.464 |
|
2012 |
Khan AT, Das DK. Michael Initiated Ring Closure (MIRC) reaction on in situ generated benzylidenecyclohexane-1,3-diones for the construction of chromeno[3,4-b]quinoline derivatives Tetrahedron Letters. 53: 2345-2351. DOI: 10.1016/J.Tetlet.2012.02.114 |
0.401 |
|
2012 |
Khan AT, Khan MM, Das DK, Lal M. Silica-Supported Perchloric Acid (HClO4-SiO2): An Efficient Catalyst for One-Pot Synthesis of Functionalized Tetrahydropyrimidine Derivatives Journal of Heterocyclic Chemistry. 49: 1362-1369. DOI: 10.1002/Jhet.1017 |
0.412 |
|
2012 |
Khan AT, Das DK. ChemInform Abstract: Michael Initiated Ring Closure (MIRC) Reaction on in situ Generated Benzylidenecyclohexane-1,3-diones for the Construction of Chromeno[3,4-b]quinoline Derivatives. Cheminform. 43: no-no. DOI: 10.1002/CHIN.201234144 |
0.3 |
|
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