Matiur Rahman
Affiliations: | Visva-Bharati University |
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| Bhattacherjee D, Kovalev IS, Kopchuk DS, et al. (2022) Mechanochemical Approach towards Multi-Functionalized 1,2,3-Triazoles and Anti-Seizure Drug Rufinamide Analogs Using Copper Beads. Molecules (Basel, Switzerland). 27 |
| Bhattacherjee D, Rahman M, Ghosh S, et al. (2021) Advances in Transition‐Metal Catalyzed Carbonylative Suzuki‐Miyaura Coupling Reaction: An Update Advanced Synthesis & Catalysis. 363: 1597-1624 |
| Rahman M, Bagdi AK, Kopchuk DS, et al. (2020) Recent advances in the synthesis of fluorinated compounds an aryne intermediate. Organic & Biomolecular Chemistry |
| Bagdi AK, Rahman M, Bhattacherjee D, et al. (2020) Visible light promoted cross-dehydrogenative coupling: a decade update Green Chemistry. 22: 6632-6681 |
| Rahman M, Mukherjee A, Kovalev IS, et al. (2019) Cover Picture: Recent Advances on Diverse Decarboxylative Reactions of Amino Acids (Adv. Synth. Catal. 10/2019) Advanced Synthesis & Catalysis. 361: 2160-2160 |
| Rahman M, Mukherjee A, Kovalev IS, et al. (2019) Recent Advances on Diverse Decarboxylative Reactions of Amino Acids Advanced Synthesis & Catalysis. 361: 2161-2214 |
| Kopchuk DS, Krinochkin AP, Khasanov AF, et al. (2017) 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 |
| Kopchuk DS, Chepchugov NV, Kovalev IS, et al. (2017) 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 |
| Rahman M, Ling I, Abdullah N, et al. (2015) Organocatalysis by p-sulfonic acid calix[4]arene: a convenient and efficient route to 2,3-dihydroquinazolin-4(1H)-ones in water Rsc Advances. 5: 7755-7760 |
| Rahman M, Bagdi AK, Mishra S, et al. (2014) Functionalization of an sp(3) C-H bond via a redox-neutral domino reaction: diastereoselective synthesis of hexahydropyrrolo[2,1-b]oxazoles. Chemical Communications (Cambridge, England). 50: 2951-3 |