| Year |
Citation |
Score |
| 2022 |
Yashmin S, Mondal S, Das R, Banerjee P, Khan AT. Regioselective synthetic approach for key precursors of 6-arylbenzo[]phenanthridin-10-ol derivatives: a useful compound for selective chromogenic recognition of fluoride. Organic & Biomolecular Chemistry. PMID 36069360 DOI: 10.1039/d2ob01260j |
0.777 |
|
| 2022 |
Yashmin S, Ali R, Mondal S, Khan AT. DMSO-assisted environmentally benign synthesis of benzo[]-chromeno[4,3,2-]phenanthridines by remote oxidative hetero cross-coupling cyclization and aromatization reaction. Chemical Communications (Cambridge, England). PMID 35467679 DOI: 10.1039/d2cc01067d |
0.801 |
|
| 2021 |
Belal M, Mondal S, Yashmin S, Khan AT. Reactivity switch-over of 4-hydroxydithiocoumarins under various conditions and their application in organic synthesis. Organic & Biomolecular Chemistry. PMID 34950941 DOI: 10.1039/d1ob01357b |
0.701 |
|
| 2021 |
Mondal S, Yashmin S, Khan AT. Synthesis of vinyl sulfides and thioethers a hydrothiolation reaction of 4-hydroxydithiocoumarins and arylacetylenes/styrenes. Organic & Biomolecular Chemistry. PMID 34633026 DOI: 10.1039/d1ob01729b |
0.778 |
|
| 2021 |
Mondal S, Yashmin S, Ali R, Soundaram R, Ghosh SS, Khan AT. Synthesis of biologically active fused 1,4-oxathiin derivatives from 4-hydroxydithiocoumarins, arylacetylenes and dimethyl sulfoxide by Cu(I)-catalyzed C-H functionalization and cross-dehydrogenative C-S coupling reactions. Organic & Biomolecular Chemistry. PMID 34113949 DOI: 10.1039/d1ob00846c |
0.772 |
|
| 2020 |
Mondal S, Mahato K, Arora N, Kankane D, Singh UP, Ali S, Khan AH, Ghosh SS, Khan AT. Newly synthesized 3-sulfenylindole derivatives from 4-hydroxydithiocoumarin using an oxidative cross dehydrogenative coupling reaction (OCDCR): potential lead molecules for antiproliferative activity. Organic & Biomolecular Chemistry. PMID 32432294 DOI: 10.1039/D0Ob00054J |
0.776 |
|
| 2020 |
Ali S, Gattu R, Singh V, Mondal S, Khan AT, Dubey G, Bharatam PV. Reaction behaviour of arylamines with nitroalkenes in the presence of bismuth(iii) triflate: an easy access to 2,3-dialkylquinolines. Organic & Biomolecular Chemistry. PMID 32073090 DOI: 10.1039/C9Ob02214G |
0.778 |
|
| 2019 |
Mondal S, Bera S, Ghosh P. Redox Cascades and Making of a C-C Bond: 1,2-Benzodiazinyl Radicals and a Copper Complex of a Benzodiazine. The Journal of Organic Chemistry. PMID 30663879 DOI: 10.1021/acs.joc.8b02858 |
0.467 |
|
| 2019 |
Mondal S, Yetra SR, Mukherjee S, Biju AT. NHC-Catalyzed Generation of α,β-Unsaturated Acylazoliums for the Enantioselective Synthesis of Heterocycles and Carbocycles. Accounts of Chemical Research. PMID 30653296 DOI: 10.1021/Acs.Accounts.8B00550 |
0.451 |
|
| 2018 |
Gattu R, Mondal S, Ali S, Khan AT. Iodine monobromide catalysed regioselective synthesis of 3-arylquinolines from α-aminoacetophenones and trans-β-nitrostyrenes. Organic & Biomolecular Chemistry. PMID 30548050 DOI: 10.1039/C8Ob02333F |
0.741 |
|
| 2018 |
Kibriya G, Mondal S, Hajra A. Visible-Light-Mediated Synthesis of Unsymmetrical Diaryl Sulfides via Oxidative Coupling of Arylhydrazine with Thiol. Organic Letters. PMID 30484662 DOI: 10.1021/acs.orglett.8b03549 |
0.312 |
|
| 2018 |
Mong KT, Lu YC, Mondal S, Wang CC, Lin CH. Diverse Synthesis of Natural Trehalosamines and Synthetic 1,1'-Disaccharide Aminoglycosides. Chembiochem : a European Journal of Chemical Biology. PMID 30421539 DOI: 10.1002/cbic.201800656 |
0.325 |
|
| 2018 |
Wani IA, Das S, Mondal S, Ghorai MK. Stereoselective Construction of Pyrazinoindoles and Oxazinoindoles via Ring-Opening/Pictet-Spengler Reaction of Aziridines and Epoxides with 3-Methylindoles and Carbonyls. The Journal of Organic Chemistry. PMID 30407006 DOI: 10.1021/Acs.Joc.8B02339 |
0.57 |
|
| 2018 |
Bhattacharyya S, Mondal S, Liu K. Imaging a Resonance-Dominant Polyatomic Reaction: F + CHD → CH(v = 2) + DF(v). The Journal of Physical Chemistry Letters. PMID 30188130 DOI: 10.1021/Acs.Jpclett.8B02517 |
0.364 |
|
| 2018 |
Patra B, Sobottka S, Mondal S, Sarkar B, Kar S. Metal coordination induced ring contraction of porphyrin derivatives. Chemical Communications (Cambridge, England). PMID 30116822 DOI: 10.1039/C8Cc04670K |
0.398 |
|
| 2018 |
Mondal S, Hajra A. Metal-Free C-5 Hydroxylation of 8-Aminoquinoline Amide. The Journal of Organic Chemistry. PMID 30095252 DOI: 10.1021/acs.joc.8b01635 |
0.485 |
|
| 2018 |
Chandra J, Manne SR, Mondal S, Mandal B. ()-Ethyl-2-cyano-2-(((2,4,6-trichlorobenzoyl)oxy)imino)acetate: A Modified Yamaguchi Reagent for Enantioselective Esterification, Thioesterification, Amidation, and Peptide Synthesis. Acs Omega. 3: 6120-6133. PMID 30023940 DOI: 10.1021/acsomega.8b00732 |
0.327 |
|
| 2018 |
Mondal S, Acharya S, Biswas R, Bagchi B, Zare RN. Enhancement of reaction rate in small-sized droplets: A combined analytical and simulation study. The Journal of Chemical Physics. 148: 244704. PMID 29960367 DOI: 10.1063/1.5030114 |
0.402 |
|
| 2018 |
Dhara D, Kalita P, Mondal S, Narayanan RS, Mote KR, Huch V, Zimmer M, Yildiz CB, Scheschkewitz D, Chandrasekhar V, Jana A. Reactivity enhancement of a diphosphene by reversible N-heterocyclic carbene coordination. Chemical Science. 9: 4235-4243. PMID 29780553 DOI: 10.1039/C8Sc00348C |
0.393 |
|
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