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Synthesis of vinyl sulfides and thioethers a hydrothiolation reaction of 4-hydroxydithiocoumarins and arylacetylenes/styrenes
Organic & biomolecular chemistry, 2021-11, Vol.19 (42), p.9223-923
2021
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Synthesis of vinyl sulfides and thioethers via a hydrothiolation reaction of 4-hydroxydithiocoumarins and arylacetylenes/styrenes
Organic & biomolecular chemistry, 2021-11, Vol.19 (42), p.9223-9230
2021
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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), 2022-05, Vol.58 (39), p.5853-5856
2022
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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, 2022-09, Vol.2 (36), p.732-7315
2022
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Reactivity switch-over of 4-hydroxydithiocoumarins under various conditions and their application in organic synthesis
Organic & biomolecular chemistry, 2022-01, Vol.2 (4), p.715-726
2022
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Regioselective Ring‐Opening of Epoxide and N‐Tosylaziridine with 4‐Hydroxydithiocoumarin: Key Precursors for 2,3‐Dihydro‐1,4‐oxathiin and 2,3‐Dihydro‐1,4‐thiazine Derivatives
European journal of organic chemistry, 2022-05, Vol.2022 (18), p.n/a
2022
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Iodine monobromide catalysed regioselective synthesis of 3-arylquinolines from α-aminoacetophenones and trans-β-nitrostyrenesElectronic supplementary information (ESI) available. CCDC 1835007 for compound 3h. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c8ob02333f
2019-01
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Iodine monobromide catalysed regioselective synthesis of 3-arylquinolines from α-aminoacetophenones and trans-β-nitrostyrenes
Organic & biomolecular chemistry, 2019-01, Vol.17 (2), p.347-353
2019
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Unconventional sulfur transfer behaviour of 4-hydroxy-dithiocoumarin: an easy access to biologically potent 1,2-dithiolane scaffolds
New journal of chemistry, 2023-01, Vol.47 (4), p.1954-1961
2023
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Synthesis of biologically active fused 1,4-oxathiin derivatives from 4-hydroxydithiocoumarins, arylacetylenes and dimethyl sulfoxide by Cu()-catalyzed C-H functionalization and cross-dehydrogenative C-S coupling reactions
Organic & biomolecular chemistry, 2021-07, Vol.19 (26), p.5818-5826
2021
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Correction: Unconventional sulfur transfer behaviour of 4-hydroxy-dithiocoumarin: an easy access to biologically potent 1,2-dithiolane scaffolds
New journal of chemistry, 2023-01, Vol.47 (5), p.2682-2682
2023
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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, 2020-06, Vol.18 (21), p.414-4113
2020
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Reaction behaviour of arylamines with nitroalkenes in the presence of bismuth() triflate: an easy access to 2,3-dialkylquinolines
Organic & biomolecular chemistry, 2020-03, Vol.18 (9), p.1785-1793
2020
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67P Efficacy and safety of trastuzumab biosimilar in HER2+ve metastatic breast cancer: A multicenter phase III study
Annals of oncology, 2023-11, Vol.34, p.S1491
2023
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Synthesis and biological characterization of an orally bioavailable lactate dehydrogenase-A inhibitor against pancreatic cancer
European journal of medicinal chemistry, 2024-09, Vol.275, p.116598, Article 116598
2024
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Serum creatine kinase and other profile of duchenne muscular dystrophy and becker muscular dystrophy: A cross-sectional survey in a tertiary care institution at Kolkata
Chrismed journal of health and research, 2021-07, Vol.8 (3), p.175-181
2021
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VopF, a type III effector protein from a non-O1, non-O139 Vibrio cholerae strain, demonstrates toxicity in a Saccharomyces cerevisiae model
Journal of medical microbiology, 2010-01, Vol.59 (1), p.17-24
2010
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Bridging the Industry–Academia Gap: An Experiential Learning for Engineering Students
Journal of formative design in learning, 2023-12, Vol.7 (2), p.139-157
2023
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