INDRAJIT KARMAKAR
National Chung Hsing University, Sido Kanhu Murmu University, Visva-Bharati University
About
Indrajit Karmakar received his B.Sc. (Hons.) in Chemistry and M.Sc. (Organic Chemistry) in 2013 and 2015, respectively, from Visva-Bharati University, India. In 2022, he was awarded his Ph.D. degree in synthetic organic chemistry from Visva-Bharati University under the supervision of Professor (Dr.) Goutam Brahmachari. He is currently pursuing his postdoctoral research with Professor (Dr.) Chin-Fa Lee at National Chung Hsing University, Taiwan. His research interests focus on exploring the applications of green tools in designing and developing novel synthetic methodologies for bio-relevant natural product-like scaffolds.
Employment
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National Chung Hsing University Post-Doctorate2024 - Present
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Sido Kanhu Murmu University Assistant Professor2024 - 2024
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Visva-Bharati University Post-Doctorate2022 - 2024
Education
Education history is unavailable.
Projects & Funding
Projects & funding information is unavailable.
Publications (66)
- Electro‐ and Mechanochemical C(sp2)‐H Chalcogenations of 4‐Hydroxycoumarins/4‐Hydroxy‐N‐methylquinolin‐2‐one: A Dual Green Synthetic Approach Save
- Electrochemical Phosphorochalcogenations for the Synthesis of Phosphorochalcogenothioates Save
- Base‐Promoted Thioester Synthesis from Acyl Fluorides Using Sulfonyl Hydrazides as Thiol Surrogates Save
- Functionalized Diphenyl (2-Oxochroman-4-yl)phosphonates: Dual Synthetic Approaches, Mechanistic Insights, and Exploration of a Promising Anti-Lung Cancerous Molecule Save
- Electrochemical sulfinylation-driven skeletal rearrangement of Baylis–Hillman adducts Save
- Alcohol/Water-Relay Sulfurative Oxygenation of Vinyl Bromides Enabled by Photoinduced EDA Complexes Save
- Visible-light-promoted hydroxysulfenylation of alkenes for the synthesis of β-hydroxysulfides Save
- Transition metal-free stereospecific di-chalcogenations of substituted acetylenes Save
- Sono- and mechanochemical dual syntheses of bio-relevant aryldiazenyl-substituted phosphine oxides/phosphonates via P(O)–H functionalisation Save
- Palladium-catalyzed reductive cross-coupling reaction of carboxylic acids with thiols: an alternative strategy to access thioesters Save