Swadhin Chetia

ORCID: 0000-0002-1355-9271
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About
Contact & Profiles
Research Areas
  • Quinazolinone synthesis and applications
  • Catalytic C–H Functionalization Methods
  • Multicomponent Synthesis of Heterocycles
  • Click Chemistry and Applications
  • Phenothiazines and Benzothiazines Synthesis and Activities
  • Microwave-Assisted Synthesis and Applications
  • Chemical Synthesis and Analysis
  • Advanced Synthetic Organic Chemistry
  • Synthesis and Biological Evaluation
  • Asymmetric Hydrogenation and Catalysis
  • Chemistry and Chemical Engineering

Dibrugarh University
2021-2025

An environmentally benign protocol has been developed for the synthesis of two biologically important N-heterocycles i.e. 2,3-dihydroquinazolin-4(1H)-ones and NH-1,2,3-triazoles. These N-heterocyclic compounds are synthesized by readily available inexpensive LiClO4 in ethylene glycol (EG) PEG-400 with good to excellent product yield providing an benchmark rapid these heterocycles under operational simplicity. Sc-XRD one products gives structural information DFT calculations provide on...

10.1055/a-2532-7424 article EN Synlett 2025-02-04

Regioselective synthesis of 1,2,3-triazoles has emerged as a cornerstone modern synthetic chemistry, offering immense potential in pharmaceuticals, materials science, and functional applications. This account focuses on advancing click reaction, with majority the innovations stemming from our group’s contributions. Highlights include development novel catalytic systems, both homogeneous heterogeneous exploration copper-free photocatalytic methodologies. bridges traditional approaches,...

10.1055/a-2564-4826 article EN Synlett 2025-03-21

Abstract A copper acetate monohydrate catalyzed simple, effective and economic protocol has been developed for the construction of quinazoline derivatives via acceptorless dehydrogenative coupling easily available 2‐aminoaryl methanols nitriles. The methodology was also highly synthesis medicinally important quinolines analogues. reactions proceeded in presence KO t Bu toluene at 110 °C 5 h without requirement inert condition, external additives ligands.

10.1002/ejoc.202300390 article EN European Journal of Organic Chemistry 2023-05-08

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10.2139/ssrn.4773916 preprint EN 2024-01-01
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