K. A. Aravinda Kumar

ORCID: 0009-0007-4008-9424
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About
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Research Areas
  • Chemical Synthesis and Reactions
  • Chemical Synthesis and Analysis
  • Catalytic C–H Functionalization Methods
  • Catalytic Cross-Coupling Reactions
  • Asymmetric Hydrogenation and Catalysis
  • Synthesis and biological activity
  • Nanoparticles: synthesis and applications
  • Vanadium and Halogenation Chemistry
  • Metal-Organic Frameworks: Synthesis and Applications
  • Adsorption and biosorption for pollutant removal
  • Mercury impact and mitigation studies
  • Nanomaterials for catalytic reactions
  • Synthesis and Catalytic Reactions
  • Pigment Synthesis and Properties
  • Oxidative Organic Chemistry Reactions
  • PI3K/AKT/mTOR signaling in cancer
  • Magnesium Oxide Properties and Applications
  • Peptidase Inhibition and Analysis
  • Gold and Silver Nanoparticles Synthesis and Applications
  • Cyclopropane Reaction Mechanisms
  • Glass properties and applications
  • Synthesis and Biological Evaluation
  • Computational Drug Discovery Methods
  • Geochemistry and Elemental Analysis
  • Synthesis of heterocyclic compounds

GITAM University
2025

Birla Institute of Technology and Science, Pilani
2020-2024

Council of Scientific and Industrial Research
2012-2019

National Aerospace Laboratories
2019

Indian Institute of Integrative Medicine
2012-2018

University of Jammu
2014-2018

A novel simple, mild chemo- and regioselective method has been developed for the halogenation of phenols using Cu–Mn spinel oxide as a catalyst N-halosuccinimide halogenating agent. In presence B, both electron-withdrawing electron-donating groups bearing gave monohalogenated products in good to excellent yields with highest para-selectivity. The para-substituted phenol product yield ortho-selectivity. N-Heteroarenes such indoles imidazoles also high selectivity. Unlike copper-catalyzed...

10.1021/jo300731z article EN The Journal of Organic Chemistry 2012-06-06

This paper develops models of the Zagreb index suitable for unsaturated fatty acids, which are crucial in performing metabolic functions all living organisms. An algorithm-based methodology was brought into practice to optimize computation and data processing. Degree-based topological indices derived from M-polynomial were computed using SPSS. Using linear regression analysis, study proved that these relevant some physical properties acids. The QSPR (Quantitative Structure-Property...

10.13005/ojc/410124 article EN Oriental Journal Of Chemistry 2025-02-28

The synthesis of tri-substituted pyrazoles was achieved <italic>via</italic> direct N-heterocyclization hydrazines with metal-acetylacetonate and -dibenzylideneacetonate without using any base or additives under microwave irradiation in a single step.

10.1039/c8ra04550j article EN cc-by-nc RSC Advances 2018-01-01

Herein, we report a new method for synthesis of amides and hydroxamic acids directly from nitroarenes aldehydes.

10.1039/c4ob01155d article EN Organic & Biomolecular Chemistry 2014-01-01

Sustainable and eco-friendly MOF–GO functionalized composites demonstrated high adsorption capacity for dye removal from wastewater, offering an environmentally friendly solution.

10.1039/d4ew00185k article EN cc-by-nc Environmental Science Water Research & Technology 2024-01-01

Abstract A novel method for the selective ortho‐directed monohydroxylation and concomitant N‐trifluoroacylation of 2‐ 6‐fluoro‐ or 2,6‐difluoro‐substituted anilines is developed.

10.1002/chin.201540084 article EN ChemInform 2015-09-17

Abstract The title method furnishing amides in excellent yields can be carried out under microwave irradiation as well conventional heating conditions.

10.1002/chin.201547067 article EN ChemInform 2015-11-01

Abstract With AcOH in CHCl 3 amides are obtained as only products, whereas the use of KOH gives predominantly corresponding hydroxamic acid.

10.1002/chin.201504077 article EN ChemInform 2015-01-01

Abstract In the presence of Cu—Mn spinel oxide B and appropriate N‐halosuccinimides, both phenols bearing electron‐withdrawing or electron‐donating groups, as well N‐heteroarenes give monochlorinated monobrominated products with excellent regioselectivities (74‐90%).

10.1002/chin.201244044 article EN ChemInform 2012-10-04
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