Hari Babu Bollikolla

ORCID: 0000-0003-1308-391X
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About
Contact & Profiles
Research Areas
  • Synthesis and biological activity
  • Synthesis and Biological Evaluation
  • Multicomponent Synthesis of Heterocycles
  • Ionic liquids properties and applications
  • Analytical Methods in Pharmaceuticals
  • Catalytic C–H Functionalization Methods
  • Thermodynamic properties of mixtures
  • Analytical Chemistry and Chromatography
  • Synthesis and Characterization of Heterocyclic Compounds
  • Click Chemistry and Applications
  • Nanomaterials for catalytic reactions
  • Graphene and Nanomaterials Applications
  • Sulfur-Based Synthesis Techniques
  • Synthesis of Organic Compounds
  • Synthesis and Catalytic Reactions
  • Chemical and Physical Properties in Aqueous Solutions
  • Antibiotics Pharmacokinetics and Efficacy
  • Chemical Thermodynamics and Molecular Structure
  • Synthesis of Tetrazole Derivatives
  • Cancer therapeutics and mechanisms
  • Chemical Synthesis and Reactions
  • Oxidative Organic Chemistry Reactions
  • Catalytic Cross-Coupling Reactions
  • Marine Sponges and Natural Products
  • Nanoparticles: synthesis and applications

Acharya Nagarjuna University
2016-2025

Andhra University
1993-2024

Acharya N. G. Ranga Agricultural University
2022

National Chung Hsing University
2022

Bridge University
2021

National Institute of Technology Andhra Pradesh
2018

Guntur Medical College
2014-2017

Rayalaseema University
2013

Amala Institute of Medical Sciences
2001-2004

The fresh juice of Rosa damascena Mill. flower exhibited promising in vitro antioxidant potential. partially purified acetone fraction (AF) from silica gel column chromatography was found to be the active with properties. AF required for 50% inhibition superoxide radical production, hydroxyl generation and lipid peroxide formation were 13.75, 135 410µg/ml, respectively. Oral administration at 50mg/kg body weight significantly reduced serum alkaline phosphatase (ALP), glutamine pyruvate...

10.1076/phbi.41.5.357.15945 article EN Pharmaceutical Biology 2003-01-01

Our current work is aimed at synthesizing novel substituted 1,2,4-triazolyl-fluoroquinolone analogs and study of their biological activity to find active promising molecules. The structural elucidation the products was demonstrated by a variety spectroscopic methods such as IR, 1 H-NMR, 13 C-NMR, mass elemental analysis. newly synthesized 1,2,4-triazole derivatives were tested in vitro for ability inhibit growth seven different microbes including S. epidermidis, pneumoniae, aureus, B....

10.1002/cbdv.202201259 article EN Chemistry & Biodiversity 2023-03-16

Abstract Diacetoxyiodobenzene ( PhI OAc ) 2 ), commonly referred to as DAIB or phenyliodine( III diacetate PIDA is one of the most frequently used hypervalent iodines employed an oxidizing agent in organic chemistry. In this review, highlighted exclusively relation its applications synthesis involving heterocyclic ring formations and critically in‐depth examined from summer 2015 present with a specific focus on mechanistic pathway.

10.1002/jhet.4627 article EN Journal of Heterocyclic Chemistry 2023-01-27

Abstract: One of the most widely utilized hypervalent iodines used as an oxidizing agent in organic chemistry is (dialcetoxyiodo)benzene (PhI(OAc)2), also known (DAIB), phenyliodine(III) diacetate (PIDA). In this mini-review, PIDA highlighted relation to its applications synthesis involving rearrangement/migration reactions along with their interesting mechanistic aspects from summer 2015 present.

10.2174/1385272827666230330105241 article EN Current Organic Chemistry 2023-01-01

Abstract Compounds containing fluoroquinolone (FQ) moiety occupy privileged chemical space for discovering novel bioactive substances. In continuation of our research work, a new series FQs linked to triazolyl–thiadiazine hybrids ( 3a–f ) and triazolyl–oxadiazoles 5a–f were developed as antimicrobial agent targeting DNA gyrase Staphylococcus aureus . All the compounds have been characterized with IR, 1 H NMR, 13 C mass spectral analysis elemental analysis. synthesized derivatives...

10.1002/jhet.4700 article EN Journal of Heterocyclic Chemistry 2023-08-21

Substituted 2-aminophenyl benzothiazoles have been constructed from thiourea <italic>via</italic> copper-catalyzed desulfurization/nucleophilic substitution followed by domino intra- and intermolecular C–N cross-coupling reactions under moderate reaction conditions.

10.1039/c8ob02018c article EN Organic & Biomolecular Chemistry 2018-01-01
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