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M

M. Rani

Researcher at Annamalai University

Publications -  18
Citations -  222

M. Rani is an academic researcher from Annamalai University. The author has contributed to research in topics: Piperidine & Proton NMR. The author has an hindex of 7, co-authored 18 publications receiving 194 citations.

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Synthesis, spectral, crystal structure and in vitro antimicrobial evaluation of imidazole/benzotriazole substituted piperidin-4-one derivatives.

TL;DR: Imidazole/benzotriazole analogues substituted piperidin-4-one derivatives (17-26) have been synthesized and their chemical structures were characterized by IR, 1H NMR, 13C NMR and mass spectral analysis.
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Design, synthesis and biological evaluation of novel 2-[(2,4-diaryl-3-azabicyclo[3.3.1]nonan-9-ylidene)hydrazono]-1,3-thiazolidin-4-ones as a new class of antimicrobial agents.

TL;DR: These studies proved that compounds 11/18/20/23 against Staphylococcus aureus, 19/ 20/24 against Salmonella typhi show maximum inhibition potency at low concentration whereas 18/19 against Candida albicans and 19/20-21 against Rhizopus sp.
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A facile synthesis and characterization of semiconducting p-phenylenediamine–aniline copolymer

TL;DR: In this paper, the synthesis of p -phenylenediamine ( p -PDA)-aniline copolymer was carried out using K 2 S 2 O 8 and (NH 4 ) 2 S O 8 as an oxidizing agent and the newly synthesized copolymers was characterized by UV-visible, FT-IR, fluorescence, proton NMR, cyclic voltammetry, solubility and SEM studies.
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Design and synthesis of novel piperazine unit condensed 2,6-diarylpiperidin-4-one derivatives as antituberculosis and antimicrobial agents

TL;DR: Among the synthesized compounds, compounds 3e–3j exhibit higher inhibition potency against M. tuberculosis H37Rv and compounds containing fluoro substituent in the phenyl ring at C-2 and C-6 positions of the piperidin-4-one motif exerted better antibacterial and antifungal activity than the other phenyl-substituted compounds.
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Efficient synthesis, spectral analysis and antimicrobial studies of nitrogen and sulfur containing spiro heterocycles from 2,4-diaryl-3-azabicyclo[3.3.1]nonan-9-ones.

TL;DR: The microbiological analysis showed that the electron withdrawing function substituted phenyl group at C-2 and C-4 of azabicyclononane based thiadiazoles 4c/4h and 5c/5h exposed significant antimicrobial activity against Salmonella typhi, Escherichia coli, Klebsiella pneumoniae, Aspergillus flavus, As pergillus niger and Candida albicans.