Conventional and Microwave Assisted Synthesis with Antimicrobial Evaluation of Novel Pyrrolidine Molecule: An Approach to Easy Synthetic Pathway

2018 ◽  
Vol 8 (2) ◽  
pp. 298-303
Author(s):  
K Sreekanth ◽  
Anjali Jha
Keyword(s):  
Microwave Assisted Synthesis ◽  
Synthetic Pathway ◽  
Microwave Assisted ◽  
Antimicrobial Evaluation

Microwave‐Assisted Synthesis, Antioxidant, and Antimicrobial Evaluation of Piperazine‐Azole‐Fluoroquinolone Based 1,2,4‐Triazole Derivatives

2018 ◽  
Vol 55 (12) ◽  
pp. 2744-2759 ◽  
Author(s):  
Serap Basoglu Ozdemir ◽  
Neslihan Demirbas ◽  
Ahmet Demirbas ◽  
Faik Ahmet Ayaz ◽  
Nesrin Çolak
Keyword(s):  
Microwave Assisted Synthesis ◽  
Triazole Derivatives ◽  
Microwave Assisted ◽  
Antimicrobial Evaluation

scholarly journals Microwave Assisted Synthesis and Antimicrobial Evaluation of Schiff Bases of Indole-3-aldehyde

2011 ◽  
Vol 8 (1) ◽  
pp. 305-311 ◽  
Author(s):  
Priyanka Kamaria ◽  
N. Kawathekar ◽  
Prerna Chaturvedi
Keyword(s):  
Schiff Bases ◽  
Antimicrobial Agents ◽  
Microwave Assisted Synthesis ◽  
Bacterial Strains ◽  
Mass Spectral Analysis ◽  
Gram Positive ◽  
Gram Negative ◽  
Mass Spectral ◽  
Microwave Assisted ◽  
Antimicrobial Evaluation

In order to develop new antimicrobial agents, a series of Schiff bases of indole-3-aldehyde were synthesized by microwave assisted synthesis by takingDMFas solvent and evaluated for their antimicrobial activity. All the synthesized compounds were characterized byIR,1HNMRand mass spectral analysis. All compounds were tested against five gram positive and five gram negative bacterial strains and one fungal strain. All compounds exhibited better activity against gram positive strains than against gram negative strains and the compounds were found more active againstS.aureusandB.subtilis.

Microwave-assisted synthesis, antioxidant and antimicrobial evaluation of 2-indolinone-based bis-1,2,3-triazole derivatives

2017 ◽  
Vol 22 (1) ◽  
pp. 57-70 ◽  
Author(s):  
Dongamanti Ashok ◽  
Srinivas Gundu ◽  
Vikas Kumar Aamate ◽  
Mohan Gandhi Devulapally
Keyword(s):  
Microwave Assisted Synthesis ◽  
Triazole Derivatives ◽  
Microwave Assisted ◽  
Antimicrobial Evaluation

scholarly journals MICROWAVE ASSISTED SYNTHESIS, SPECTRAL CORRELATION AND ANTIMICROBIAL EVALUATION OF SOME ARYL IMINES

2018 ◽  
Vol 63 (2) ◽  
pp. 3918-3923
Author(s):  
S Pazhinivel Sakthinathan ◽  
Ramamoorthy Suresh ◽  
Dakshnamoorthy Kamalakkannan ◽  
Veerandiran Mala ◽  
Kaliyan Sathiyamoorthi ◽  
...  
Keyword(s):  
Microwave Assisted Synthesis ◽  
Spectral Correlation ◽  
Microwave Assisted ◽  
Antimicrobial Evaluation

scholarly journals Microwave - Assisted Synthesis of a Library of Pyrrolo[1,2-c]quinazolines

2019 ◽  
Vol 70 (9) ◽  
pp. 3094-3099 ◽  
Author(s):  
Emilian Georgescu ◽  
Florea Dumitrascu ◽  
Florentina Georgescu ◽  
Constantin Draghici ◽  
Denisa Dumitrescu
Keyword(s):  
Large Range ◽  
Dipolar Cycloaddition ◽  
Microwave Assisted Synthesis ◽  
One Pot ◽  
Synthetic Pathway ◽  
Microwave Assisted ◽  
Rapid Access ◽  
Quinazoline Derivatives ◽  
The One

A library of new pyrrolo[1,2-c]quinazoline derivatives was obtained by the one-pot, three-component microwave-assisted synthesis, starting from quinazolines, 2-bromoacetyl derivatives and electron-deficient alkynes in 1,2-epoxybutane via 1,3-dipolar cycloaddition of quinazolinium N-ylides. This synthetic pathway offers a simple and rapid access to a large range of pyrrolo[1,2-c]quinazoline derivatives.

scholarly journals Microwave-assisted synthesis and antimicrobial evaluation of 6-[3-aryl-1-phenyl-4’,5’-dihydro[4,5’-bi-1H-pyrazol]-3’-yl]-2H-chromen-5-ols

2019 ◽  
Vol 84 (3) ◽  
pp. 237-244
Author(s):  
Dongamanti Ashok ◽  
Rangu Kavitha ◽  
Srinivas Gundu ◽  
Madderla Sarasija
Keyword(s):  
Antimicrobial Activity ◽  
Microwave Irradiation ◽  
Sodium Acetate ◽  
Analytical Data ◽  
Conventional Heating ◽  
Microwave Assisted Synthesis ◽  
Microwave Assisted ◽  
Structural Assignment ◽  
Antimicrobial Evaluation ◽  
Antimicrobial Potency

A new series of 6-[3-aryl-1-phenyl-4?,5?-dihydro[4,5?-bi-1H-pyrazol]-3?-yl]-2H-chromen-5-ol derivatives was synthesized by Michael addition of chalcones 5a?j with hydrazine hydrate in presence of sodium acetate under conventional heating and microwave irradiation. Structural assignment of the products was confirmed based on IR, 1H-NMR, 13C-NMR, MS and analytical data. All the synthesized compounds 6a?j were screened for their antimicrobial activity against various bacterial and fungal strains. Most of the compounds exhibited variable range of antimicrobial activity and compounds 6c?f and 6i showed promising antimicrobial potency.

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