An efficient one-pot synthesis of pyrazolyl-thiazolidinedione hybrid analogues and evaluation of their antimicrobial activity

2020 ◽  
Vol 29 ◽  
pp. 100507
Author(s):  
Sivaganesh Tummalacharla ◽  
Pannala Padmaja ◽  
Pedavenkatagari Narayana Reddy
2021 ◽  
Vol 45 (12) ◽  
pp. 5576-5588
Author(s):  
C. Sabarinathan ◽  
M. Karthikeyan ◽  
R. M. Murugappan ◽  
Savarimuthu Philip Anthony ◽  
Bhaskaran Shankar ◽  
...  

One-pot synthesis of POM-salt ([Himi]4[SiMo12O40] (1)) was achieved by mixing silicomolybdic acid and imidazole in acidic conditions and characterized by FTIR, TGA, SEM, EDX, ICP-OES and XPS.


2017 ◽  
Vol 13 (2) ◽  
pp. 6006-6020
Author(s):  
Amira A. El-Sayed ◽  
Maher El-HAshash ◽  
Sameh Rizk

One pot synthesis and reaction of triazinthione and triazinohydrazide derivatives with different electrophilic reagents in ordered to synthesis of some interesting non-mixed heterocyclic compounds. Structures of thiazolotriazine, triazolotriazine, pyrimidinyltriazine, and triazinotriazine derivatives were established via spectroscopic data and elemental analysis. The synthesized compounds were screened for their antimicrobial activity.


2009 ◽  
Vol 24 (5) ◽  
pp. 1095-1100 ◽  
Author(s):  
Kallappa Mahadevappa Hosamani ◽  
Harisha Reddy Seetharamareddy ◽  
Rangappa Sangappa Keri ◽  
Manohar Shirugumbi Hanamanthagouda ◽  
Mark G. Moloney

Author(s):  
Harjinder Singh ◽  
Bhaskara Nand ◽  
Jayant Sindhu ◽  
Jitender M. Khurana ◽  
Chetan Sharma ◽  
...  

2014 ◽  
Vol 51 (S1) ◽  
pp. E146-E151 ◽  
Author(s):  
A. B. V. Kiran Kumar ◽  
A. Uma Ravi Sankar ◽  
Sang Ho Kim

2011 ◽  
Vol 65 (5) ◽  
Author(s):  
Pattusamy Nithya ◽  
Fazlur-Rahman Nawaz Khan ◽  
Selvaraj Roopan ◽  
Uma Shankar ◽  
Jong Jin

AbstractAn efficient and environmentally benign one-pot method for the synthesis of 1-methyl-2,6-diarylpiperidin-4-ones using montmorillonite K-10 as a catalyst has been developed. Antimicrobial activity of the compounds has been tested against selected representatives of Gram-positive and Gram-negative bacteria and fungi.


2019 ◽  
Vol 63 (4) ◽  
Author(s):  
ASHOK DONGAMANTI ◽  
Nagaraju Nalaparaju ◽  
Sarasija Madderla ◽  
Vijaya Lakshmi Bommidi

In the present work, we report the one pot synthesis of tetrazole based 3-hydroxy-4H-chromen-4-ones 3(a-g) from  4-(1H-tetrazol-5-yl)benzaldehyde and 2-hydroxy acetophenone using KOH and H2O2 by modified Algar-Flynn-Oyamada reaction under conventional and microwave irradiation conditions. In this technique, flavonols are synthesized without isolating chalcones, in good yields. All the synthesized compounds were characterized by IR, NMR, MS and elemental. All newly synthesized compounds were screened for their in-vitro antimicrobial activity against strains such as Staphylococcus aurous, Bacillus subtilis, Klebsiella pneumonia, Escherichia coli, Aspergillus Niger, Aspergillus flavus, and Fusarium oxysporum. The results of antimicrobial studies revealed that most of the compounds exhibit good activity.


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