A General Microwave-Assisted Synthesis of Substituted Crown Ethers with Pendant Alkyl or Aryl Ligands

2014 ◽  
Vol 2 (1) ◽  
pp. 5
Author(s):  
Kevin Kittredge ◽  
Justin Malinowski ◽  
Robert Day ◽  
Rachel Courtney ◽  
Stephen McCarron ◽  
...  
2014 ◽  
Vol 11 (2) ◽  
pp. 109-115 ◽  
Author(s):  
Rey Torrejos ◽  
Grace Nisola ◽  
Arnel Beltran ◽  
Myoung Park ◽  
Basavaraj Patil ◽  
...  

ChemInform ◽  
2014 ◽  
Vol 45 (24) ◽  
pp. no-no
Author(s):  
Rey Eliseo C. Torrejos ◽  
Grace M. Nisola ◽  
Arnel B. Beltran ◽  
Myoung Jun Park ◽  
Basavaraj R. Patil ◽  
...  

2020 ◽  
Vol 57 (3) ◽  
pp. 265-272
Author(s):  
Priya S. Singh ◽  
Aizaz Shaikh ◽  
Aditi Deshmukh ◽  
Amit P. Pratap

2013 ◽  
Vol 17 (20) ◽  
pp. 2279-2304 ◽  
Author(s):  
Shrinivas Joshi ◽  
Uttam More ◽  
Venkatrao Kulkarni ◽  
Tejraj Aminabhavi

Author(s):  
Hadis Khodadad ◽  
Farhad Hatamjafari ◽  
Khalil Pourshamsian ◽  
Babak Sadeghi

Aim and Objective: Microwave-assisted condensation of acetophenone 1 and aromatic aldehydes 2 gave chalcone analogs 3, which were cyclized to pyrazole derivatives 6a-f via the reaction with hydrazine hydrate and oxalic acid in the presence of the catalytic amount of acetic acid in ethanol. Materials and Methods: The structural features of the synthesized compounds were characterized by melting point, FT-IR, 1H, 13C NMR and elemental analysis. Results: The antibacterial activities of the synthesized pyrazoles was evaluated against three gram-positive bacteria such as Enterococcus durans, Staphylococcus aureus, Bacillus subtilis and two gram-negative bacteria such as Escherichia coli and Salmonella typhimurium. Conclusion: All the synthesized pyrazoles showed relatively high antibacterial activity against S. aureus strain and none of them demonstrated antibacterial activity against E. coli.


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