Design, synthesis, and characterization of novel aminoalcohol quinolines with strong in vitro antimalarial activity

Author(s):  
A. Dassonville-Klimpt ◽  
J. Schneider ◽  
C. Damiani ◽  
C. Tisnerat ◽  
A. Cohen ◽  
...  
2009 ◽  
Vol 19 (10) ◽  
pp. 2811-2814 ◽  
Author(s):  
Andrea L. Pelotte ◽  
Ryan M. Smith ◽  
Mario Ayestas ◽  
Christina M. Dersch ◽  
Edward J. Bilsky ◽  
...  

2004 ◽  
Vol 1 (5) ◽  
pp. 228-230 ◽  
Author(s):  
S. R. Dhol ◽  
P. M. Gami ◽  
R. C. Khunt ◽  
A. R. Parikh

Diphenyl aceto hydrazide on reaction with carbon disulfide and potassium hydroxide gave potassiumα,α-diphenyl acetamido dithiocarbamate, which on cyclisation with hydrazine hydrate yielded key intermediate 3-mercapto-4,N-amino-5-benzhydryl-1,2,4-triazoles. The key intermediate on condensation with different acid chloride afforded our titled compounds. The synthesised compounds have been confirmed elemental analyses and further supported by spectral data. All the synthesised compounds have been evaluated for theirin vitroin vitro antimicrobial activity.


RSC Advances ◽  
2016 ◽  
Vol 6 (64) ◽  
pp. 59375-59388 ◽  
Author(s):  
Manjunatha Bhat ◽  
Nagaraja G. K. ◽  
Reshma Kayarmar ◽  
Peethamber S. K. ◽  
Mohammed Shafeeulla R

A new series of 1,2,3-triazolyl pyrazole derivatives were synthesisedviaa Vilsmeier–Haack reaction approach and screened for theirin vitroanti-bacterial, anti-fungal and anti-oxidant activities.


2015 ◽  
Vol 94 ◽  
pp. 45-55 ◽  
Author(s):  
Céline Meinguet ◽  
Céline Bruyère ◽  
Raphaël Frédérick ◽  
Véronique Mathieu ◽  
Christelle Vancraeynest ◽  
...  

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