scholarly journals Regioselective Synthesis of Some Thio Analogues of Quinolone Antibacterials via Borate Complex of Quinolone Carboxylic Acid Catalyzed by DABCO under Microwave Irradiation

ChemInform ◽  
2006 ◽  
Vol 37 (6) ◽  
Author(s):  
Majid M. Heravi ◽  
Zeinab S. Jaddi ◽  
Hossein A. Oskooie ◽  
Shahnaz Khaleghi ◽  
Mitra Ghassemzadeh

2008 ◽  
Vol 62 (6) ◽  
Author(s):  
Zheng Li ◽  
Jing Liu ◽  
Xue Gong ◽  
Xuerong Mao ◽  
Xiunan Sun ◽  
...  

AbstractSilica sulfuric acid was found to be an efficient, recoverable, reusable and environment-friendly catalyst for the fast hydrolysis of various carboxylic acid esters in high conversions and selectivities under microwave irradiation conditions. This protocol has the advantages of no corrosion, no environmental pollution, high reaction rate, high yield, and simple work-up procedure.


2005 ◽  
Vol 2005 (9) ◽  
pp. 578-579 ◽  
Author(s):  
Majid M. Heravi ◽  
Zeinab S. Jaddi ◽  
Hossein A. Oskooie ◽  
Shahnaz Khaleghi ◽  
Mitra Ghassemzadeh

1-substituted 7-chloro-6-fluoro-4-oxo-1,2-dihydroquinoline-3-carboxylic acids were converted to borate complexes. These compounds were treated with piperazine in presence of triethylamine to afford ciprofloxacin and norfloxacin in high yields.


Molbank ◽  
10.3390/m1214 ◽  
2021 ◽  
Vol 2021 (2) ◽  
pp. M1214
Author(s):  
Pablo E. Romo ◽  
Braulio Insuasty ◽  
Jairo Quiroga ◽  
Rodrigo Abonia

3′-methyl-2-oxo-1′,5′-diphenyl-1′,7′-dihydrospiro[indoline-3,4′-pyrazolo[3,4-b]pyridine]-6′-carboxylic acid was synthesized using diverse conditions. The best reaction condition consisted of using water as solvent under microwave irradiation, affording product in 76% yield.


2016 ◽  
Vol 14 (20) ◽  
pp. 4571-4575 ◽  
Author(s):  
Tao Chen ◽  
Ying-Yeung Yeung

A trifluoroacetic acid catalyzed highly 6-endo regioselective bromocyclization of styrene-type carboxylic acid has been developed.


2003 ◽  
Vol 68 (10) ◽  
pp. 723-727 ◽  
Author(s):  
Vijay Dabholkar ◽  
Rahul Gavande

A series of 1-(3,4-dihydro-3-oxo-2H-1,4-benzoxazine-2-carbonyl)-3-methyl-4-(substituted phenylhydrazono)-2-pyrazolin-5-ones have been synthesized by the reaction of 2H-3,4-dihydro-3-oxo-1,4-benzoxazine-2-carboxylic acid hydrazide with substituted acetoacetic ester derivatives using acetic acid as solvent under microwave irradiation (MWI), as well as by conventional methods. The reaction rate is enhanced tremendously and the yields are improved under MWI as compared to conventional methods.


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