0974-4150 (Online)
0974-4169 (Print)

Author(s): N.P. Lachoriya, Dilesh Indorkar, S.P. Shrivastava, O.P. Chourasia, S.N. Limaye


DOI: Not Available

Address: N.P. Lachoriya, Dilesh Indorkar, S.P. Shrivastava, O.P. Chourasia and S.N. Limaye
Department of Chemistry, Dr. H. S. Gour Central University, Sagar (M.P.)-470003
*Corresponding Author

Published In:   Volume - 5,      Issue - 9,     Year - 2012

The recent synthesis of 1-(aryl substituted)–3–(4'-Bromo phenyl) Prop–1–ene–3–ones prepared by p–bromo acetophenone (1 mol.) in ethanol (25 ml), aromatic aldehyde reaction 01 the solution was added 3–(4'-Bromo phenyl)-5–(aryl substituted) isoxazoles sodium acetate (0.01 mol.) dissolved in a minimum amount of hot glacial acetic acid was added to a solution of NH2OH.HCl (0.01 mol) in ethanol (10 ml). This solution was added to a solution of 1-(aryl substituted) -3-(4'-Bromophenyl) prop-1-ene–3–one.1-(aryl substituted)-3-(4'-Bromophenyl)-pop-1-ene-3-ones (0.01 mol), NH2OH.HCl (0.02 mol) and KOH (0.02 mol) in ethanol (25 ml) were refluxed on water bath for four hours. The reaction mixture was then cooled and acidified with glacial acetic acid. The resulting solid was washed with water and recrystallized from rectified spirit new compounds was 3-(4'-Bromo phenyl)-5-(aryl substituted) isoxazolines. respectively. Analysis in the PC-model values and Antibacterial , Antifungal activity This new route of synthesis has been proposed.

Cite this article:
N.P. Lachoriya, Dilesh Indorkar, S.P. Shrivastava, O.P. Chourasia, S.N. Limaye. Synthesis of 3-(4'-Bromo phenyl)-5-(aryl substituted) isoxazolines Compounds computational studies and Biological activity. Asian J. Research Chem. 5(9): September, 2012; Page 1095-1098.

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RNI: Not Available                     
DOI: 10.5958/0974-4150 

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